Experienced Clinical Research Associate - Sponsor dedicated - Türkiye
IQVIA
Experienced Clinical Research Associate - Sponsor dedicated - Türkiye
Job Description
Clinical Research AssociateIQVIA Turkey is looking for talented and motivated team member to join our Sponsor dedicated team as experienced CRA's. At this position you will 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, and build a meaningful, strong career within our organization.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 and International Conference on Harmonization guidelinesManaging progress by tracking regulatory submissions, recruitment, case report form completion, and data query resolutionsCollaborating with experts at study sites and with client representativesQualifications:University degree in scientific discipline or health careRequires at least 6 months of on-site monitoring experience.Experience in Pharma Industry, and/or Clinical Trials environmentVery good computer skills including MS OfficeExcellent command of Turkish and English language, Turkey basedOrganizational, 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 knowledgeExcellent 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.This role is suitable for disabled individuals. Priority will be given to candidates registered with İŞKUR.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
- Pharma Industryintermediate
Required Qualifications
- University degree in scientific discipline or health care (degree in scientific discipline or health care)
- Requires at least 6 months of on-site monitoring experience. (experience)
- Experience in Pharma Industry, and/or Clinical Trials environment (experience)
- Very good computer skills including MS Office (experience)
- Excellent command of Turkish and English language, Turkey based (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)
- Requires at least 6 months of on-site monitoring experience. (experience)
- Experience in Pharma Industry, and/or Clinical Trials environment (experience)
- Very good computer skills including MS Office (experience)
- Excellent command of Turkish and English language, Turkey based (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 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
- 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
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: This role is suitable for disabled individuals. Priority will be given to candidates registered with İŞKUR.
- 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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