Clinical Study Manager

19 Nov 2018
19 Dec 2018
NTCA - Studymanager
Contract Type

I have recently partnered with a client based in the north of England who are looking for a Clinical Study Manager to join their team for 3 - 6 months on a freelance basis. This is a fantastic opportunity for someone who is looking to broaden their portfolio with a niche Pharma company.

The contract is for 1 FTE and will be working in their office directly with the Director of Clinical Operations and the clinical team as a whole.

Main Responsibilities:

Attend site visits with CRO personal to develop relationships with investigators and review processes

International study management of the growing number of studies currently outsourced to CRO's

Aid with effective coaching and development of more junior members of the team

Development of a monitoring program to ensure sponsor oversight compliance

Collaboratively work with key cross functional teams across the clients structure

Required Experience/Qualifications:

On-site monitoring experience within the last two years

Keen understanding of core teams within the clinical setting such as regulatory, data management and medical writing

Recently worked with a Pharma or Biotech

Detailed knowledge of ICH/GCP, recent updates and adaptive monitoring approaches

Previously been involved with investigator meetings

Degree in a health or scientific discipline or relevant experience of 10 or more years

At least 5 years experience with CRA activities (feasibility /site set up, direct site monitoring, eCRF process etc.)

You will also be required to have a full UK driver's license and ability to travel across the UK as/when required.


If this role sounds like something you are interested in then get in touch ASAP as to avoid missing out. Feel free to also send the contact details of anyone you know that could be ideal for this position.

+44 1293 77 66 44

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