Clinical Trials Coordinator

4 weeks ago


Slough, Slough, United Kingdom CK Group Full time
Position Overview:

CK Group is seeking a Clinical Trial Associate to support a leading global pharmaceutical organization on a contract basis.

Compensation:

Hourly rate: £20.03 PAYE or £27.27 via Umbrella.

Key Responsibilities:
  • Establish and maintain a comprehensive Trial Master File (TMF) Plan, ensuring ongoing and final Quality Control (QC) assessments of the TMF.
  • Assist in audit and inspection preparations while collaborating with the Clinical Development Quality Lead (CDQL).
  • Serve as a subject matter expert on client systems, continuously seeking efficiencies between client and partner systems.
  • Engage in Clinical Study Team meetings and other trial-related discussions when specialized knowledge is required.
Candidate Profile:
  • Possess a relevant scientific degree or equivalent professional experience.
  • Demonstrated experience in creating Trial Master Files within the pharmaceutical sector.
  • Exceptional communication skills.
  • Strong attention to detail.
Company Overview:

Our client is a prominent biopharmaceutical company dedicated to enhancing the lives of individuals affected by severe diseases in the fields of immunology and neurology.

Important Note:

Applicants must have the right to work in the UK. This position may require a satisfactory basic Disclosure and Barring Service (DBS) check.

  • Slough, Slough, United Kingdom CK Group- Science, Clinical and Technical Full time

    Job Summary:Clinical Trial Associate - ContractAbout 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...


  • Slough, Slough, United Kingdom CK Group- Science, Clinical and Technical Full time

    Job Summary:Clinical Trial Associate - ContractAbout 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...


  • Slough, Slough, United Kingdom CK Group- Science, Clinical and Technical Full time

    Job Summary:Clinical Trial Associate - ContractAbout 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...


  • Slough, Slough, United Kingdom CK Group- Science, Clinical and Technical Full time

    Job Summary:Clinical Trial Associate - ContractAbout 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...


  • Slough, Slough, United Kingdom CK Group Full time

    Job DescriptionCK Group is seeking a highly skilled Clinical Trial Associate to join our team on a contract basis. This role is an excellent opportunity for a motivated individual to work with a global pharmaceutical company based in Slough.Key Responsibilities:Develop and Maintain Trial Master Files (TMFs): Create and implement TMF plans, conduct ongoing...


  • Slough, Slough, United Kingdom CK Group Full time

    Job DescriptionCK Group is seeking a highly skilled Clinical Trial Associate to join our team on a contract basis. This role is an excellent opportunity for a motivated individual to work with a global pharmaceutical company based in Slough.Key Responsibilities:Develop and Maintain Trial Master Files (TMFs): Create and implement TMF plans, conduct ongoing...


  • Slough, Slough, United Kingdom EPM Scientific Full time

    About EPM ScientificWe are a pioneering pharmaceutical company dedicated to the discovery, development, and delivery of innovative treatments for patients with rare and life-threatening diseases. Our mission is to transform the lives of those affected by these challenging conditions through cutting-edge research and patient-centric drug development.Job...


  • Slough, Slough, United Kingdom CK Group Full time

    Job DescriptionCK Group is seeking a highly skilled Clinical Trial Associate to join our team on a contract basis. This role will be based at our client's site in Slough.Key Responsibilities:Develop and Maintain Trial Master Files: Create a Trial Master File (TMF) Plan and conduct ongoing and final Quality Control (QC) checks of TMF.Support Audit and...


  • Slough, Slough, United Kingdom CK Group Full time

    Job DescriptionCK Group is seeking a highly skilled Clinical Trial Associate to join our team on a contract basis. This role will be based at our client's site in Slough.Key Responsibilities:Develop and Maintain Trial Master Files: Create a Trial Master File (TMF) Plan and conduct ongoing and final Quality Control (QC) checks of TMF.Support Audit and...


