Freelance Clinical Trial Manager

I-Pharm Consulting are partnering with a global biopharmaceutical company who are looking for a Clinical Trial Manager who will be responsible for the management of post-authorisation studies and Investigator Sponsored Research across different therapeutic areas.

THE COMPANY

Leading Biotech with a global presence in over 100 countries. i-Pharm has been a dedicated recruiter for this client for several years and have had great feedback on the company's career progression, culture and job satisfaction from candidates placed in both permanent and contract positions.

and Investigator Sponsored Research across different therapeutic areas.

TITLE:

Clinical Trial Manager

The Role:

You will be involved in:

• Operational management of post-authorisation studies and investigator led studies.
• Manages CROs/vendors for assigned post-authorisation studies.
• Feasibility assessment
• Contributes to development and maintenance of study budgets.
• Ensuring project team goals are met.
• Conduct study feasibility in conjunction with internal Medical Affairs and Clinical Operations staff and/or external collaborators or CROs.
• Contributes to Clinical Operations International team activities & initiatives.

EXPERIENCE

• Experience managing Phase IV and Non-Interventional studies
• Must be able to prioritize multiple tasks.
• Good knowledge and understanding of ICH GCP, GVP, FDA and EMEA regulations and guidelines applicable to post-authorization studies.
• Knowledge of different types of post-authorisation safety and efficacy studies
• Experience in the review and oversight of Investigator Lead trials sought after.
• Excellent teamwork, communication, decision-making and organizational skills

LOCATION:

West London

DURATION:

12 Month Contract - Freelance

RATE:

Competitive Daily Rate

ABOUT I-PHARM CONSULTING:

i-Pharm Consulting is a specialist Recruitment Company servicing the Pharmaceutical industry in the UK and Europe. We provide both permanent and contract staff to a wide range of Pharmaceutical, Medical Device, Biotechnology and Contract Research Organisations (CROs). i-Pharm has specific expertise in Clinical Research, Medical Affairs, Regulatory Affairs, Pharmacovigilance, Quality Assurance and Bioinformatics.

TO APPLY:

If you would like to discuss this vacancy further, please call Zara Linehan on +44(0)2031890470, or zlinehan@i-pharmconsulting.com. If this role is not suitable, Zara is also available to discuss other possible positions or answer any general questions regarding your career and the current market.

KEYWORDS:

CTM / Clinical Trial Manager / Trial Management / Study Manager / Project Manager / Study Management / Biotech / Biotechnology / Biopharma / Biopharmaceutical / Pharmaceutical / CRO / Clinical Research Organisation / Inflammation / Bowel Disease / Rheumatism / Rheumatology / HIV / Infectious Diseases / Phase IV / Late Phase / Post Marketing / Investigator / Non-Interventional / London / West London / Uxbridge / Hayes / Buckinghamshire / Maidenhead / High Wycombe / Marlow / Slough / Reading