Clinical Research Associate Job at Precision For Medicine, Türkiye | Life Sciences
If you are an experienced clinical operations professional with a background in oncology monitoring looking to step into a specialized role with an industry-leading quality of life, this opportunity at Precision for Medicine is an exceptional find. Located in the prominent commercial district of Beşiktaş, Istanbul, this position offers the flexibility of being fully home-based within Türkiye. For clinical trial experts searching for a high-value Clinical Research Associate Job, this position stands out by limiting your focus to an average of just one to two specific protocols, allowing you to become a true therapeutic expert. It serves as an elite launchpad for a long-term career in precision therapeutics and is a premier choice for anyone tracking a flexible, high-retention Job in Türkiye or a competitive Life Sciences Job in the region.
- Job Position: Clinical Research Associate I/ Clinical Research Associate II
- Location: Besiktas, Istanbul, Türkiye
About The Company
Precision for Medicine is not your typical Contract Research Organization (CRO). As part of the Precision Medicine Group, the company specializes in shifting the standard clinical trial paradigm by combining novel trial designs, industry-leading operational and medical experts, and advanced biomarker and data analytics solutions. The organization focuses intensely on rare diseases and cutting-edge oncology breakthroughs, striking tumors on a molecular level by linking specific mutations to targeted treatments.
Unlike larger, highly transactional CROs, Precision for Medicine is deeply passionate about cultivating an internal culture that respects work-life balance. This deliberate focus has resulted in exceptionally high CRA retention rates that track well above the industry average. Working here gives you the backing of a global precision medicine leader while ensuring your voice is heard directly by line management.
Clinical Research Associate Job – Key Responsibilities
As a CRA I or CRA II, you will take full operational ownership of monitoring clinical studies at investigative sites, ensuring that all data endpoints are recorded and reported in strict compliance with protocols, corporate SOPs, and international guidelines.
Your core monitoring, regulatory, and risk-mitigation duties include:
- End-to-End Site Progress Monitoring: Owning the continuous progress of complex clinical trials at assigned investigative sites to ensure strict alignment with Study Protocols, SOPs, ICH-GCP, and local regulatory criteria.
- Oncology & Target Assay Verification: Auditing source documentation and electronic case report forms (eCRFs) for specialized oncology trials, tracking biomarkers, and assessing targeted endpoints to advance this Clinical Research Associate Job.
- Comprehensive Site Lifecycles: Coordinating all baseline activities required to set up and run a trial, including identifying investigators, executing pre-study assessments, conducting site initiation visits (SIVs), routine interim monitoring (IMVs), and site close-out visits (COVs).
- Regulatory Submission Support: Assisting regional teams in compiling, reviewing, and preparing localized regulatory submissions for ethics committees and health authorities to support this Job in Türkiye.
- Risk Mitigation & Resolution: Proactively identifying potential site-level study risks, proposing actionable data-driven solutions, and using proven resolution strategies to handle site conflict or compliance anomalies.
- Stakeholder Correspondence: Establishing professional relationships with principal investigators and clinical research coordinators to maintain high enrollment predictability and data entry compliance for this Life Sciences Job.
Qualifications & Profile Requirements For Clinical Research Associate Job
Precision for Medicine seeks thoughtful, highly responsive communicators who stay two steps ahead of trial issues, exhibit an impeccable eye for detail, and take real responsibility for the quality of their work.
- Required Academic & Experience Criteria:
- Educational Foundation: A formal University degree in life science, OR an equivalent combination of healthcare certifications and clinical experience.
- Experience Tier: A minimum of 6 months of direct experience as a CRA operating within either a CRO, pharmaceutical, or biotechnology industry setting.
- Therapeutic Focus: Proven tracking and independent monitoring experience within the Oncology therapeutic area is required.
- Linguistic Mastery: Full professional fluency in both English and Turkish (written and verbal) is essential to handle localized country documentation and global sponsor updates.
- Technical & Mobility Competencies:
- Strong command of computerized information systems, electronic spreadsheets (Excel), word processing software, and electronic mail clients.
- Absolute flexibility to travel overnight. This position averages up to 60% regional travel based on protocol requirements, alongside occasional international travel as needed.
- Excellent interpersonal, team-player, and client-focused communication habits.
- Preferred Asset: Prior experience handling site start-up activities, ethical onboarding, or clinical trial activations.
In short, the Clinical Research Associate I/II position at Precision for Medicine is a definitive route to transitioning your oncology monitoring background into a highly rewarding corporate asset. Securing an appointment here allows you to escape high-turnover, multi-protocol corporate frameworks and focus deeply on the precision biomarkers and site relationships that bring groundbreaking cancer therapies to reality. If you reside in Türkiye, meet the 6-month oncology CRA baseline, and possess an compromise-free commitment to GCP standards, apply today in English to secure this premier Clinical Research Associate Job, launch a highly rewarding Job in Türkiye, and lock in this outstanding Life Sciences Job.
