(Senior) Clinical Research Associate - Sponsor dedicated - Türkiye
IQVIA
(Senior) Clinical Research Associate - Sponsor dedicated - Türkiye
Job Description
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 visitsSupporting the development of a subject recruitment planEvaluating the quality and integrity of site practices in accordance with regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelinesManaging progress by tracking regulatory submissions, recruitment, case report form (CRF) completion, and data query resolutionCollaborating with experts at study sites and with client representativesQualifications:University degree in scientific discipline or health careAt least 2 years of on-site monitoring experienceGood knowledge of clinical research regulatory requirementsVery good computer skills including MS OfficeExcellent command of Turkish and English languageOrganizational, time management and problem-solving skillsAbility to establish and maintain effective working relationships with co-workers, managers, and clientsFlexibility to travelDriver’s license class BWhat you can expect: Resources that promote your career growthLeaders that support flexible work schedulesPrograms to help you build your therapeutic knowledgeBetter Work-Life balance, optimal DOSExcellent working environment in a stabile, international, reputable companyCompany car, mobile phone and attractive benefits packageFor candidates able to start before September 2026, a discretionary sign‑on bonus of up to 210,000 TRY may be offered, with the final amount confirmed at offer stage, subject to role level and relevant experience.IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.comIQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.
Locations
- Turkey, Istanbul
- Turkey, Istanbul
Skills Required
- clinical research regulatory requirementsintermediate
Required Qualifications
- University degree in scientific discipline or health care (degree in scientific discipline or health care)
- At least 2 years of on-site monitoring experience (experience, 2 years)
- Good knowledge of clinical research regulatory requirements (experience)
- Very good computer skills including MS Office (experience)
- Excellent command of Turkish and English language (experience)
- Organizational, time management and problem-solving skills (experience)
- Ability to establish and maintain effective working relationships with co-workers, managers, and clients (experience)
- Flexibility to travel (experience)
- Driver’s license class B (experience)
- University degree in scientific discipline or health care (degree in scientific discipline or health care)
- At least 2 years of on-site monitoring experience (experience, 2 years)
- Very good computer skills including MS Office (experience)
- Excellent command of Turkish and English language (experience)
- Organizational, time management and problem-solving skills (experience)
- Ability to establish and maintain effective working relationships with co-workers, managers, and clients (experience)
- Flexibility to travel (experience)
- Driver’s license class B (experience)
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
- 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
Benefits
- general: For candidates able to start before September 2026, a discretionary sign‑on bonus of up to 210,000 TRY may be offered, with the final amount confirmed at offer stage, subject to role level and relevant experience.
- general: IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com
- general: IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.
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