Proclinical have partnered with a small Pharma company expanding into the UK and are looking for an experienced Clinical Contracts Analyst to join their growing team. You will work closely with the senior team to lead the analyses of request for proposals from a variety of different vendors in early phase development whilst also managing the full lifecycle of vendor contracts.

This is a great opportunity for someone to work closely with the senior leadership team and take on a wide range of responsibilities

Job Responsibilities

• Work closely with project teams to determine appropriate terms and conditions of contracts
• Develop and prepare Contracts
• Primary customer interface on large, complex contracts, responsible for developing and maintaining customer relationships
• Revise or develop the contracts and related budgets and scope of work. Ensure the scope of work is defined correctly and budgets

To Apply

ProClinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies.

#LI-TN1

Industries:

A global pharmaceutical organisation have an exciting job opening for a Lead Clinical Data Manager to be based in the UK on a contract basis. This Lead Clinical Data Manager role will take responsibility for the development of the project documentation, system set-up, data entry and data validation procedures and processes assigned to more junior staff. Also assume responsibility for all data management activities leading to database lock according to client quality expectations, within project timelines and budgets.

Job Responsibilities

• Lead study Data Manager for studies which are highly complex including but not limited to - combination of healthy volunteer and patient populations, multi-site, complex protocol design, strong client management required or reduced timelines.
• As the study data lead/Client programme lead; be accountable for all DM deliverables as assigned per the established timeline; providing instruction to their DM study team(s) and review of their study team's output to ensure the highest quality, while adjusting resource allocations accordingly.
• Ensure that all allocated projects are carried out in strict accordance with the relevant protocols, global harmonized SOPs, and the specified standards of GCPs.
• Work with the Project Manager(s) to build timelines to meet contracted milestones by communicating with leads in different disciplines and the full project team as necessary, including at study initiation meetings
• Develop and maintain client relationships and review client satisfaction surveys. Implement appropriate action plans including driving process improvements and team training.
• Applies corrective interventions where necessary to maintain project budget compliance and profit expectations. Track scope changes and work with the Clinical Pharmacology Project Manager to ensure that Sponsor approval is received and the scope change processed.
• Provides leadership, mentorship, and coaching in DM related clinical trial processes, department technical capabilities, and associated turnaround durations.
• Coordinates with the DM Global Trainer and DM technology SMEs to coach and mentor study members on DM technologies and best practices for DM applications/tasks such as (EDC execution, SOP forms completion, tracking tools, reviewing vendor data in SAS Viewer, data listings creation, data cleaning).

Skills and Requirements

• University/college degree (life science, pharmacy or related subject preferred)
• ​​​​​​​Extensive hands on Lead DM experience with focus on managing large, phase III studies.
• Excellent understanding and experience in the analysis of protocol amendments to assess the impact on a clinical trial, production of technical DM specifications to drive CRF and database change.
• Skilled at advanced planning and management of multiple elements of a phase III trial
• Oversight, leadership and escalation point for supporting DM team, CRF Developers and Database Programmers.
• Working directly with clients, experience in monitoring DM hours vs budget
• Confident in making key study decisions and producing audit ready documentation to support these

To Apply

ProClinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies.

#LI_SB1

Industries:

An exciting opportunity has arisen for a TMF Manager to be responsible for all Clinical Operations. You will be expecting to work collaboratively with colleagues, external partners to contribute to effective eTMF Management.

Job Responsibilities

• Oversight and management of end-to-end activities to ensure that all OBG study eTMFs are of the highest quality, audit & inspection ready and meet all applicable regulations and guidelines
• Active engagement and communication with Eisai functions and CRO stakeholders to ensure awareness of requirements, interpret metrics and drive timely TMF management
• Collaboration and liaison with Eisai's central TMF Management function on TMF business processes, including continuous improvement activities, training and metrics

Skills and Requirements

• Education to B.Sc. level or equivalent
• Demonstrated experience in the pharmaceutical industry, in Document Management, TMF Management or Clinical Development/Operations, with in-depth knowledge and experience of eTMF process and clinical documentation
• Proven experience with Electronic Clinical Document Management and eTMF systems and knowledge of eTMF requirements and technologies to support document collection and archiving
• Experience in interpreting and communicating KPI metrics and eTMF system reports for study team members and functional leadership
• Must possess excellent organizational and time management skills
• Ability to work both independently and as part of a team within a matrix environment
• Must have strong analytical and problem-solving skills
• Proficient in the use of information technology, especially eTMF and Electronic Document Management systems

To Apply

ProClinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies.

