Job Overview
Location
Remote, Turkey
Job Type
Full-time
Category
HR & Recruiting
Date Posted
April 14, 2026
Full Job Description
đź“‹ Description
- • As a Senior Clinical Research Associate at Precision Medicine Group, you will play a critical role in advancing oncology and rare disease therapies by ensuring clinical trials are conducted with the highest standards of quality, compliance, and scientific rigor. Your work directly contributes to bringing life-saving treatments to patients by monitoring study progress, safeguarding data integrity, and supporting protocol adherence across investigative sites.
- • Day to day, you will monitor and own the progress of clinical studies at investigative sites, ensuring adherence to protocol, SOPs, ICH-GCP, and regulatory standards. You will coordinate study setup activities including investigator identification, regulatory submissions, pre-study and initiation visits, and site management. You will also support Project Managers on larger trials, train and mentor junior CRAs, interact directly with clients, initiate payments, and participate in proposal development and client presentations.
- • Precision Medicine Group is a specialized CRO focused on precision medicine, particularly in oncology and rare diseases, with a culture centered on employee retention, meaningful impact, and work-life balance. Unlike larger CROs, we offer a collaborative environment where your voice is heard, you receive direct management support, and you can influence study outcomes and operational improvements. We pride ourselves on high CRA retention due to our people-first approach and enjoyable quality of life.
- • In this role, you will deepen your expertise in oncology and complex therapeutic areas, become a protocol expert through focused study ownership (1–2 studies at a time), and develop leadership skills by mentoring junior staff. You will gain experience in client-facing activities, proposal support, and study management, positioning you for advancement into lead CRA, project management, or medical monitoring roles within the organization.
🎯 Requirements
- • University degree in life science, pharmacy, or another health-related discipline, or equivalent experience in a scientific/healthcare field, or licensure as a healthcare professional
- • Minimum 3.5 years of experience as a CRA in a CRO, pharmaceutical, or biotech setting, with significant site management experience
- • Proven oncology monitoring experience
- • Excellent communication and organizational skills, with evidence of a client-focused approach
- • Proficiency in computerized information systems, electronic spreadsheets, word processing, and email
- • Ability to travel overnight, with up to 60% travel on average based on regional needs, including international travel as required
- • Fluency in both English and Turkish
🏖️ Benefits
- • Fully remote (home-based) work arrangement
- • High CRA retention rates reflecting a supportive, people-first culture and strong work-life balance
- • Opportunity to own and become an expert on one to two studies at a time, enabling deep protocol mastery
- • Direct influence and impact on study outcomes with support from accessible line management
- • Opportunities to train and mentor junior staff, participate in client proposals, and contribute to business development activities
- • Engagement in cutting-edge precision medicine work focused on oncology and rare diseases, combining advanced science, data analytics, and targeted trial design
Skills & Technologies
About Precision Medicine Group
Precision Medicine Group (PMG) is a leading life sciences consulting firm dedicated to accelerating the development and commercialization of precision medicine. They offer a comprehensive suite of services, including strategy, market access, regulatory affairs, and commercialization support. PMG partners with pharmaceutical, biotechnology, and diagnostic companies to navigate the complex landscape of personalized healthcare. Their expertise spans various therapeutic areas and advanced molecular technologies. By leveraging deep scientific knowledge and market insights, PMG helps clients optimize their drug development pipelines, secure regulatory approvals, and successfully launch innovative therapies. They are committed to advancing patient care through the power of precision medicine, ensuring that the right treatments reach the right patients at the right time.
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