Clinical Research Job at Parexel Turkey
Looking for a rewarding Clinical Research Job in Turkey? Join Parexel as a Clinical Research Associate (CRA/CRAII) and play a pivotal role in advancing patient care through global clinical trials. This opportunity offers excellent jobs in Turkey, flexible responsibilities, and a strong jobs opportunity for life science graduates seeking professional growth within a world-leading CRO.
About Parexel
Parexel is a global contract research organization (CRO) delivering high-quality clinical trials across multiple therapeutic areas. Known for offering top Clinical Research Jobs worldwide, Parexel supports jobs in Turkey and provides strong jobs opportunities for life science graduates. With a collaborative and innovative environment, Parexel is a premier destination for CRAs seeking global exposure and professional growth.
Job Details:
- Job Title: Clinical Research Associate (CRA/CRAII)
- Job ID: R0000037035
- Category: Clinical Trials
Clinical Research Job Overview
The Clinical Research Associate (CRA) at Parexel plays a critical role in advancing treatments to patients safely and efficiently. CRAs prioritize patient safety and well-being while performing monitoring duties at investigator sites. The role requires inquisitiveness, accountability, integrity, and strong interpersonal skills to build relationships with study sites and cross-functional teams.
The Senior CRA contributes to global clinical trials across multiple therapeutic areas and supports site operations to ensure high-quality data and compliance with all relevant guidelines.
Key Responsibilities
Site Management
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Contribute to the selection of potential investigators and site qualification visits.
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Manage study start-up and regulatory maintenance, including submission of documents to EC/IRB and Regulatory Authorities.
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Train, advise, and support investigators and site staff on study-related matters and Risk-Based Quality Management (RbQM) principles.
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Ensure site staff complete and document required training, including ICH-GCP, and maintain inspection readiness.
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Participate in Local Study Team (LST) meetings and National Investigator meetings as applicable.
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Initiate, monitor, and close study sites according to client procedures. Share updates on patient recruitment and site performance.
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Drive site performance, proactively resolving study-related issues, and escalating as appropriate.
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Update CTMS and other systems with site data within required timelines.
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Manage study supplies, drug accountability, and preparation for drug destruction when needed.
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Conduct on-site and remote monitoring visits, data checks, and Source Data Verification (SDV) per the Monitoring Plan.
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Perform regular Site Quality Risk Assessments and adjust monitoring intensity accordingly.
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Ensure timely resolution of data queries and collaborate with data management for quality data.
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Report Serious Adverse Events (SAEs) accurately and promptly.
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Prepare monitoring visit reports in CTMS, providing timely feedback to the Principal Investigator.
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Assist sites in maintaining inspection-ready Investigator Site Files (ISF) and preparing for audits or regulatory inspections.
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Ensure timely collection and upload of essential documents into eTMF.
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Provide relevant local research intelligence, including competitor and investigator insights.
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Collaborate with local Medical Scientific Liaisons (MSLs) as directed.
Compliance Responsibilities
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Ensure adherence to the client’s Code of Ethics, company policies, and applicable local/national regulations.
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Complete timesheets, expense reports, and required training accurately.
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Maintain knowledge of Parexel/Client processes, ICH-GCP, and other regulatory requirements.
Skills & Competencies
Essential Skills
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Excellent attention to detail.
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Strong written and verbal communication.
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Effective collaboration and interpersonal skills.
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Negotiation capabilities.
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Proficiency in English and local languages.
Desirable Skills
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Ability to work with remote collaborators and manage change positively.
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Ability to identify more efficient and effective clinical trial methods.
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Analytical and problem-solving skills.
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Ability to prioritize multiple tasks with conflicting deadlines.
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Understanding of technology’s impact on clinical trials and ability to use e-enabled systems.
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Team-oriented, flexible, and able to adapt to shifting demands.
Knowledge & Experience for Clinical Research Job
Essential
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In-depth knowledge of ICH-GCP, with basic understanding of GMP/GDP.
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Understanding of local regulations and clinical trial requirements.
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Good medical knowledge, with the ability to learn client therapeutic areas.
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Basic knowledge of drug development processes and Clinical Study Management, including monitoring, drug handling, and data management.
Desirable
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Familiarity with risk-based monitoring approaches, including remote monitoring.
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Cultural awareness for international collaboration.
Education & Qualifications
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Bachelor’s degree in Life Sciences or a related discipline, or equivalent qualification aligned with local market needs.
Additional Requirements
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Ability to travel nationally and internationally as required.
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Valid driving license per local country regulations.
