Medical Research Professional
2 weeks ago
We are seeking a highly motivated and experienced Medical Research Professional to join our team for a 2-year contract position. The ideal candidate will have extensive experience in clinical trials coordination and research administration.
About the Role:
Clinical Trials CoordinationKey Responsibilities:
- Coordinate and manage clinical trials from initiation to completion, ensuring compliance with regulatory requirements and Good Clinical Practice (GCP) guidelines.
- Develop and maintain effective relationships with investigators, sponsors, and other stakeholders to ensure timely and smooth trial conduct.
- Conduct site initiation visits, monitor and review study documents, and ensure compliance with study protocols and Standard Operating Procedures (SOPs).
- Manage and maintain accurate and up-to-date records and databases, including case report forms, informed consent forms, and adverse event reports.
- Collaborate with cross-functional teams to develop and implement operational strategies to improve trial efficiency and quality.
Requirements:
- Degree in medicine or a related field and a valid medical license.
- Minimum 2 years of experience in clinical trials coordination and research administration.
- Excellent communication and interpersonal skills, with the ability to work effectively with diverse stakeholders.
- Strong analytical and problem-solving skills, with the ability to think critically and make sound judgments.
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