Clinical Research Manager
2 months ago
**About the Role**
We are seeking a highly skilled and experienced Trial Manager to join our team at LSTM. As a key member of our clinical research team, you will be responsible for the day-to-day management of clinical trials, ensuring that they are conducted in accordance with Good Clinical Practice (GCP) guidelines and regulatory requirements.
**Key Responsibilities**
- Manage and coordinate clinical trials from initiation to close-out, including site selection, patient recruitment, and data management.
- Develop and maintain trial protocols, case report forms, and other trial-related documents.
- Collaborate with cross-functional teams, including research scientists, clinicians, and regulatory affairs specialists.
- Ensure compliance with regulatory requirements, including ICH-GCP, FDA, and EMA guidelines.
- Conduct site visits and monitor trial progress to ensure quality and integrity.
**Requirements**
- Proven experience in clinical trial management, preferably in a pharmaceutical or biotechnology company.
- Strong knowledge of GCP, regulatory requirements, and clinical trial protocols.
- Excellent communication and project management skills.
- Ability to work independently and as part of a team.
**What We Offer**
LSTM offers a competitive salary and benefits package, as well as opportunities for professional growth and development. If you are a motivated and experienced Trial Manager looking for a new challenge, please submit your application.
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