#LI_JO1

Industries:

A vacancy has become available for a talented Senior Associate, Global Clinical Trial Transparency (GCTT). In this role you will perform all aspects of this global Pharmaceutical company's Global Clinical Trial Transparency operations as directed. To ensure compliance with the processes which support the Policy for Clinical Trial Transparency and applicable regulations. Demonstrate success in working collaboratively and independently as required, with internal and external team members to ensure Global Clinical Trial Transparency responsibilities are achieved.

Skills and Requirements

• Education to B.Sc. level or equivalent
• Good knowledge of clinical trial transparency principles for preparation and sharing of patient-level data and PhRMA/EFPIA principles for responsible data sharing, etc.
• Demonstrated experience in the pharmaceutical industry, with exposure to least one of the following areas.
  • Clinical trial transparency
  • Clinical trial disclosure
  • Medical Writing
• Experience supporting and managing tasks / projects, by establishing strong relationships and coordinating those resources (internal and external) to achieve deliverables in compliance with process and / or contract.
• Understanding of clinical development within the pharmaceutical industry.
• Experience of working with different software packages and platforms.

To Apply

ProClinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies.

#LI_JO1

Industries:

An exciting opportunity has arisen for a Local Trial Manager to join a well-established pharmaceutical company. You will ensure that local trial team is delivering quality data and trial documents. You will be expected to lead these services ensuring compliance and quality.

Job Responsibilities

• Contribute to quality Site Selection through participation in site feasibility ensuring consistent conduct of pre trial assessment visits and appropriate follow up of pretrial visit report and country feasibility report.
• Collaborates with central study team for final selection of sites to participate in trial.
• Ensures local/country team is meeting recruitment targets with high quality data on time and within study budget by providing input to study level documents and leading/coordinating local team activities in compliance with SOPs, other procedural documents and applicable regulations.
• Act as primary company contact for assigned trial at the country level, may attend/participate in Investigator Meetings as needed. May schedule and conduct a local/country investigator meeting.
• Contribute to site level recruitment strategy and contingency planning and implementation in partnership with other functional areas to achieve clinical research target.
• Delivers competent vendor management at the country level to support the study and may submit requests for vendor services and support vendor selection. This includes reviewing and approving site and local vendor invoices as required. As required, manages the local study supply.
• Ensures high standards for study monitoring by conducting quality local trial team meetings and facilitating SM training, when needed (i.e. implementation of study amendment and changes in study related processes).
• Contributes to patient understanding of protocol and patient safety by preparing country specific informed consent in accordance with procedural document/templates. This includes reviewing and managing site specific informed consent forms in accordance with SOPs, other procedural documents and applicable regulations.
• With focus on quality, will work closely with SM to ensure CAPA is implemented for audits/inspections or any quality related visits. May conduct accompanied site visits with SM, if delegated by FM.
• Ensure accurate finance reporting and trial delivered within budget by adhering to finance reporting deliverables and timelines. This includes forecasting and proactive management of country/local trial budget. If applicable, may assist in negotiation of trial site contracts and budgets.

Skills and Requirements

• BA/BS degree in a health or science related field.
• 2 years of local trial management experience.
• 3 to 5+ years of trial management experience.
• Specific therapeutic area experience may be required depending on the position.
• Strong working knowledge of ICH GCP, company standard operating procedures, local laws and regulations, assigned protocols and associated protocol specific procedures.
• Strong IT skills in appropriate software and company systems.
• Proficient in speaking and writing the country language and English. Good written and oral communication skills as appropriate.

To Apply

ProClinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies.

#LI_RI1

Industries:

A fantastic vacancy has become available for a Senior Regulatory Consultant in Surrey. This pharmaceutical regulatory affairs job is an excellent opportunity to work for a global leader in the life sciences industry.

