You will help biotech, medtech, and specialty pharma companies transform life-changing ideas and breakthrough science into new medicines, devices, and diagnostics. What we do is profoundly connected to saving and improving lives, and we recognize our team members are the most valuable asset in delivering success.
We are here to help you grow, to give you the skills and opportunities to excel at work with the flexibility and balance your life requires.
Your ideas influence the way we work, and your voice matters here.
As an essential part of our team, you help us deliver the medical innovation that patients are desperate for.
Join us and build your future here.
Coordinates and facilitates all Clinical trial activities at site ensuring compliance with protocol, applicable GCP guidelines and local regulations.
Supports Principal Investigator (PI) and site study team assuring that the clinical trial(s) being conducted meet all the criteria set by the sponsors and regulators,
Reviews the site processes, identifies gaps and supports roll-out of site processes.
The following key functions are required routinely: Performs timely data entry of the Case Record Forms (CRF) or Electronic CRF (eCRF) in consultation with the PI/Investigator Maintaining clinical trial-related documents at site including Trial Master File.
What we are looking for:
A bachelor’s or master’s degree in clinical, biological or mathematical sciences or related fields, or a medical or dental degree or a nursing qualification; Exceptions to this would require a minimum of 4 years of experience of working at clinical research sites.
Good oral and written communication skills in English and at least one local Indian language
Excellent interpersonal skills
Good coordination and organizational skills and also problem-solving and analytical skills
Attention to detail and documentation and conscious of the importance of time and data accuracy in the clinical trial context
Conscious of ethical and scientific requirements and of patient-safety and patient-rights in the clinical trial context
Familiarity with computer usage and office communication tool
A successful candidate must be able to start this role by 22 June 2026 and must possess both reading and writing proficiency in Hindi and English.
Skills Required
- Bachelor's or master's degree in clinical, biological or mathematical sciences or related fields
- Good oral and written communication skills in English and a local Indian language
- 4 years of experience in clinical research sites (if no degree)
- Excellent interpersonal, coordination, organizational, problem-solving, and analytical skills
- Attention to detail and accuracy in clinical trial context
What We Do
We’re out to change the course of medical science. Are you ready to rise to the challenge? Premier Research is not about being everything to everyone. Instead, our deep, focused expertise targets the therapeutic areas and indications where today’s biotech and specialty pharma pioneers are doing the most amazing work. We’re 1,500 employees strong and operate in more than 20 countries, delivering unmatched expertise, operational skills, and dedication to meeting customers’ most challenging needs. Join us and meet some of the brightest minds in clinical development today — people who apply their best thinking to every project, recognizing that what they do significantly affects the lives and well-being of customers, patients, physicians, and colleagues. You’ll enjoy great benefits and very flexible working conditions in a company that values your contributions, rewards your achievements, and is committed to helping you reach your full potential. Are you ready to make a real difference and help us transform this exciting industry? Follow our company page for more information about us and the work we do, and check out our current openings for your next career move!
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