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Synergen Bio Hiring Clinical Research Associate (CRA) – Clinical Trials & BA/BE Jobs

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Explore clinical research associate jobs in pharma CRO at Synergen Bio Pvt. Ltd. CRA roles in Pune for BA/BE studies. 1-2+ years experience required—immediate joiners preferred!

About the Company

Synergen Bio Private Limited is a DCGI-approved full-service Contract Research Organization (CRO) based in Pune, India. Established in 2018, it specializes in clinical trials (Phase I-IV), bioavailability/bioequivalence (BA/BE) studies, bioanalytical services, and regulatory support.

With state-of-the-art infrastructure, including a 160-bed clinical unit and GLP-compliant labs, Synergen Bio serves pharmaceutical and biotechnology clients globally. The company emphasizes quality, scientific expertise, regulatory compliance, and timely delivery to accelerate drug development.

Job Details

  • Company Name: Synergen Bio Pvt. Ltd.
  • Experience: 1-2+ Years
  • Qualification: M.Sc., B.Pharm
  • Location: Shivajinagar, Wakadewadi, Pune, Maharashtra
  • Work Type: On-site

Job Description

Synergen Bio is hiring Clinical Research Associates to support bioavailability/bioequivalence (BA/BE) studies and clinical operations.

This role offers hands-on involvement in study execution, documentation, and regulatory compliance. Join a growing CRO committed to quality clinical research.

Clinical Research Associate (CRA)

  • Department: Clinical Research
  • Role: Clinical Research Associate (BA/BE Studies)
  • Experience: 1-2+ Years
  • Education/Qualification: M.Sc., B.Pharm

Skills/Qualifications

  • Strong knowledge of SOPs and regulatory guidelines (ICH-GCP, DCGI)
  • Experience in BA/BE or clinical trial execution
  • Proficiency in document management and review
  • Excellent attention to detail and organizational skills
  • Ability to handle informed consent and screening activities
  • Good communication for training and stakeholder updates
  • Commitment to quality compliance
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Key Responsibilities

  • Execute BA/BE studies per SOPs and regulations
  • Prepare and compile Trial Master File documents
  • Review CRFs and raw data for accuracy
  • Ensure study document accountability
  • Provide clinical updates to bioanalytical teams
  • Address QC/QA observations
  • Conduct informed consent and screening
  • Prepare/review SOPs and train staff
  • Support pharmacy activities as needed
  • Perform delegated tasks from management

Benefits/Perks

  • Competitive salary package
  • Immediate joining opportunities
  • Professional growth in clinical research
  • Exposure to global regulatory standards
  • Training and skill development programs
  • Collaborative, quality-focused work culture
  • Contribution to innovative drug development

How to Apply

Interested candidates should email their updated CV to careers@synergenbio.com. Mention “CRA Application” in the subject line. Immediate joiners are preferred.

Verified Post

Verification: To confirm the legitimacy of this posting, you can view the original announcement on the Synergen Bio LinkedIn page.

Synergen Bio Hiring Clinical Research Associate (CRA) – Clinical Trials & BA/BE Jobs in Pune

For more clinical research and pharma opportunities, visit Pharma Recruiter. Start your CRA career in a dynamic CRO—apply today!

Why You Should Join

Synergen Bio offers an exciting environment for clinical research professionals in Pune’s growing pharma ecosystem. As a scientifically-driven CRO, it provides exposure to comprehensive BA/BE and clinical trial services.

Employees enjoy opportunities for training, regulatory expertise, and contributing to high-quality drug development. With a focus on innovation and compliance, Synergen Bio ensures career stability and professional recognition.

FAQs

What experience is required for the CRA role at Synergen Bio?

1-2+ years in clinical research, preferably BA/BE studies, with knowledge of regulatory guidelines.

Where is the Clinical Research Associate job located?

Shivajinagar, Wakadewadi, Pune (on-site role).

What key activities will I handle as a CRA?

Study execution, document preparation/review, informed consent, screening, SOP management, and compliance tasks.

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