Senior Clinical Research Associate
IQVIA is the Human Data Science Company oriented to drive human health outcomes forward.
When you join IQVIA Turkey as a sponsor-dedicated CRA, you’ll enjoy the stability and resources of a leading, global contract research organization while gaining direct experience with one of our customers.
With access to world-class training and mentoring, you’ll have the opportunity to put your passions to work in an environment designed to help you gain experience in a wide variety of therapeutic areas.
Your responsibilities will include:
-
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
Qualifications:
-
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
What you can expect:
- 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