Senior Study Startup Specialist at PSI CRO

Ankara, Ankara, Turkey -

Full Time

Start Date

Immediate

Expiry Date

21 Apr, 26

Salary

0.0

Posted On

21 Jan, 26

Experience

5 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Clinical Research, Study Startup, Project Management, Regulatory Compliance, Document Management, Negotiation, Communication, Organizational Skills, Translation Review, Site Activation, Budget Negotiation, Timelines Development, Problem Solving, Team Support, Investigational Products, IRB Submission

Industry

Pharmaceutical Manufacturing

Description

Company Description PSI is a leading Contract Research Organization with 30 years experience in the industry, offering a perfect balance between stability and innovation to both clients and employees. We focus on delivering quality and on-time services across a variety of therapeutic indications. 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, ensure that clinical projects start smoothly and on time and support PSI in developing the local study startup team. Office-based in Ankara or remote Perform study startup activities and support all processes critical for site activation. Collect site documents for IRB/IEC submission and/or IP-RED process. File study-specific documentation in TMF, in accordance with Document management plan. Compile IP-REDs packages assuring high quality. Review study-specific translations, including patient-facing documents. Support site agreement and/or budget negotiations, upon request. Ensure initial distribution of locally obtained clinical study supplies to sites and supervise initial distribution of Investigational Product(s) and centrally obtained clinical study supplies to sites. Identify project-specific issues and escalates to Regional (Startup) Lead/PM and operational Manager in the country. Develop site-specific startup timelines and is responsible for meeting the site activation targets under supervision. Qualifications College/University degree or an equivalent combination of education, training and experience At least 4 years' experience in clinical research At least 3 years of full-scope Study Startup experience in Türkiye Excellent knowledge of ICH GCP, local laws and applicable regulations in the region Full working proficiency in English and 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 Senior Study Startup Specialist will perform study startup activities and support processes critical for site activation. They will ensure clinical projects start smoothly and on time while developing the local study startup team.