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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
ProClinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies.
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.
Skills and Requirements
To Apply ProClinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies.
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.
Skills and Requirements
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.
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.
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.
Skills and Requirements
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.
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.
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
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.
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.
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.
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:
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.
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:
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
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.
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
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.
Education / Qualifications / Knowledge
Skills / Training
Disposition / Personal / Qualities
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:
Clinical Research Jobs
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