Clinical Study-Start up Specialist - Reading/ Slough - Up to £40K

Recruiter
Meet Recruitment Ltd
Location
London (Greater)
Salary
Circa £45,000
Posted
13 Nov 2017
Closes
15 Nov 2017
Sector
Healthcare
Contract Type
Permanent
Hours
Full Time
Clinical Study-Start up Specialist, Study Start-up - Reading/Slough - Up to £40K

We are currently recruiting for a highly recognised CRO that are growing their study start-up team as a core function. This is a great time to join this team as it is set to grow and develop rapidly in the future.

This position is being dealt with by Zoe Benningfield-Fox @Meet

Responsibilities:

- Accountability for delivery to time, cost and quality for assigned activities
- Primary contact with investigative sites during site start-up activities
- Responsible for working with investigative sites to collect the required investigator and regulatory documents
- Responsible for maintenance of regulatory documents

This position is being dealt with by Zoe Benningfield-Fox @Meet

Requirements:

- Life Science degree
- Excellent communication, organisational and time management skills
- Works well in a team as well as independently
- Detail and process orientated
- Positive attitude and approach

This position is being dealt with by Zoe Benningfield-Fox @Meet

Meet is a European wide recruitment agency who specialise purely in the pharmaceutical sector. We work in a number of regions across Europe placing both permanent and freelance candidates into Clinical, Regulatory and Data management teams within CRO's, Pharmaceutical, Generic and Biotech companies.

If you are interested in finding a new opportunity however the one shown in this advert is not suitable for you please do not hesitate to contact us! Our number is ************* or visit our website - *************************** to upload your CV.

Clinical Research associate, CRA, In-house CRA, CTA, Clinical Trials Associate, CTC - Clinical trial Coordinator, Regulatory, Regulatory submissions, MHRA, Ethics submission, Start-up, Study Start up, Site manager, Site specialist, feasibility, regulatory affairs, EC submissions, Clinical Research associate, CRA, In-house CRA, CTA, Clinical Trials Associate, CTC - Clinical trial Coordinator, Coordinator, Regulatory, Regulatory submissions, Site manager, Site specialist, feasibility, regulatory affairs, EC submissions,