Study Coordinator Professional

6 days ago


Nottingham, Nottingham, United Kingdom Actalent Full time

Job Summary:

Actalent is seeking a highly skilled and experienced Clinical Research Coordinator to join our team. As a key member of our research team, you will be responsible for coordinating and managing clinical research studies, ensuring compliance with regulatory requirements and company policies.

Key Responsibilities:

  • Coordinate and manage clinical research studies, including study start-up, subject recruitment, and data collection.
  • Ensure compliance with regulatory requirements, including Good Clinical Practice (GCP) and Institutional Review Board (IRB) regulations.
  • Develop and maintain study protocols, case report forms, and other study-related documents.
  • Collaborate with cross-functional teams, including research scientists, clinicians, and data managers.
  • Provide training and support to research staff on study procedures and protocols.

Requirements:

  • Minimum 1 year of clinical research experience, preferably in oncology and hematology.
  • Strong knowledge of clinical research regulations, including GCP and IRB.
  • Excellent communication and project management skills.
  • Ability to work independently and as part of a team.

Preferred Qualifications:

  • Oncology and hematology experience.


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