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Study Startup Specialist I at PSI CRO

Ankara, Ankara, Turkey -

Full Time

Start Date

Immediate

Expiry Date

10 Aug, 26

Salary

0.0

Posted On

12 May, 26

Experience

0 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Clinical Research, Site Identification, Regulatory Review, Contract Negotiation, Budget Preparation, Communication, Organizational Skills, Relationship Building

Industry

Pharmaceutical Manufacturing

Description

Company 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. Job Description 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 Qualifications 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 Additional Information 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.

Responsibilities

The role involves supporting study startup processes, ensuring clinical projects start smoothly and on time. Responsibilities include site identification, document preparation for regulatory approval, and communication with various stakeholders.