Job Responsibilities

• Provide regulatory input to commercial strategic and operating planning process.
• Attend relevant product team meetings with cross-divisional colleagues to provide technical guidance and support for teams as necessary.
• Work with above country regulatory strategists (AC-RS) to provide country input into Global and European Regulatory Strategies as required.
• Seek to improve alignment of local and regional regulatory strategy and tactics.
• Use expert knowledge of EU/national legislation, guidelines, regulatory environment to provide insightful responses to enquiries from cross-divisional colleagues and direct or indirect interactions with external customers.
• Manage and Submit Marketing Authorisation Applications: National/MRP/Decentralised MAA:
• Manage and Submit MA Variation Applications
• Prepare agreed Module 1 documents in partnership with above-country operational hubs. Lead MRP/DCP submission review and planning where country is RMS, in conjunction with AC-RS
• Proactively take opportunities to develop or enhance working relationships with Regulatory Authorities and trade associations.
• Manage Clinical Trial Approvals (if performed in country

Skills and Requirements

• Life sciences or chemistry graduate to honours level or equivalent
• Master's Degree, Post Graduate Diploma or PhD preferred
• Relevant Professional Qualifications desirable, (e.g. MSc in Regulatory Affairs)
• Previous experience and proven track record in Regulatory Affairs (Human Medicinal Products)
• Member of The Organisation for Professionals in Regulatory Affairs (TOPRA) preferred

To Apply

ProClinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies.

#LI-PD1

Industries:

A life-changing role has arisen for a Bioprocess Engineer in Cambridge. You will be working in a talented and dynamic team to address the global challenges.

As a head of process engineering, you will oversee the design of our bioreactors, modelling of our process and scale up to pilot plant. You will be responsible for designing and execute experiments in bioreactors including process and media optimisation. You will develop, plan and coordinate engineering projects, continuously improving on project execution. You will work closely with the rest of our founding team, advisors and partners to ensure that the R&D process is robust and scalable.

Skills and Requirements

• Experience in process development or cell/gene therapy technology development /engineering.
• Chemical Engineering / Bioengineering MEng/MS
• Understanding of GMP and relevant ISO standards.
• Experience in designing and operating bioreactors
• Stem cell/mammalian cells bio-processing experience, induced pluripotent stem cell experience is a plus
• Experience in startups or novel projects
• Experience with computer simulations
• Experience working with CROs
• PhD in relevant subject
• Maker, builder, do-er, relentless pursuer of knowledge
• Flexibility as new challenges and opportunities arise
• Ability to have fun and inspire team members to enjoy work, be action-oriented and stretch their imagination.

To Apply

ProClinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies.

#LI_DC1

Industries:

An exciting opportunity has arisen for a Global Brand Manager to join a success pharmaceutical company in North London. You will be able to support development and implementations of marketing programs. The chosen candidate will assist in designing, implementing and evaluating promotional activities; work in a matrix environment by managing relationships with external agencies and championing brand strategies.

Job Responsibilities

• Plan, identify, develop and produce promotional materials, programs, and activities needed to support brand strategies in order to meet financial goals and expectations. This includes identifying and working effectively with external agencies, Brand Directors, Project Managers and consultants to meet expected project objectives and holding them accountable to agreed upon standards.
• Develop project and tactic assessments and valuations (ROI) that leverage analytics and research to identify successes. This includes working with market research and analytics to identify and implement metrics to gain market insights and measure performance on brand initiatives and programs.
• Participate in Medical, Legal, and Regulatory approval process for promotional programs.
• Monitor products, marketplace, and competitor trends and issues to anticipate/identify threats and opportunities. Make recommendations and develops tactics to respond to threats and opportunities.
• Maintain effective relationships and work with commercial partners to communicate and ensure alignment on strategy, messaging and execution within scope of projects.
  

Skills and Requirements

• Degree level or equivalent in Science and/or Business
• Desirable (but not essential) degrees: DipM, MBA or equivalent
• Demonstrated pharmaceutical industry experience to include expertise in marketing strategy and tactics and commercial policies and practices
• Demonstrable experience in developing strong collaborations with all stakeholders
• Global oncology commercial and strategic experience
• Experience working on cross-functional development teams especially in the context of the Oncology Business Group
• Strong project and process management skills, along with the ability to work on multiple tasks, and to effectively prioritise
• Demonstrated track record of marketing success, as demonstrated by successful product launches and/or sustained commercial growth; knowledge and experience of the Oncology market
• Advertising & Promotion - reviews core brand messages and sales strategy to be used in brand communication strategies and messaging.
• Field Force Dynamics - understands the dynamics of the Sales Force, Front Line Sales Managers and Medical Scientific Liaisons.
• Excellent team player.
• Appropriate level of diplomacy.
• Proactive self-starter.

To Apply

ProClinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies.

