Palamur Biosciences Study Director – Medical Device Division

Life Sciences Study Director Vacancies – Medical Devices

Study Director vacancies for Life Sciences & Veterinary postgraduates with GLP experience in medical device research. Apply now.

Palamur Bio is expanding its Medical Device Division (MRIDA) and invites applications from experienced Study Directors who are passionate about preclinical research, medical device safety, and translational science. This role offers a rare opportunity to work on advanced interventional and large-animal studies within a globally aligned GLP research environment.

Company Overview

Palamur Biosciences is a specialized preclinical research organization focused on non-clinical safety, efficacy, and performance evaluation of medical devices and biomedical innovations. Through its Medical Device Research Infrastructure Development Area (MRIDA), Palamur Bio supports regulated studies aligned with global standards, helping innovators bring safer and more effective medical devices to patients.

With state-of-the-art large-animal research facilities, interventional laboratories, and strong GLP systems, Palamur Bio has positioned itself as a trusted partner for medical device developers, CROs, and healthcare innovators in India and internationally.

Job Role & Responsibilities

Study Director – Medical Device Division

The Study Director will have overall scientific and regulatory responsibility for the design, execution, monitoring, and reporting of GLP-compliant medical device studies.

Key responsibilities include:

• Acting as the single point of study control in accordance with GLP requirements
• Designing and approving study protocols for medical device safety and performance studies
• Overseeing conduct of large-animal and interventional research studies
• Ensuring compliance with GLP, SOPs, and applicable regulatory guidelines
• Coordinating with veterinarians, surgeons, pathologists, QA, and technical teams
• Monitoring study progress, deviations, and corrective actions
• Reviewing, approving, and signing final study reports
• Ensuring data integrity, documentation accuracy, and archival compliance
• Supporting sponsor interactions, audits, and regulatory inspections

This position directly contributes to the safety evaluation of innovative medical devices used in critical healthcare interventions.

Eligibility / Qualifications

Educational Background

Candidates must hold a postgraduate degree in one of the following disciplines:

Veterinary Science, Life Sciences, Biomedical Sciences, Pharmacology, Toxicology, or related fields

Experience Requirements

• 2 to 3 years of proven experience as a Study Director in a GLP-compliant environment
• Prior experience in medical device studies is strongly preferred
• Exposure to large-animal research and interventional procedures is an advantage

Key Skills & Competencies

• Strong understanding of GLP principles and regulatory expectations
• Experience in protocol writing, study oversight, and report finalization
• Ability to manage cross-functional scientific teams
• Excellent scientific writing, documentation, and communication skills
• Commitment to ethical research and animal welfare standards

Location & Career Growth

Job Location: Palamur Bio – Medical Device Division (MRIDA), Telangana

Palamur Bio offers long-term career growth for professionals seeking leadership roles in preclinical research, regulatory science, and medical device development. Compensation will be competitive and aligned with industry standards based on experience and expertise.

Application Process

Interested candidates are requested to email their updated CV to:

dcsharma@palamurbio.com

Candidates are encouraged to mention their Study Director experience, GLP exposure, and medical device background in the application.

Why Choose a Career in Medical Device Research?

Medical devices play a critical role in modern healthcare, from life-saving implants to minimally invasive interventional tools. Study Directors ensure that these devices meet safety and performance expectations before reaching patients. This role offers high professional impact, regulatory visibility, and long-term career stability.

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Frequently Asked Questions (FAQs)

Is Study Director experience mandatory?

Yes. Candidates must have prior experience as a Study Director in a GLP-compliant environment.

Are pharmaceutical-only backgrounds acceptable?

Candidates with strong GLP experience may apply, but medical device study exposure is preferred.

What type of studies will be handled?

The role involves medical device safety, performance, and interventional studies, often using large-animal models.

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Company	Palamur Biosciences
Vacancies	Study Director – Medical Device Division
Required Education	Veterinary Science, Life Sciences, Biomedical Sciences (Postgraduate)
Experience	2–3 Years