Role Summary:
- The primary role of the Project Leader is to lead and manage domestic or international projects.
- May be part of a global project management team.
- Requires some interaction/supervision by Line Manager or Senior Project Leader or Director.
- Project Leaders may mentor junior staff and Functional Leads for specific projects.
- Project Leaders participate in proposal development teams, giving input to particular indication and operational structure for th

Calyso Analyst Developer

Senior Late Phase Research Associate - UK office based

If you are looking to further your CRA career within a International organisation.

FREELANCE/CONTRACT/ CRA - CLINICAL RESEARCH ASSOCIATE,
Homebased, UK

CRA/Clinical Research Associate
6 Month Contract - Based in Netherlands - Start ASAP - 4 Days a week

My client is a big international and dynamic pharmaceutical company

You have at least 1 year relevant experience as a CRA.

Investigator Contracts Associate / Senior CRA

Roles are available in Spain and Romania

You will support the Investigator Contracts Group by reviewing and negotiating Investigator Contracts and related documents, ensuring timely completion and submission to Investigators and Sponsors.

Proposal Development Associate ( 12 Month Assigment)

Working within a highly qualified team you will be responsible for supporting business Development in the winning of new business for my client You will organize and prepare high quality customer-focused proposals and budgets for the conduct of clinical trials.

Our world leading international pharmaceutical company, we are seeking for 2 Regulatory CMC Specialists / Product Specialists for the department of Network CMC (Chemistry Manufacturing & Control in the Netherlands.

SENIOR CRA/CLINICAL RESEARCH ASSOCIATE - GERMANY -
FIELD BASED/HOMEBASED

My client is looking for a home based Senior Clinical Research Associate/CRA to perform routine site visits to ensure that the rights and well, being of human subjects are protected; to make sure that the reported trial data are accurate, complete, and verifiable from source documents; and that the conduct of the trial is in accordance with the currently approved protocol/amendment(s), SOPs, GCP/ICH Guideline

CLINICAL TRIAL SPECIALIST - BELIGUM

Clinical Trial Specialist needed for office based role in Belgium working for a Top 5 Global client who are rapdily growing and developing, then this is the position for you: