Study Startup Specialist I

PSI CRO Ankara, tr Full-time Posted 21 July 2026
PharmaCROClinical ResearchRegulatory Affairscro

Job description

We are the company that cares – for our staff, for our clients, for our partners and for the quality of the work we do.  A dynamic, global company founded in 1995, we bring together more than 3,000 driven, dedicated and passionate individuals.  We work on the frontline of medical science, changing lives, and bringing new medicines to those who need them. Take your career to the next level and be involved in study startup processes in Türkiye. You will provide direct operational support to project teams and ensure that PSI clinical projects start smoothly and on time.  Office-Based in Ankara You will: Support site identification and selection process Collect and review documents for ethics and regulatory review and approval Prepare packages of site documents for drug release to clinical sites Prepare and negotiate site contracts and budgets Communicate with project teams, investigative sites, review bodies, vendors, and clients regarding startup matters till the moment of site activation Monitor startup metrics and timelines Coordinate initiatives for startup process improvement, analyze best practices and challenges College/University degree or an equivalent combination of education, training and experience At least 1 year industry experience in clinical research and/or a minimum 1 year of Study Startup experience in Türkiye Full working proficiency in English (B1) and C1 level in Turkish Communication and organizational skills Ability to negotiate and build relationships at all levels Make the right call and take your career to a whole new level.  Join the company that focuses on its people and invests in their professional development and success.

Stand out for this role

NoxPharm tailors your CV to this exact job description — matching the keywords recruiters and ATS systems screen for. Built for pharma & life sciences.

Tailor my CV now — free to try