Sandoz Clinical DD & BD Manager Jobs

Sandoz Hiring Clinical DD & BD Manager in Telangana

Sandoz has announced a new hiring opportunity for the position of Clinical DD & BD Manager under its Research & Development division in Telangana. The company is seeking experienced professionals with expertise in clinical development, due diligence, business development support, regulatory strategy, and pharmaceutical research. This opportunity is ideal for candidates looking to build careers in clinical development, licensing evaluation, regulatory affairs, and pharmaceutical business strategy.

Professionals searching for clinical development jobs in Hyderabad, clinical research manager vacancies, pharmaceutical business development careers, regulatory affairs jobs, due diligence specialist roles, and drug development opportunities may find this position highly relevant.

Company Overview

Sandoz is a global leader in generic and biosimilar medicines, committed to improving patient access to high-quality and affordable healthcare solutions. The company operates across multiple international markets and focuses on research-driven development, regulatory excellence, and strategic partnerships that support healthcare innovation.

With a strong presence in pharmaceutical development, regulatory science, and clinical research, Sandoz continues to expand its capabilities through strategic collaborations and licensing opportunities. The company offers professionals exposure to global clinical development programs, regulatory pathways, and scientific evaluation processes.

Job Role & Responsibilities

Clinical DD & BD Manager Responsibilities

The selected candidate will support clinical due diligence and business development activities while working closely with regulatory, clinical development, and licensing teams.

Key responsibilities include:

• Evaluating clinical development programs and dossiers from partner companies
• Reviewing clinical, bioanalytical, in-vitro, and dissolution study data
• Preparing dossier assessment reports for business development and regulatory teams
• Identifying project risks and recommending mitigation strategies
• Providing scientific and regulatory guidance to partner organizations
• Supporting business development teams during licensing evaluations
• Assisting budget planning and contract negotiation activities
• Collaborating with regulatory teams on deficiency letter responses
• Developing clinical strategies for assigned markets and countries
• Monitoring ongoing and planned clinical development activities
• Providing scientific support for clinical studies related to business development products
• Collaborating with global clinical development teams and strategic initiatives
• Supporting continuous improvement and professional development activities

Skills Required

Candidates should possess:

• Clinical development expertise
• Regulatory affairs knowledge
• Clinical due diligence experience
• Scientific data evaluation skills
• Risk assessment and mitigation capabilities
• Pharmaceutical licensing and business development understanding
• Clinical study strategy development skills
• Communication and stakeholder management abilities
• Regulatory documentation review experience
• Strong analytical and problem-solving skills
• Microsoft Office proficiency

Eligibility / Qualifications

Educational Qualification

Candidates with science and healthcare educational backgrounds are eligible.

Relevant educational qualifications include:

B.Pharm, M.Pharm, Pharm.D, MBBS, BSc Life Sciences, MSc Life Sciences, Biotechnology, Pharmacology, Clinical Research, Biomedical Sciences, Pharmaceutical Sciences.

Experience Requirement

• Minimum 3 years of experience in clinical development or related fields
• Experience in clinical research, regulatory affairs, or pharmaceutical development preferred
• Business development or licensing evaluation exposure preferred
• Clinical strategy and dossier review experience preferred

These openings are suitable for:

• Clinical Development Managers
• Clinical Research Professionals
• Regulatory Affairs Specialists
• Due Diligence Professionals
• Pharmaceutical Business Development Associates
• Clinical Strategy Professionals
• Drug Development Scientists

Location & Salary

Location

Telangana, India

Estimated Salary

₹12 LPA – ₹22 LPA approximately

Salary may vary depending on clinical development expertise, regulatory knowledge, due diligence experience, and pharmaceutical industry exposure.

Application Process

Interested candidates can apply through the official Sandoz careers portal.

Apply Online

https://www.sandoz.com/careers/career-search/job-details/REQ-10028485/clinical-dd-bd-manager/

Job ID

REQ-10028485

Department

Research & Development

Business Unit

Development

Frequently Asked Questions (FAQs)

1. What role is Sandoz hiring for?

Sandoz is hiring for the position of Clinical DD & BD Manager.

2. Which qualifications are eligible for this opportunity?

Candidates with Pharmacy, Medicine, Life Sciences, Biotechnology, Pharmacology, and related science qualifications can apply.

3. What experience is required for this role?

A minimum of 3 years of experience in clinical development or related fields is required.

4. What are the key responsibilities of a Clinical DD & BD Manager?

The role involves clinical due diligence, dossier review, regulatory support, business development collaboration, clinical strategy development, and risk assessment.

5. What is the estimated salary for this position?

The expected salary range is approximately ₹12 LPA to ₹22 LPA depending on experience and expertise.

6. Where is this position located?

The role is based in Telangana, India.

Summary Table

Tagged as: Pharma Jobs in Hyderabad