Study Coordinator Professional
6 days ago
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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