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Clinical Trial Associate Position
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Slough, Slough, United Kingdom CK Group Full timeClinical Trial Associate Role:We are seeking a skilled Clinical Trial Associate to join our team at CK Group. As a Clinical Trial Associate, you will be responsible for developing a Trial Master File (TMF) Plan, conducting ongoing and final Quality Control (QC) checks of TMF, and supporting audit/inspection activities.Key Responsibilities:Develop a Trial...
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Slough, Slough, United Kingdom CK Group Full timeClinical Trial Associate Job DescriptionCK Group is recruiting for a Clinical Trial Associate to join a global pharmaceutical company on a contract basis initially for 12 months. The successful candidate will be based in Slough.Key Responsibilities:Develop a Trial Master File (TMF) Plan and conduct ongoing and final Quality Control (QC) checks of TMF.Support...
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Slough, Slough, United Kingdom CK Group Full timeClinical Trial Associate Position OverviewWe are seeking a highly skilled Clinical Trial Associate to join our client's global pharmaceutical company in Slough, UK. As a Clinical Trial Associate, you will be responsible for developing and maintaining Trial Master Files (TMFs), conducting quality control checks, and supporting audit and inspection...
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Clinical Research Associate
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Clinical Research Associate
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Clinical Trial Associate
2 months ago
Job Summary:
Clinical Trial Associate - Contract
About CK Group:
CK Group is a leading provider of scientific, clinical, and technical services to the pharmaceutical and biotechnology industries.
Job Description:
We are seeking a highly skilled Clinical Trial Associate to join our team on a contract basis. As a Clinical Trial Associate, you will be responsible for:
- Developing and maintaining Trial Master Files (TMFs) to ensure compliance with regulatory requirements.
- Supporting audit and inspection activities to ensure the quality and integrity of clinical trials.
- Participating in clinical study team meetings to provide expertise and support.
Requirements:
- Relevant scientific degree or equivalent working experience.
- Previous experience with creating Trial Master Files within the pharmaceutical industry.
About the Company:
Our client is a global biopharmaceutical company focused on creating value for people living with severe diseases in immunology and neurology.
What We Offer:
- Opportunity to work with a leading pharmaceutical company.
- Chance to develop your skills and expertise in clinical trials.
- Collaborative and dynamic work environment.