#LI_FH1

Industries:

Proclinical has partnered with a multinational pharmaceutical company in search for a Global Regulatory CMC Scientist to join the office in Slough. In this role you will be responsible for regulatory CMC for all NBE products in development. Provide support, or lead as assigned, regulatory CMC submissions for all products within the scope.

Job Responsibilities

• Support for developing and implementing the regional CMC regulatory strategy and submission plans for assigned projects/products to deliver timely approvals to meet business needs in regions assigned, and in line with the global regulatory strategy.
• Identifies supporting documents required for regional submissions and negotiates the delivery of approved technical source documents in accordance with project timelines.
• Responsible for writing regional and global CMC documentation for submissions as agreed with the Global Regulatory CMC Lead or (Global) Regulatory CMC Scientist if applicable, in line with agreed global regulatory strategy, and within agreed timelines.
• Highlights anticipated and ongoing critical issues arising through the product life-cycle in a timely manner to enable communication to key stakeholders (including TSO Practice Teams, GRA Practice Teams, PVU through the PVU GRL and the appropriate management level in the TSO Practice) as appropriate.
• Contribute to the preparation of the CMC SWOT analysis (or regulatory Risk Capture Document) and supports associated RA CMC challenge sessions.
• Leads or provides support to cross-functional teams responsible for the preparation of responses to HA CMC questions raised in regions assigned as delegated by the Global Regulatory CMC Lead (or Global Regulatory CMC Scientist, if applicable) for assigned projects/products.
• Monitors and reacts as appropriate to changes in the CMC regulatory environment in regions assigned for assigned projects/products to support and advice TSO Practice Teams and PVU.
• Establishes and maintains modes for effective communication and collaboration with the Global Regulatory CMC Lead (or Global Regulatory CMC Scientist if applicable), PVU GRL and GRA functions for assigned projects/products.
• Provides regulatory assessments for CMC changes and creation of entries and updates in the designated systems (Trackwise, UPILOT etc.) for assigned regions within defined timelines, as agreed with Global Regulatory CMC Lead (or Global Regulatory CMC Scientist if applicable).
• Provides regulatory affairs CMC input in TO Practice Teams as delegated by Global regulatory lead or scientist.
• Leads or provides input to internal regulatory business initiatives and cross functional work streams as assigned.

Skills and Requirements

• At least 5-8 years relevant experience in the pharmaceutical industry or a regulatory authority in a CMC review capacity, with at least 5 years of experience in Regulatory Affairs CMC and preferably 3 years professional experience in pharmaceutical manufacturing, analytical development, and quality assurance/control or related technical field
• Proven track record of successful authoring and contribution to delivering CMC sections of marketing authorisations for new biological and/or chemical entities
• Broad background of registration experience gained from working in the pharmaceutical industry or a regulatory authority in one of the ICH regions on development and post-approval products
• Experience of direct communication and negotiation with regulatory agencies on CMC matters
• Experience of participating in regulatory agency meetings on CMC matters
• Knowledge of GMP requirements and standard systems (e.g. change management systems and tools)
• Demonstrated competence in contributing on cross-functional teams and operating within a matrix organisational structure

To Apply

ProClinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies.

#LI_PD1

Industries:

Proclinical has partnered with a large pharmaceutical company in search for a Regulatory Affairs Consultant. You will be expected to provide expertise in the development, registration and post approval activities of medicines and ensuring high quality and timely delivery to our clients.

This is an excellent opportunity for a talented, independent and self-motivated regulatory professional to join a team that will not only provide you with a wide variety of experience in regulatory projects, it will also give you all the support you need to develop your regulatory career.

Job Responsibilities

• Exposure to a wide variety of regulatory projects providing strategic advice to optimise regulatory pathways for clients
• Supporting the preparation of regulatory documentation including ODD, PRIME, CTA, Ethics and MA applications
• Providing support to clients in technical dossier requirements and compiling modules of the CTD for various product developments
• Forging strong relationships with clients and regulatory agencies through scientific advice meetings and agency negotiations
• Being part of a small, high performing team, you will be involved in mentoring other team members on key projects
• The opportunity to play a part in growing and enhancing the strong reputation the company already has in the regulatory industry.

