Study Startup Specialist II

PSI CRO·Bengaluru, Karnataka, India

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About the role

Office-based Study Startup Specialist II role in Bengaluru supporting country-level clinical study activation. Responsibilities include site agreements, contract and budget negotiations, regulatory and IRB/IEC submissions, IP-RED packages, document coordination, supply distribution, vendor communication, and meeting activation targets. Requires a college/university degree in Life Sciences or an equivalent combination of education, training and experience, at least two years of full-scope study startup experience in India-based trials, and full professional working proficiency in English.

Key requirements

• College/University degree in Life Sciences or an equivalent combination of education, training and experience
• At least 2 years of relevant experience
• Required skills: Full-scope study startup experience in India-based trials, Site activation processes, Site agreement and contract negotiation, Budget negotiation, IRB/IEC submission documentation, IP-RED process documentation, Study document coordination and review, Study dossier preparation and submission, Investigational Product and clinical study supply distribution, Site and vendor communication, Startup timeline and enrolment projection development, Communication skills, Organizational skills, Negotiation and relationship-building skills
• Required language: English

Opportunity details

• Workplace: On Site
• Posted: Aug 17, 2026
• Original advert language: English

Full vacancy

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Employer’s role description

Job title: Study Startup Specialist II

Location: Bengaluru, KA, India

Employment type: Full-time

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.

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.

Job Description

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:

Excellent working conditions
Extensive training and friendly team
Competitive salary and benefits package
Opportunities for personal and professional growth

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.