Hiring For Clinical Research Director

Talent Zone Consultant; Kolkata District; On-site; INR 4,200,000 - 6,200,000; Full time

Job summary

Talent Zone Consultant is seeking a seasoned Clinical Research Manager in Kolkata to lead clinical research programs and oversee trials, ensuring regulatory compliance with ICH-GCP, CDSCO, and related guidelines. The position requires 15-18 years of experience and advanced qualifications.

You will design studies, manage teams and vendors, monitor data quality and patient safety, and drive strategy, quality standards, and efficiency within a pharma setting in India.

Qualifications

• PhD/MD/PharmD or Master’s in Clinical Research or Life Sciences.
• 15+ years of relevant clinical research experience.

Responsibilities

• Lead and oversee clinical research studies and trial operations.
• Design and review clinical study protocols and research plans.
• Ensure compliance with ICH-GCP, CDSCO, and regulatory guidelines.
• Manage clinical trial teams, investigators, CROs, and research partners.
• Monitor trial progress, data quality, and patient safety.
• Oversee clinical documentation, audits, and regulatory submissions.
• Drive research strategy, quality standards, and operational efficiency.

Skills

Clinical Research

Clinical Trials

ICH-GCP

Clinical Study Management

Protocol Development

Regulatory Compliance

CDSCO

Clinical Data Management

Pharmacovigilance

Research Operations

Education

PhD / MD / PharmD / Master's in Clinical Research

Job description

Job openings for Clinical Research Manager in Kolkata

Hiring: Clinical Research Director
Location: Kolkata
Experience: 15-18 Years
Industry: Healthcare / Pharmaceuticals / Clinical Research
Talent Zone Consultant is hiring an experienced Clinical Research professional to lead clinical research programs, oversee clinical trials, ensure regulatory compliance, and drive research excellence.

Key Responsibilities

• Lead and oversee clinical research studies and trial operations.
• Design and review clinical study protocols and research plans.
• Ensure compliance with ICH-GCP, CDSCO, and applicable regulatory guidelines.
• Manage clinical trial teams, investigators, CROs, and research partners.
• Monitor trial progress, data quality, and patient safety.
• Oversee clinical documentation, audits, and regulatory submissions.
• Drive research strategy, quality standards, and operational efficiency.

Key Skills

• Clinical Research
• Clinical Trials
• ICH-GCP
• Clinical Study Management
• Protocol Development
• Regulatory Compliance
• CDSCO
• Clinical Data Management
• Pharmacovigilance
• Research Operations

Qualification

• PhD / MD / PharmD / Master's degree in Clinical Research, Pharmacy, Life Sciences, or a related discipline.

Education Requirements: Bachelor's or Master's degree in Pharmacy, Medicine, Biotechnology, Life Sciences, or a related field. Advanced research qualifications preferred.

Find Recruiters

Experience 15 - 18 Years

Salary Not Disclosed

Industry Pharma / R&D / Biotech

Qualification

Key Skills Clinical Research Clinical Trials Ich-Gcp Clinical Study Management Protocol Development Regulatory Compliance Cdsco Clinical Data Management Pharmacovigilance Research Operations