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Job Details

Clinical Team Lead (CTL) / Prague, Czech Republic

Company: Covance
Location: Prague, Czech Republic
Reference: 2017-15157
Closing Date: 30 Nov 17
Type: Permanent
Salary (£): Competitive

Job Summary:

COVANCE is a leading global drug development services company and we provide support to the Pharmaceutical and Biotechnology industries. Are you ready for the next step in your career?


We are currently recruiting for a Clinical Team Lead ready to join our constantly growing CoSource team. This is a full-time, permanent and office-based position at our Client’s office in Prague.

As a Clinical Team Lead you will act as a member of the Core Project Team and will have overall responsibility and accountability for the execution of the clinical operations strategy of the project. Clinical Team Lead is responsible for coordinating and managing the clinical operations team, providing operational leadership and expertise to ensure successful execution of the clinical operations project deliverables (quality, timeline, budget and scope).

This role involves regular and proactive communication with the Sponsor, the Project Manager/Project Director and other functional groups, as appropriate. The successful candidate will serve as the main site monitoring and site management contact and support for the Project Manager and the client.

Education / Qualifications

- University/college degree (life science preferred), or certification in a related allied health profession (i.e. nursing, medical or laboratory technology) from an appropriately accredited institution;

- In lieu of the above requirement, candidates with six five or more years of relevant clinical research experience in pharmaceutical, CRO industries or experience in a health care setting will be considered;

- Thorough knowledge of ICH Guidelines and GCP including a basic understanding of regulatory requirements in other countries;

- Thorough understanding of the drug development process.


- Six years of relevant clinical research experience with an ability to demonstrate comprehensive understanding of ICH/GCP guidelines;

- Serious Adverse Event (SAE) reporting, process production of reports, narratives and follow up of SAEs;

- Site monitoring and study site management requirements;

- Applicable regional regulatory requirements;

- Experience in Diabetes Mellitus or Allergology preferred.

- Trip report review, risk planning, study plan development, resource planning and data management oversight.

- In lieu of the above requirements, candidates with two years of supervisory experience in a health care setting and four years clinical research experience (including monitoring) in the pharmaceutical or CRO industries will be considered.


Apply for this job: Clinical Team Lead (CTL) / Prague, Czech Republic

Contact Information:

Address:  Covance- Warsaw

Website:  Visit Our Web Site

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