Synergen Bio Hiring Research Associate – Project Management, Biopharmaceutical

MBA BPharm RA Jobs 2 Vacancies Pune CRO

MBA, B.Pharm, M.Pharm candidates apply for 2 Research Associate vacancies in Clinical CRO projects at Synergen Bio Pune.

If you are looking to build a career in clinical research, CRO services, and pharmaceutical project management, this opportunity at Synergen Bio is a strong entry point. The company is hiring Research Associates for Project Management and Biopharmaceutical roles, offering exposure to clinical trials, regulatory coordination, and sponsor communication.

This role is ideal for candidates searching for clinical research jobs, CRO jobs in Pune, BA/BE study roles, or pharmaceutical project management careers with regulatory exposure like DCGI submissions.

Company Overview

Synergen Bio is a growing Contract Research Organization (CRO) focused on delivering high-quality clinical research and biopharmaceutical services. The company supports sponsors with BA/BE studies, regulatory submissions, and project execution aligned with global and Indian regulatory frameworks.

With a strong emphasis on compliance, documentation, and project timelines, Synergen Bio contributes to accelerating drug development and ensuring safe, effective therapies reach the market.

Job Role & Responsibilities

Research Associate – Project Management & Biopharmaceutical

• Act as a key communication bridge between sponsors and internal project teams
• Support CRO operations including BA/BE studies and clinical project coordination
• Monitor project timelines, deliverables, and ensure adherence to agreed milestones
• Coordinate with cross-functional teams including clinical, analytical, and regulatory units
• Prepare and review SOPs, service agreements, and confidential project documents
• Assist in DCGI NOC submissions for BA/BE studies and regulatory approvals
• Track project progress and provide updates to management
• Resolve project-related queries in coordination with stakeholders

This role plays a critical part in ensuring smooth execution of clinical research projects and regulatory compliance.

Eligibility / Qualifications

Required Education:

• MBA
• B.Pharm
• M.Pharm

Relevant Courses:

Clinical Research, Pharmaceutical Management, Regulatory Affairs, Pharmacology, Biopharmaceutics, Clinical Data Management, Project Management, Drug Development, GMP, GCP, GLP

Experience Required:

• 2 to 4+ years in CRO / clinical research / project coordination roles

Skills Required:

• Strong communication and stakeholder management skills
• Knowledge of BA/BE studies and CRO operations
• Understanding of DCGI regulations and submissions
• Documentation and SOP preparation expertise
• Project tracking and coordination skills

Location & Salary

• Location: Pune, Maharashtra
• Salary: Competitive and aligned with industry standards
• Opportunity: Work in CRO environment with exposure to clinical trials and regulatory frameworks

Application Process

Interested candidates who can join immediately are strongly encouraged to apply.

Apply Now:

• Email: careers@synergenbio.com

Make sure your resume highlights your clinical research experience, project coordination skills, and regulatory exposure.

Apply early to increase your chances of selection.

Why Join Synergen Bio?

• Direct exposure to CRO services and clinical trial operations
• Opportunity to work on BA/BE studies and DCGI regulatory submissions
• Strong career path in pharmaceutical project management and clinical research
• Hands-on experience in cross-functional coordination and sponsor communication

This role contributes to faster drug approvals and ensures clinical research compliance, directly impacting patient safety and healthcare advancements.

FAQs

Who can apply for this role?

Candidates with MBA, B.Pharm, or M.Pharm with relevant CRO or project management experience.

Is experience mandatory?

Yes, candidates should have at least 2 years of relevant experience.

What type of projects will I work on?

Primarily BA/BE studies, clinical research projects, and regulatory submissions.

What regulatory exposure is required?

Basic understanding of DCGI processes and clinical documentation.

How to apply?

Send your updated resume to the provided email ID.

Final Thoughts

This Synergen Bio recruitment drive is a high-value opportunity for professionals aiming to grow in clinical research and CRO project management. With direct exposure to regulatory processes and sponsor coordination, this role offers strong long-term career growth.

If you meet the criteria, apply immediately.

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Company	Synergen Bio
Vacancies	Research Associate – Project Management, Biopharmaceutical
Required Education	MBA, B.Pharm, M.Pharm
Experience	2–4+ Years