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Premier Research Hiring for Clinical Research in Pune

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Premier Research

B.Pharm, M.Pharm, Pharm.D, Msc, BSc, Lifesciences, Other Clinical, Biological, or Nursing Science degrees

Pune

1 Years+

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Premier Research is inviting applications for the position of Site Solutions Executive (PRI) in Pune, India. This is an excellent opportunity for professionals interested in clinical research, clinical trial coordination, GCP compliance, eCRF management, and site operations.

The company is seeking candidates with backgrounds in life sciences, pharmacy, nursing, medicine, dentistry, biotechnology, or related clinical disciplines who are passionate about supporting innovative clinical trials and improving patient outcomes.

If you are looking for clinical research jobs in Pune, Site Solutions Executive jobs in India, or clinical trial coordinator vacancies, this opportunity offers strong career growth with a global CRO.


Job Details

ParticularDetails
PositionSite Solutions Executive (PRI)
CompanyPremier Research
LocationPune, Maharashtra, India
Job TypeFull-Time
Work ModeOffice-Based
DepartmentIndia Operations
Job IDR6265
Posted Date25 June 2026

About Premier Research

Premier Research is a global Contract Research Organization (CRO) supporting biotechnology, pharmaceutical, and medical device companies in developing innovative therapies. The organization partners with sponsors to deliver clinical research services while maintaining high standards of patient safety, regulatory compliance, and scientific excellence.


Key Responsibilities

As a Site Solutions Executive, your responsibilities include:

  • Coordinate day-to-day clinical trial activities at research sites.
  • Ensure compliance with study protocols, ICH-GCP guidelines, and local regulatory requirements.
  • Support Principal Investigators (PI) and site study teams.
  • Review existing site processes and identify operational improvements.
  • Perform accurate and timely Case Report Form (CRF) and Electronic Case Report Form (eCRF) data entry.
  • Maintain Trial Master File (TMF) and all essential clinical trial documentation.
  • Ensure documentation accuracy and regulatory readiness.
  • Support sponsor requirements and clinical monitoring activities.
  • Maintain patient safety and ethical standards throughout study execution.

Eligibility Criteria

Candidates should possess one of the following qualifications:

  • B.Pharm
  • M.Pharm
  • B.Sc Life Sciences
  • M.Sc Life Sciences
  • Biotechnology
  • Microbiology
  • Biochemistry
  • Nursing
  • MBBS
  • BDS
  • Medical or Dental Degree
  • Other Clinical, Biological, or Mathematical Science degrees

Candidates without the above qualifications should have at least 4 years of experience working at clinical research sites.


Required Skills

Applicants should demonstrate:

  • Strong English communication skills
  • Reading and writing proficiency in Hindi, Marathi, and English
  • Excellent coordination abilities
  • Organizational and documentation skills
  • Analytical and problem-solving abilities
  • Knowledge of Clinical Research processes
  • Familiarity with GCP guidelines
  • Understanding of CRF/eCRF documentation
  • Attention to detail
  • Computer proficiency including office communication tools

Preferred Candidate Profile

Premier Research is looking for professionals who are:

  • Detail-oriented
  • Patient-focused
  • Ethical and quality-conscious
  • Team players
  • Comfortable working in regulated clinical research environments
  • Passionate about improving healthcare through clinical trials

Why Join Premier Research?

Employees can expect:

  • Opportunity to work with global biotechnology and pharmaceutical companies
  • Exposure to international clinical research projects
  • Career development and training
  • Collaborative work environment
  • Work that directly contributes to improving patient lives
  • Stable career in a leading Contract Research Organization (CRO)

How to Apply

Application Link

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