PSI CRO
Pharmaceuticals
StudyStartupSpecialistII
Neural analysis suggests this role is
optimal for mid candidates.
“Study Startup Specialist II at PSI CRO. Skills: Study startup, Site activation, Document coordination. Collaborate with project team. Facilitate site agreement”
What You'll Achieve.
Ensure projects start smoothly; Ensure projects start on time; Meet site activation targets
Industry & Context.
Identify issues; Escalate issues
What They're Looking For.
Must Have
College/University degree in Life Sciences, 2 years Study Startup experience, Full professional working proficiency in English
Nice to Have
Build relationships at all levels
What You'll Do.
Collaborate with project team
Facilitate site agreement
Facilitate contract negotiations
Facilitate budget negotiations
Collect site documents
Coordinate translation
Coordinate review of documents
Identify project-specific issues
Escalate project-specific issues
Prepare study dossiers
Submit study dossiers
Prepare IP-REDs packages
Support distribution of Investigational Product
Support distribution of clinical study supplies
Ensure exchange of information
Ensure exchange of documentation
Participate in development of timelines
Participate in development of projections
Meet site activation targets
How You'll Work.
Team & Collaboration
Project team; Clinical research teams; Investigational sites; Off site facilities; Vendors
Process & Methodology
Study activation process
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. If you feel it is time to make your skills and knowledge visible within a growing company with true focus on its people, then PSI is the right choice for you. Take your career to the next level and lead challenging study activation process on a country level. You will support clinical research teams and ensure PSI projects start smoothly and on time. This is an office-based position from our Bangalore office. You will: * Collaborate with the project team for site activation processes * Facilitate site agreement, contract negotiations and budget negotiations * Collect site documents for IRB/IEC submission and/or IP-RED process * Coordinate translation and review of study-specific documents * Identify and escalate project-specific issues as needed * Prepare and submit the study dossiers to sites, competent authorities, IRBs/IECs * Prepare IP-REDs packages * Support initial distribution of Investigational Product(s) and clinical study supplies to sites * Ensure exchange of information and documentation with investigational sites, off site facilities and vendors * Participate in development of site-specific startup timelines and enrolment projections and is responsible for meeting the site activation targets ## Qualifications * College/University degree in Life Sciences or an equivalent combination of education, training and experience * At least 2 years of full-scope Study Startup experience in India-based trials * Full professional working proficiency in English * Well-developed communication and organizational skills * Ability to negotiate and build relationships at all levels ## Additional Information We offer: * Exce
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