Skills and Requirements

• Life Sciences Graduate or Pharmacist, ideally with a post-graduate qualification
• At least 5 - 7 years' experience in the medicines industry
• Experience in writing EU regulatory documents with sound knowledge of the EU medicines Directive associated guidelines
• Proven capability in working on multiple projects and effectively managing time to meeting critical timelines
• Able to demonstrate effective communication skills in dealing with diverse group of stakeholders
• A willingness to support resolving complex issues and driven to deliver results
• Good organisational and analytical skills with the flexibility to work across multiple client projects, with excellent attention to detail
• You will be expected to work independently on a day-to-day basis, whilst integrating into team project work.
• The successful candidate will also be fluent in written and spoken English

To Apply

ProClinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies.

#LI_PD1

Industries:

Proclinical have partnered with this exciting medium-sized, fully integrated Pharmaceutical company that develop and manufacture their own products in Oncology, Neurology and CNS. They have an excellent culture and have one of the most exciting pipelines in the industry.

Role Overview:

Reporting into the Director of Clinical Quality Assurance you will be responsible for Quality oversight activities for this company's clinical trials, systems and vendors. You will be leading audits as well as taking full responsibility for hosting and managing the Health Authority Inspection strategy ensuring inspection readiness at all times. This role is truly cross-functional involving management of internal and external stakeholders and leading Quality Improvement initiatives across the company. High-visibility role with huge impact across the business with a chance to worked autonomously as well as collaboratively.

Required Skills Experience:

You will need to be educated to at least Bachelor's degree level and have demonstrable experience in a Clinical Quality Assurance setting within a Pharmaceutical or Biotech environment. You will have thorough knowledge of Clinical Operations and fundamental knowledge of the US, EU and international regulatory standards that they must adhere to. You will have extensive experience of planning and carrying out routine, complex and for-cause GCP audits as well as ideally having Inspection Management/Readiness experience..

In return they are offering a highly-competitive salary and benefits package as well as an environment that will uniquely challenge you with the infrastructure to develop you professionally.

This will be office-based in Hatfield but with flexibility to work from home if neccessary.

To Apply

ProClinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies.

#LI_JG1

Industries:

A large multinational organisation is in search for The Head of Customer Excellence & Operations (CE&O) leader. You will report to the Managing Director and have an impact across therapeutic areas and functions focusing on ways to optimise engagement with its customers.

Job Responsibilities

• Leadership to MCE function - Build on existing foundations to accelerate digital component of new Go-to-market models including omnichannel campaign approach, content plans, channel buildouts and optimization, metrics setting and tracking and customer feedback.
• Field Force Effectiveness (FFE)
• Leadership to FFE activities including but not limited to CRM capabilities, FF sizing, structuring, targeting, segmentation, Incentive Compensation planning, Performance Analytics, Strategic Account Planning (and SAM/KAM) and dashboards.
• Customer and Market Insights (CMI) and Data & Analytics (D & A)
• Leadership to CMI function, leveraging primary and secondary data, market research, competitive intelligence, forecasting & analytics (patient/market) and performance narrative, to provide insights and analytics to support local brand teams and affiliate leadership with critical decision making and strategy. Translates data/insights into short/mid-term forecasting of business performance/expectations. Build & optimize data and analytics capabilities (data visualization, automation, Artificial Intelligence etc.)
• Capabilities & Training
• Establish new function and then drive implementation through support for new Head of Capabilities & Training. Undertake gap analysis to identify needs across all BU's/functions, build 1-3 year Roadmap and then drive implementation.
• Overall Customer Excellence
• Enhance customer engagement capabilities/frameworks leveraging superior customer insights. Actively participate in sharing/executing best practices. Drive local aspect of Global customer initiatives to advance to the preferred partner for patients, prescribers and payers through innovative services/solutions. Lead definition, optimization and evolution of Customer Engagement Strategy (products, segment, and channels) and related operations driving greater efficiency and effectiveness.

Skills and Requirements

• Strong pharmaceutical or biotechnology industry experience and driving customer excellence type of functions
• Proven track record in leading Customer Excellence teams at local level.
• Advanced analytical & strategic skills.
• A deep understanding of FFE and operating model design / transformation.
• In depth experience of customer excellence related activities and processes and ideally of multichannel excellence.
• Participation/leadership in defining and implementing affiliate strategy
• Credible, dynamic and creative professional with the energy and vision to lead a successful organization.
• Thrive on challenge and will be highly collaborative, perceptive, an analytical problem solver, and exhibit strategic and innovative agility.
• Someone who manifests trust, and is known for ethics and integrity, and works successfully in a team environment.
• Excellent communication skills and a strong personal presence.
• Proven track record of driving change management internally
• Proven record of leading and developing people
• Proven track record in a highly competitive marketplace
• Fluent in English and local language
• BA/BS Required. MBA a plus

To Apply

ProClinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies.

