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Clinical Trial Incharge / Site Manager (MBBS/M-Pharma)

Clinical Trial Incharge / Site Manager (MBBS/M-Pharma)

REGUL SOLUTIONS

15 years

12 - 180 Lacs

hyderabad telangana india

Posted:5 days ago| Platform:

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Skills Required

research monitoring oncology compliance gcp recruitment data documentation audits logistics pharmacology management schedule communication coordination leadership

Work Mode

On-site

Job Type

Full Time

Job Description

Job Title

Clinical Trial Incharge / Site Manager – Research Department

Location:

American Cancer Institute & Hospital, Hyderabad

Role Summary

Responsible for coordinating, managing, and monitoring clinical trials in the oncology research department, ensuring compliance with GCP, ICMR, and regulatory guidelines.

Key Responsibilities

Oversee day-to-day conduct of clinical trials.
Coordinate with investigators, CROs, and sponsors.
Ensure protocol adherence, regulatory submissions, and IEC approvals.
Supervise patient recruitment, consent, and data collection.
Maintain documentation, drug accountability, and trial master files.
Prepare for audits and monitoring visits.
Manage trial budgets and site logistics.
Train and guide research staff on GCP and SOPs.

Qualifications

MBBS / M.Pharm / M.Sc (Life Sciences / Clinical Research) / MD Pharmacology.
10–15 years of experience in clinical trial management, preferably oncology.

Skills

Strong knowledge of GCP, ICMR, and Schedule Y.
Excellent communication & coordination skills.
Proficient in MS Office and EDC/CTMS systems.
Detail-oriented with leadership ability.

Type

Full-Time | On-Site | Salary as per institutional normsSkills: research,cancer,clinical trials,trials,oncology

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Clinical Trial Incharge / Site Manager (MBBS/M-Pharma)