Paramount Recruitment has extensive experience of recruiting within the Clinical Research market. We are preferred suppliers to many companies ranging from small independent Clinical Research Organisations to global Pharmaceutical and Medical Device companies.
Our Consultants understand the infinitely diverse range of opportunities within this field – from entry level CTA to Clinical Director, each role requires not only a unique set of skills but also a good understanding of specific therapeutic areas too.
If you are looking for a Clinical Research job, or your organisation needs to recruit, Paramount can assist with the following skill sets:
For more information regarding our Clinical Research jobs, or if you are looking to recruit staff into these types of roles, please contact our specialist Consultant:-
Clinical Research - Marie Tucker +44 (0) 121 616 3460 or
marie.tucker@paramountrecruitment.co.uk
Biometrics, SAS, Statistics - Jade Page +44 (0) 121 616 3472 or jade.page@paramountrecruitment.co.uk
Contract Clinical Trial Lead
Contract Clinical Trial Lead – Clinical Trials - Oncology – Pharmaceutical – Contract – Basel – Switzerland
An experienced contract Clinical Trial Lead is required to join one of the world’s leading pharmaceutical company based in Basel for a rolling 6 month contract. This role would suit an individual who enjoys variety in their day to day responsibility working with minimum supervision.
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Contract Clinical Trial Lead
Contract Clinical Trial Lead – Clinical Trials - Oncology – Pharmaceutical – Contract – Basel – Switzerland
An experienced contract Clinical Trial Lead is required to join one of the world’s leading pharmaceutical company based in Basel for a rolling 6 month contract. This role would suit an individual who enjoys variety in their day to day responsibility working with minimum supervision.
ApplyView Detail
| Salary: |
£200 Per Day |
| Location: |
South West England, England N/A |
| Category: |
Clinical Research |
Key Responsibilities:
The successful Clinical Trial Assitant (CTA) will be responsible for performing study site management activities. This includes Start up activities, regulatory compliance, patient enrolment, CRF compliance and data quality for Clinical Trials as well as developing and maintaining investigator relationships.
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