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Clinical Research Associate

2 months 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.
  • Monitor and report adverse events, and ensure timely resolution of queries.
  • Perform data entry and administrative tasks, including data cleaning and quality control.

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 interpersonal skills, with ability to work independently and as part of a team.
  • Strong organizational and time management skills, with ability to prioritize tasks and meet deadlines.

Preferred Qualifications:

  • Oncology and hematology experience.