#LI_HW1

Industries:

Trainee Recruitment Consultant- German Speakers (Entry Level or Experienced Recruiter Life Sciences preferred but not essential)

Location: London (2 minute walk from London Liverpool Street Station or a 3 minute walk from Moorgate Station)

Salary: £23,000+ Basic (Negotiable dependent on experience + Uncapped & luxurious incentives including holidays, directors lunch and much more!)

Start Date: As soon as you're available!

We Offer You:

• Quick Career Progression - At least one promotion a year with multiple tailored career paths including 360 Perm and/or Contract, Client Services, MSP, Delivery based teams, Executive search, Leadership and International Opportunities amongst others. Across the business we have a lot of roles to work on so there isn't as much a need to do BD like there is in most recruitment companies.
• High Earning Potential and Uncapped Commission - Average OTE £27-30K+ YR1, £40-55K+ YR2, £60K - £70K+ YR3 and a salary increase with each promotion
• 9 - 6 working hours and an earlier finish on Friday with dress down
• Not KPI driven, realistic targets you can achieve as we believe in a positive environment
• Promote international moves - Los Angeles, New York, San Francisco, Philadelphia, Boston, Basel, Stockholm, Frankfurt, Switzerland, Singapore, Sydney, Melbourne, Beijing, Tokyo, Shanghai and more offices to start up within the next 2 years
• Access to a large international client base
• Annual incentive trips away to Cape Town, Cancun, Singapore, Vegas, New York, Skiing etc.
• Multiple Services to offer clients which makes you more appealing when winning business
• Incentives include trips to the theatre, horse racing, go karting and Michelin star restaurants.
• Continuous Support and Training with both your mentor and our Learning and Development team regardless of your level
• Dynamic and Inclusive Culture
• Fun Office space located by London Liverpool Street
• Company Benefits - Pru Vitality healthcare, Subsidised Virgin Active gym membership, Extended gym lunches, Season ticket travel loan, Contributory pension scheme, Childcare vouchers, Cycle to work scheme
• Hire into roles/projects that have a moral purpose

Your Role and Responsibilities:

With the initial job title of Associate Consultant, you will be fully trained in all aspects of recruitment by one of the senior members of the company and our Learning and Development team. During your time in this role, you will be working with a Senior / Principal Consultant and tasked with finding suitable candidates for open job vacancies across Europe.

Responsibilities include:

• Advertising jobs on social media sites
• Searching for resumes via the database
• Head-hunting candidates and networking on social media platforms
• Taking referrals and adding CVs to the database
• Introducing yourself to and briefing candidates about job opportunities
• Discussing financial packages, timing and travel etc

Working against many competing firms and their candidates, you will have some successes and some disappointments. You will be rewarded with commission for every placement that you make during your time as a Resourcer and if successful then you can be rewarded with a promotion and will be introduced to client management and business development (Consultant).

What you need to have:

• Fluent in German
• Must be a Professional or Fluent level in English
• Life Science Recruitment experience or in another industry is not essential but would be a plus
• A Motivated attitude
• Drive and ambition
• A strong work ethic
• An entrepreneurial spirit
• Strong business acumen
• Resilience
• Scientific knowledge and sales experience is preferable; however it is not essential
• Eager to learn

Company:

As Global Growth Partners, we provide a unique proposition: delivering on

every stage of the life science process to help individuals, teams, and whole

organisations reach their goals faster. Through our suite of solutions - Proclinical

Staffing, Proclinical Executive, Proclinical Consulting and Proclinical Engage

- we help them to grow so that they can bring about a positive impact on global

health.

And, just as we help our life science partners with their businesses and careers,

we cultivate an environment for personal and career growth within our own

company too. Our values: Long-term partners; Tireless experts; and Promises

delivered; form the basis of what we look for in new team members. These values

are engrained in every part of our business, from how we run our learning and

development programmes to how we define criteria for reward and recognition.

