Research Analyst at KBS Corporate identifying and contacting potential buyers for client businesses. Engaging in research strategies and liaising with buyers and clients for business acquisitions.
About the role
- Senior Clinical Research Associate responsible for site monitoring and compliance in clinical research with IQVIA. Join a reputable global provider of clinical research services.
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 (GCP) and International Conference on Harmonization (ICH) guidelines
- Managing progress by tracking regulatory submissions, recruitment, case report form (CRF) completion, and data query resolution
- Collaborating with experts at study sites and with client representatives
Requirements
- University degree in scientific discipline or health care
- At least 2 years of on-site monitoring experience
- Good knowledge of clinical research regulatory requirements
- 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
- Resources that promote your career growth
- Leaders that support flexible work schedules
- Programs to help you build your therapeutic knowledge
- Better Work-Life balance, optimal DOS
- Excellent working environment in a stabile, international, reputable company
- Company car, mobile phone and attractive benefits package
Job title
Job type
Experience level
Salary
Not specified
Degree requirement
Tech skills
Location requirements
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