Palamur Bio is hiring Study Directors for its research operations. Candidates with a Master’s degree in Toxicology, Pharmacology, or related fields and minimum 2 years of GLP experience are encouraged to apply. Excellent opportunity for experienced professionals in pharma jobs and preclinical research.
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About the Company
Palamur Bio is a leading Contract Research Organization (CRO) specializing in partnering research and providing high-quality preclinical and toxicology services. The company is known for its scientific excellence, regulatory compliance, and state-of-the-art facilities.
With a strong focus on quality and innovation, Palamur Bio supports global pharmaceutical and biotech companies in advancing their drug development programs.
Job Details
- Company Name: Palamur Bio
- Position: Study Director
- Experience: Minimum 2 Years (GLP Experience Mandatory)
- Qualification: M.Sc / M.Pharm / Pharm.D in Toxicology, Pharmacology, or related field
- Location: (Not specified – likely Hyderabad / Telangana region)
- Work Type: On-site (Full-time)
Job Description
Palamur Bio is looking for experienced and detail-oriented Study Directors to lead preclinical toxicology and pharmacology studies. The role involves overseeing study design, execution, data interpretation, and regulatory compliance as per GLP standards.
Study Director
- Department: Toxicology / Preclinical Research
- Position: Study Director
- Experience: Minimum 2 Years GLP Experience
- Education/Qualification: M.Sc / M.Pharm / Pharm.D (Toxicology, Pharmacology, or related field)
Skills/Qualifications
- Minimum 2 years of hands-on GLP experience in toxicology or pharmacology studies
- Strong knowledge of OECD GLP guidelines and regulatory requirements
- Excellent written and verbal communication skills
- Ability to interpret scientific data and prepare study reports
- Leadership and project management capabilities
- Attention to detail and problem-solving skills
Key Responsibilities
- Design, plan, and oversee preclinical toxicology and pharmacology studies
- Ensure all studies are conducted in compliance with GLP regulations
- Monitor study progress and manage study teams
- Analyze data and prepare high-quality study reports
- Coordinate with sponsors and regulatory authorities
- Maintain accurate documentation and audit readiness
Benefits/Perks
- Work with a reputed and growing CRO
- Exposure to diverse preclinical research projects
- Professional growth in toxicology and regulatory science
- Collaborative and scientifically driven work culture
- Competitive compensation package
How to Apply
Interested candidates can send their updated CV or portfolio to: Email: jaish.jacob@palamurbio.com Phone / WhatsApp: +91 8130970158
For more pharma jobs, CRO, and toxicology opportunities across India, visit Pharma Recruiter.
Why You Should Join
Palamur Bio offers a dynamic environment for scientific professionals who want to make a meaningful impact in drug development. With a strong emphasis on quality research and regulatory excellence, the company provides excellent opportunities for career advancement in the preclinical research sector.
FAQs
What is the minimum experience required for Study Director at Palamur Bio?
Minimum 2 years of GLP experience is mandatory.
What qualifications are needed?
Master’s degree in Toxicology, Pharmacology, or related field (M.Sc., M.Pharm., Pharm.D.).
Is GLP experience mandatory?
Yes, minimum 2 years of GLP experience is required.
How can I apply for this position?
Send your CV to jaish.jacob@palamurbio.com or WhatsApp on +91 8130970158.
Where can I find more toxicology and preclinical research jobs?
Visit Pharma Recruiter for latest openings.
