Clinical Trial Manager - Global Pharma - Complex Trials
Posted a month ago
- London, Greater London
- Any
- External
- Expires In 2 months
Title: Clinical Trial Manager - Global Pharma - Complex Trials
Location: London
Duration: Full Time
Salary: Competitive Based on Experience
We’re very excited to be partnering with a Global Pharma who are seeking a Clinical Trial Manager, due to a expanding pipeline within Virology development. You will be apart of significant growth within its pipeline in Virology through internal research, partnerships and acquisitions.
The Role:
Provides regional management of global PIb-III studies managed by Clinical Program Manager
Drafts and coordinates review of relevant documents including protocols, informed consents, case report forms, monitoring plans, investigator brochures, and clinical study reports
Maintains study timelines
Contributes to development of study budget
Contributes to development of RFPs and participates in selection of CROs/vendors.
Desired Skills and Experience:
Significant relevant experience and a BSc or nursing qualification in a relevant scientific discipline
Previous experience in Virology areas would be advantageous but not essential
Must have previous study management/coordination experience at Sr CTMA level
Monitoring experience is highly desirable as co-monitoring will be required
Thorough knowledge and understanding of FDA and EU Regulations, ICH Guidelines, and GCPs governing the conduct of clinical trials is desirable
If you would like to discuss this vacancy further or to discuss your career options in confidence, please telephone on +44 (0) 2039288383 or email me on: #####
If this role isn’t suitable for you, please let us know if you can refer anyone – any recommendations are much appreciated! Planet Pharma offers a competitive referral scheme so you will be rewarded for your help!
About Planet Pharma
Planet Pharma is an American parented Employment Business/Agency that provides global staffing services with its head-quarters in Chicago and our EMEA regional office located in Central London. We have invested significantly in creating a robust international platform that enables us to work compliantly in 30+ countries with a current network of 2500+ active contractors globally as well as a very strong permanent / direct hire recruitment offering.
Our specialist knowledge and close relationships with our clients and the wider industry really makes us unique in our field. Just recently we were recognised by FORBES as the 17th best professional staffing firm, and have won multiple awards from industry accredited bodies for our commitment to excellence and service delivery. We have extensive functional expertise including: Regulatory Affairs, Pharmacovigilance, QA, QC, Submissions experts, Clinical development, Quality, Biostatistics, and Medical Affairs / Writing.
We are an equal opportunities Recruitment Business and Agency.
We welcome applications from all suitably qualified candidates regardless of their race, sex, disability, religion/belief, sexual orientation or age.
www.planet-pharma.com
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Location: London
Duration: Full Time
Salary: Competitive Based on Experience
We’re very excited to be partnering with a Global Pharma who are seeking a Clinical Trial Manager, due to a expanding pipeline within Virology development. You will be apart of significant growth within its pipeline in Virology through internal research, partnerships and acquisitions.
The Role:
Provides regional management of global PIb-III studies managed by Clinical Program Manager
Drafts and coordinates review of relevant documents including protocols, informed consents, case report forms, monitoring plans, investigator brochures, and clinical study reports
Maintains study timelines
Contributes to development of study budget
Contributes to development of RFPs and participates in selection of CROs/vendors.
Desired Skills and Experience:
Significant relevant experience and a BSc or nursing qualification in a relevant scientific discipline
Previous experience in Virology areas would be advantageous but not essential
Must have previous study management/coordination experience at Sr CTMA level
Monitoring experience is highly desirable as co-monitoring will be required
Thorough knowledge and understanding of FDA and EU Regulations, ICH Guidelines, and GCPs governing the conduct of clinical trials is desirable
If you would like to discuss this vacancy further or to discuss your career options in confidence, please telephone on +44 (0) 2039288383 or email me on: #####
If this role isn’t suitable for you, please let us know if you can refer anyone – any recommendations are much appreciated! Planet Pharma offers a competitive referral scheme so you will be rewarded for your help!
About Planet Pharma
Planet Pharma is an American parented Employment Business/Agency that provides global staffing services with its head-quarters in Chicago and our EMEA regional office located in Central London. We have invested significantly in creating a robust international platform that enables us to work compliantly in 30+ countries with a current network of 2500+ active contractors globally as well as a very strong permanent / direct hire recruitment offering.
Our specialist knowledge and close relationships with our clients and the wider industry really makes us unique in our field. Just recently we were recognised by FORBES as the 17th best professional staffing firm, and have won multiple awards from industry accredited bodies for our commitment to excellence and service delivery. We have extensive functional expertise including: Regulatory Affairs, Pharmacovigilance, QA, QC, Submissions experts, Clinical development, Quality, Biostatistics, and Medical Affairs / Writing.
We are an equal opportunities Recruitment Business and Agency.
We welcome applications from all suitably qualified candidates regardless of their race, sex, disability, religion/belief, sexual orientation or age.
www.planet-pharma.com
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