We are looking for a highly skilled and experienced Clinical Trial Administrator to join our team at Ruputed Pharmaceutical Company. The ideal candidate will have a robust background in the pharmaceutical industry, with experience in clinical trials administration.
Roles and Responsibility
- Manage and coordinate clinical trial activities, including protocol development and study execution.
- Collaborate with cross-functional teams, including data management, biostatistics, and medical writing.
- Develop and maintain clinical trial documentation, including protocols, informed consent forms, and case report forms.
- Ensure compliance with regulatory requirements and company policies.
- Coordinate with external stakeholders, including CROs, laboratories, and other vendors.
- Analyze and resolve issues related to clinical trial conduct or delivery.
Job Requirements
- Bachelor's degree in life sciences or a related field.
- Minimum 2 years of experience in clinical trials administration or a related field.
- Strong knowledge of Good Clinical Practice (GCP) principles and regulations.
- Experience with clinical trial management systems (CTMS) and electronic data capture (EDC).
- Excellent communication and project management skills.
- Ability to work in a fast-paced environment and meet deadlines.