Research Associate contributing to NIH - funded studies in Dr. Christina Dyar's lab. Managing operations and participant communications, while contributing to manuscripts and presentations.
About the role
- Experienced Clinical Research Associate working with sponsor dedicated team. Conducting site selection, monitoring, and collaboration with clinical experts to ensure regulatory compliance.
Responsibilities
- Performing site selection, initiation, monitoring and close-out visits
- Supporting the development of a subject recruitment plan
- Evaluating the quality and integrity of site practices in accordance with regulatory requirements, i.e., Good Clinical Practice and International Conference on Harmonization guidelines
- Managing progress by tracking regulatory submissions, recruitment, case report form completion, and data query resolutions
- Collaborating with experts at study sites and with client representatives
Requirements
- University degree in scientific discipline or health care
- Requires at least 6 months of on-site monitoring experience
- Experience in Pharma Industry, and/or Clinical Trials environment
- Very good computer skills including MS Office
- Excellent command of Turkish and English language
- Organizational, time management and problem-solving skills
- Ability to establish and maintain effective working relationships with co-workers, managers, and clients
- Flexibility to travel
- Driver’s license class B
Benefits
- Company car
- Mobile phone
- Attractive benefits package
- Resources that promote your career growth
- Leaders that support flexible work schedules
- Programs to help you build your therapeutic knowledge
- Excellent working environment in a stable, international, reputable company
Job title
Job type
Experience level
Salary
Not specified
Degree requirement
Location requirements
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