Assistant Clinical Research Job | B.Pharm & M.Pharm

Assistant Clinical Research Job: Looking to start your career in Clinical Research? Fortis Healthcare Ltd. is hiring Assistant Clinical Research professionals for its Gurugram location. This is an excellent opportunity for B.Pharm and M.Pharm freshers or candidates with up to 1 year of experience who are interested in clinical trials, GCP guidelines, medical writing, data management, and research documentation. Pharmaacademias.com

If you are passionate about clinical research and want to work with one of India’s leading healthcare organizations, this opportunity could be the perfect start for your career.

Job Overview

About Fortis Healthcare

Fortis Healthcare is one of India’s leading integrated healthcare service providers, operating a network of multi-specialty hospitals across the country. The organization is recognized for delivering high-quality patient care while actively contributing to clinical research and medical innovation.

Working at Fortis offers professionals the opportunity to gain hands-on experience in clinical research, collaborate with experienced healthcare experts, and build a rewarding career in the pharmaceutical and healthcare industry.

Job Description

Fortis Healthcare is seeking a highly motivated, detail-oriented, and enthusiastic Assistant Clinical Research professional to support its clinical research team.

The selected candidate will assist in planning, coordinating, documenting, and monitoring clinical research activities while ensuring compliance with Good Clinical Practice (GCP) guidelines and applicable regulatory requirements.

This role provides excellent exposure to clinical trial operations, research methodology, quality assurance, medical writing, and cross-functional collaboration.

Key Responsibilities

As an Assistant Clinical Research professional, your responsibilities will include:

• Assist in the development and implementation of clinical trial protocols.
• Support study planning and research methodology.
• Coordinate with cross-functional teams including:
  • Data Management
  • Biostatistics
  • Medical Writing
  • Clinical Operations
• Conduct scientific literature reviews for ongoing and upcoming studies.
• Analyze research information to support protocol development.
• Maintain accurate clinical trial documentation.
• Prepare and organize essential study records.
• Track study progress and ensure documentation is updated.
• Collaborate with investigators and clinical site staff.
• Ensure adherence to study protocols and regulatory guidelines.
• Assist with Quality Control (QC) and Quality Assurance (QA) activities.
• Support compliance with Good Clinical Practice (GCP).
• Participate in internal meetings and project discussions.

Eligibility Criteria

Candidates should possess:

• Bachelor’s degree in Life Sciences or related discipline.
• B.Pharm graduates are eligible.
• M.Pharm candidates are also eligible.
• Freshers or candidates with up to 1 year of experience are encouraged to apply.

Required Skills

The ideal candidate should have knowledge of:

• Clinical Research
• Clinical Trials
• Good Clinical Practice (GCP)
• Regulatory Compliance
• Medical Writing
• Data Management
• Literature Review
• Research Methodology
• Quality Assurance (QA)
• Quality Control (QC)
• Documentation Management
• Communication Skills
• Analytical Thinking
• Problem Solving
• Team Collaboration
• Healthcare Research

Preferred Qualifications

Candidates having exposure to the following will have an added advantage:

• Clinical trial databases
• Electronic data capture (EDC) systems
• Research documentation
• Hospital-based clinical research
• Regulatory submissions
• Study coordination

Why Join Fortis Healthcare?

Working at Fortis Healthcare offers numerous career advantages:

• Opportunity to work with one of India’s leading hospital chains.
• Excellent learning environment for freshers.
• Exposure to real-world clinical trials.
• Experience with GCP-compliant research.
• Collaboration with experienced clinicians and researchers.
• Career growth in Clinical Research and Clinical Operations.
• Hands-on experience in research documentation and study coordination.
• Strong foundation for future roles in CROs, pharmaceutical companies, and healthcare organizations.

Career Growth Opportunities

This position can help you advance into roles such as:

• Clinical Research Coordinator (CRC)
• Clinical Trial Associate (CTA)
• Clinical Research Associate (CRA)
• Clinical Data Coordinator
• Medical Writer
• Pharmacovigilance Associate
• Regulatory Affairs Executive
• Clinical Project Coordinator
• Clinical Operations Associate

Salary

• Salary: Not Disclosed
• Compensation will be based on company policy, qualifications, and experience.

Job Location: Gurugram, Haryana

Who Should Apply?

This opportunity is ideal for:

• B.Pharm Freshers
• M.Pharm Freshers
• Life Science Graduates
• Candidates looking to enter Clinical Research
• Professionals with up to 1 year of clinical research experience
• Candidates interested in hospital-based research careers

How to Apply?

Interested candidates should apply through the official Fortis Healthcare careers portal or the relevant recruitment platform where the vacancy is listed. Ensure that your updated resume highlights your educational qualifications, internships, research projects, GCP knowledge, and relevant technical skills.

Important Disclaimer

Disclaimer: This job posting has been aggregated from an external source for informational purposes only. Job role, eligibility criteria, responsibilities, and availability may change without prior notice. Candidates are strongly advised to verify the latest information and submit their applications through the official Fortis Healthcare careers website before applying.

Editorial Note

This article has been carefully researched and written by Deepak Rajput with a focus on accuracy, clarity, and evidence-based healthcare information.