Clinical Research Associate – All Levels

🕒 January 20

🇹🇷 Turkey – Remote

⏰ Full Time

🟢 Junior

🟡 Mid-level

🧪 Clinical Research

👻 Ghost score 55%

What it means: how likely this posting is sitting open without active hiring.How to read it: 60% or higher means we think this is a ghost. Lower scores are less of a worry.How we score it: age, reposts, open roles vs team size, how fast jobs close, and whether pay is listed.Fine print: an estimate from public data, not a judgment of the company. Real jobs can score high, so treat it as a hint, not a fact.

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Thermo Fisher Scientific

WebsiteLinkedInAll Job Openings

10,000+ employees

Founded 1956

🏥 Healthcare

📦 Logistics

🏭 Manufacturing

Healthcare • Logistics • Manufacturing

Thermo Fisher Scientific is the world leader in serving science, with annual revenue of more than $40 billion. Their mission is to enable customers to make the world healthier, cleaner, and safer by supporting life sciences research, solving complex analytical challenges, increasing laboratory productivity, and improving patient health through diagnostics and the development of life-changing therapies. With a global team, they offer innovative technologies and pharmaceutical services through brands such as Thermo Scientific, Applied Biosystems, Invitrogen, Fisher Scientific, Unity Lab Services, Patheon, and PPD.

📋 Description

• Perform and coordinate clinical monitoring and site management activities • Conduct remote and on-site investigator site visits to assess protocol and regulatory compliance • Manage required clinical trial documentation and ensure audit readiness • Apply risk-based monitoring, root cause analysis, critical thinking, and problem-solving to identify site process failures and corrective/preventive actions • Ensure data accuracy through source document review, source data verification, and CRF review • Assess investigational product inventory and records • Document observations in reports and letters and escalate deficiencies to clinical management • Maintain contact with investigative sites between monitoring visits and follow up on issue resolution • Participate in investigator payment processes and investigator meetings • Identify potential investigators and initiate clinical trial sites according to applicable procedures • Perform trial closeout and retrieval of trial materials • Ensure essential documents are complete and compliant with ICH-GCP and regulations • Conduct on-site file reviews • Track trial status and provide progress updates • Maintain complete and accurate clinical trial management systems • Facilitate communication between investigative sites, clients, and internal project teams • Respond to regulatory requirements, audits, and inspections • Complete expense reports and timesheets • Contribute to project publications, tools, process improvements, and other project initiatives

🎯 Requirements

• Bachelor's degree in a life science-related field • 2+ years of independent on-site monitoring experience as a clinical research monitor, or comparable clinical monitoring experience • Clinical trial, medical terminology, medical research, clinical research, health care, or health sciences experience • Formal training in medical terminology and anatomy may be considered • Proven understanding of ICH-GCP, EU and FDA requirements • Understanding of medical/therapeutic area knowledge and medical terminology • Fluent in English and Turkish • Valid driver's license where applicable • Must be based in Türkiye • Good knowledge of Microsoft Office and ability to learn appropriate software • Ability to manage Risk Based Monitoring concepts and processes • Ability to maintain knowledge of ICH GCPs, applicable regulations, and procedural documents • Good English language and grammar skills • Critical thinking, root cause analysis, and problem-solving skills • Organizational and time management skills • Ability to work independently and in a team • Ability to communicate effectively with medical personnel • Flexibility and adaptability

🏖️ Benefits

• Competitive salary • Award-winning learning and development programme • Flexible working culture • Work-life balance • Health and well-being benefits package • Collaborative environment • Opportunities to grow professionally and personally • Global organization with a local feel