Industries:

Job Title: IT Service Desk Engineer

Division/Dept/Location: UKICSG - IT - London Liverpool Street/Moorgate Station area

Company: Proclinical apart of ICS

Responsible to: IT Service Desk Team Leader

Salary: £25k+ dependent on experience

Job Scope:

The candidate will need excellent customer service skills coupled with a strong technical computer background. Ability to take responsibility for IT incidents, requests, problems and proactively seek resolutions for customers; keep customers informed of progress; deal with problems and complaints in a professional, calm manner. Support both internal and external customers. Key skills include ITIL, MS Office365, MS operating systems, computer hardware, printers, phone systems, good working knowledge of network topologies and excellent customer services skills.

Key Tasks:

• Provide the customer interface to the IT Service Desk via face-to-face, telephone and electronic communications.
• Logging of Service Desk calls, ensuring all the fields are completed, assigning the correct priority status to the call.
• Working to ITIL best practices.
• Take responsibility for faults and work requests. Proactively seek resolutions for customers; keep customers informed of progress; deal with problems and complaints in a professional, calm manner.
• Provide technical support on all IT related matters aiming at resolving majority of incidents at first point of call using advanced diagnostic techniques, system administrator rights and remote control of desktops.
• Ensure the company IT audit system is kept updated when hardware and software changes are made.
• User account creation for domain, email and application accounts.
• Support the company front and back office applications.
• Keep abreast of current and emerging hardware and software technologies.
• Maintain a personal development programme as agreed with line manager.
• Any other reasonably IT related duties required.
• Travel to branch offices within the UK to provide support when required.
• May be expected to work hours between 8am to 6pm when required to cover oncall periods. Note that these oncall start and end times may change.

Education / Qualifications / Knowledge

• Good level of basic education - Essential
• Degree - Desirable

Skills / Training

• Multiple MCP - Desirable
• ITIL - Desirable
• Fuze Telephony - Desirable
• VMware - Desirable
• Thin Client - Desirable
• Terminal Server - Desirable

Experience

• MS Office365 Experience - Essential
• MS Client Operating System experience - Essential
• Experience in a similar job role - Essential
• Microsoft teams - Desirable
• Bullhorn - Desirable
• Service Now - Desirable
• MS Operating System experience Win 2016/2019 Server - Desirable
• Hardware experience computer, monitor, scanner, printer - Desirable
• Microsoft knowledge - Desirable
• User account creation for domain, email and application account -Desirable

Disposition / Personal / Qualities

• Support and encourage the company culture.
• Ability to work in a team
• Self motivated
• Self reliant
• Excellent communicator

Company:

As Global Growth Partners, we provide a unique proposition: delivering on

every stage of the life science process to help individuals, teams, and whole

organisations reach their goals faster. Through our suite of solutions - Proclinical

Staffing, Proclinical Executive, Proclinical Consulting and Proclinical Engage

- we help them to grow so that they can bring about a positive impact on global

health.

And, just as we help our life science partners with their businesses and careers,

we cultivate an environment for personal and career growth within our own

company too. Our values: Long-term partners; Tireless experts; and Promises

delivered; form the basis of what we look for in new team members. These values

are engrained in every part of our business, from how we run our learning and

development programmes to how we define criteria for reward and recognition.

To Apply

ProClinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies.

#LI_SR1

Industries:

Skills:

An exciting opportunity has arisen for a talented and experience Senior Clinical Research Assocaite to join a large company. The role is accountable for performance and compliance for assigned protocols and sites in a country, you will ensure compliance of study conduct with ICH/GCP and country regulations. You will be given the opportuntiy to focus on your clinical career growthv acting as primary site manager throughout all phases of a clinical research study and taking responsibitly of allocated sites.

We are a research-driven biopharmaceutical company. Our mission is built on the simple premise that if we "follow the science" and that great medicines can make a significant impact to our world. And we believe that a research-driven enterprise dedicated to world-class science can succeed by inventing medicine and vaccine innovations that make a difference for patients across the globe.

You will be expected to:

• Exhibit effective time management, organizational and interpersonal skills, conflict management, problem solving skills
• Able to work highly independently across multiple protocols, sites and therapy areas.
• High sense of accountability / urgency. Ability to set priorities and handle multiple tasks simultaneously in a changing environment.
• Works effectively in a matrix multicultural environment. Ability to establish and maintain culturally sensitive working relationships.
• Demonstrates commitment to Customer focus.
• Works with high quality and compliance mind-set

Skills and Requirements

• Required: Min. 2 years of direct site management (monitoring) experience in a bio/pharma/CRO for Oncology protocols.
• Educational Requirements
• Preferred: B.A./B.S. with strong emphasis in science and/or biology

To Apply

ProClinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies.

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