PSI CRO
Pharmaceuticals
StudyStartupSpecialist
Neural analysis suggests this role is
optimal for mid candidates.
“Study Startup Specialist at PSI CRO. Skills: Study Startup processes, operational support, site identification and selection, 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 an”
What You'll Achieve.
ensure that PSI clinical projects start smoothly and on time; Monitor startup metrics and timelines
Industry & Context.
analyze best practices and challenges
What They're Looking For.
Must Have
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), C1 level in Turkish, Communication and organizational skills, Ability to negotiate and build relationships at all levels
What You'll Do.
provide direct operational support to project teams
ensure that PSI clinical projects start smoothly and on time
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
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
How You'll Work.
Team & Collaboration
Communicate with project teams; investigative sites; review bodies; vendors; clients regarding startup matters till the moment of site activation
Communication Scope
Communication and organizational skills; Communicate with project teams, investigative sites, review bodies, vendors, and clients regarding startup matters till the moment of site activation
Process & Methodology
process management, cross-functional coordination, vendor/stakeholder management, resource planning
Full 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 ## 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.
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