  • Slough, Slough, United Kingdom EPM Scientific Full time

    About EPM ScientificWe are a pioneering pharmaceutical company dedicated to the discovery, development, and delivery of innovative treatments for patients with rare and life-threatening diseases. Our mission is to transform the lives of those affected by these challenging conditions through cutting-edge research and patient-centric drug development.Key...


  • Slough, Slough, United Kingdom EPM Scientific Full time

    About EPM ScientificWe are a pioneering pharmaceutical company dedicated to the discovery, development, and delivery of innovative treatments for patients with rare and life-threatening diseases. Our mission is to transform the lives of those affected by these challenging conditions through cutting-edge research and patient-centric drug development.Job...


  • Slough, Slough, United Kingdom EPM Scientific Full time

    About EPM ScientificWe are a pioneering pharmaceutical company dedicated to the discovery, development, and delivery of innovative treatments for patients with rare and life-threatening diseases. Our mission is to transform the lives of those affected by these challenging conditions through cutting-edge research and patient-centric drug development.Job...


  • Slough, Slough, United Kingdom EPM Scientific Full time

    Job DescriptionJob Title: Clinical Trial Regulatory LeadCompany: EPM ScientificJob Type: Full-timeLocation: RemoteJob Category: PharmaceuticalAbout Us:EPM Scientific is a leading provider of scientific and regulatory services to the pharmaceutical and biotechnology industries. We are committed to delivering high-quality solutions that meet the evolving needs...


  • Slough, Slough, United Kingdom EPM Scientific Full time

    Job DescriptionJob Title: Clinical Trial Regulatory LeadCompany: EPM ScientificJob Type: Full-timeLocation: RemoteJob Category: PharmaceuticalAbout Us:EPM Scientific is a leading provider of scientific and regulatory services to the pharmaceutical industry. We are committed to delivering high-quality solutions that meet the evolving needs of our clients.Job...


  • Slough, Slough, United Kingdom EPM Scientific Full time

    Job DescriptionJob Title: Clinical Trial Regulatory LeadCompany: EPM ScientificJob Type: Full-timeLocation: RemoteJob Category: PharmaceuticalAbout Us:EPM Scientific is a leading provider of scientific and regulatory services to the pharmaceutical industry. We are committed to delivering high-quality solutions that meet the evolving needs of our clients.Job...


  • Slough, Slough, United Kingdom CK Group Full time

    Position Overview:CK Group is seeking a Clinical Trial Associate to support a prominent global pharmaceutical organization on a contractual basis.Compensation: Hourly rate: £20.03 PAYE or £27.27 via Umbrella.Key Responsibilities:Establish and maintain a comprehensive Trial Master File (TMF) Plan, ensuring thorough Quality Control (QC) checks throughout the...


  • Slough, Slough, United Kingdom EPM Scientific Full time

    About the RoleWe are seeking a highly experienced Clinical Development Lead to join our team at EPM Scientific. As a key member of our pharmaceutical development team, you will be responsible for overseeing the strategic planning, execution, and management of clinical development programs from early-stage development through to regulatory submission and...


  • Slough, Slough, United Kingdom EPM Scientific Full time

    About the RoleWe are seeking a highly experienced Clinical Development Lead to join our team at EPM Scientific. As a key member of our pharmaceutical development team, you will be responsible for overseeing the strategic planning, execution, and management of clinical development programs from early-stage development through to regulatory submission and...


  • Slough, Slough, United Kingdom Pharmiweb Full time

    Clinical Drug Delivery Device LeadPharmiweb is seeking a skilled Clinical Drug Delivery Device Lead to join our team. This role requires a professional to define and implement strategies for drug delivery devices used in clinical trials.As a Clinical Drug Delivery Device Lead, you will collaborate with a cross-functional team to ensure timely support and...


  • Slough, Slough, United Kingdom MSI Pharma Full time

    Job Summary:MSI Pharma is seeking a highly skilled Clinical Project Manager to lead Clinical Study Teams across Phase 1 studies. As a key member of our team, you will be responsible for overseeing the planning, execution, and delivery of clinical trials.Key Responsibilities:Study Planning and Execution: Develop and implement detailed study plans, ensuring...