Hyderabad Telangana Pharmacy specialist Jobs – 70 Open Jobs Today

Documentation Specialist(Ethics Committee)
FORWARD LIFE PVT.LTD —Ameerpet, Hyderabad, Telangana
- ₹18,000 - ₹25,000 an hour
- Full-time
- Doctoral degree
- Microsoft Office
- Organisational skills
- Health insurance
Quick apply
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FORWARD LIFE PRIVATE LIMITED —Ameerpet, Hyderabad, Telangana
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Charles Schwab —Hyderabad, Telangana
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Genpact India Pvt. Ltd. —Hyderabad, Telangana
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Genpact India Pvt. Ltd. —Hyderabad, Telangana
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Optum —Hyderabad, Telangana
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Charles Schwab —Hyderabad, Telangana
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Sr Specialist, Software Engineering - BDSE
Charles Schwab —Hyderabad, Telangana
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Charles Schwab —Hyderabad, Telangana
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Documentation Specialist(Ethics Committee)

FORWARD LIFE PVT.LTD
Ameerpet, Hyderabad, Telangana

Quick apply

Job details

Permanent | Fresher | Full-time
₹18,000 - ₹25,000 an hour

Benefits

Provident Fund
Health insurance

Qualifications

Clinical research
Doctoral degree
Microsoft Office
Organisational skills
Pharmacy
Document management systems
Communication skills

Full job description

Job Title – Documentation Specialist(Ethics Committee)

Position: Clinical Research Documentation Specialist
Department: Ethics Committee (EC) Division
Reporting To: Head – Ethics Committee Division
Location: Hyderabad
Salary: ₹17,000 – ₹22,000 per month
Working Hours: Day Shift; may include rotational shifts
Qualification: Doctor of Pharmacy (Pharm. D) – Mandatory
Experience: Freshers or up to 1 year in clinical research or healthcare industry preferred
Age Limit: 21–30 years (recommended)
Employment Agreement: Must agree to a 2-year employment agreement
Shift Flexibility: Must be willing to work in rotational shifts
Industry: Clinical Research Organization (CRO)
Immediate Joiners: Preferred

Freshers / Experience Note:

Freshers or candidates with up to 1-year relevant experience are preferred.

Benefits:

Structured learning and growth opportunities in clinical research documentation.
Exposure to cross-functional activities across Ethics Committee and other divisions.
Collaborative, professional, and supportive work environment.

Role Overview

The Clinical Research Documentation Specialist supports the Head of the Ethics Committee (EC) Division by ensuring all clinical research documentation is accurate, compliant, and audit-ready. The role involves managing end-to-end documentation processes in alignment with ICH-GCP, institutional, and ethical standards and supporting cross-functional requirements across departments as needed.

Detailed Roles & Responsibilities

1. Regulatory Document Management

Coordinate Serious Adverse Event (SAE) reporting to regulatory authorities through the SUGAM portal within stipulated timelines, ensuring accuracy and completeness of documentation.
Support Ethics Committee registration, re-registration, and related submissions on SUGAM in accordance with CDSCO requirements. 2. Ethics Committee Coordination.
Support and facilitate regulatory audits/inspections by ensuring audit readiness, coordinating requirements, responding to auditor queries, and assisting in CAPA closure

2. Ethics Committee Coordination

Assist in preparing EC meeting agendas, presentations, and minutes.
Track approvals, re-approvals, and continuing reviews of studies.
Maintain precise documentation of EC decisions, communications, and correspondence.

3. Protocol & SOP Compliance

Ensure all activities adhere to SOPs, study protocols, and applicable regulatory standards.
Maintain documentation for audit and inspection readiness.

4. Communication & Liaison

Act as a liaison between clinical research teams and the Ethics Committee.
Coordinate with investigators, sponsors, and regulatory bodies for documentation and submissions.

5. Audit & Inspection Readiness

Support internal and external audits by providing organized and accurate documentation.
Implement Corrective and Preventive Actions (CAPA) in response to audit observations.

6. Training & Documentation Support

Conduct or assist with training sessions on documentation standards, GCP, and EC processes.
Contribute to drafting, reviewing, and updating SOPs related to EC documentation.

7. Archival & Record Management

Manage secure archival and retrieval of all EC and trial-related documents.
Ensure adherence to document retention and confidentiality policies.

Required Skills & Competencies

Strong understanding of ICH-GCP and clinical research regulations.
Excellent documentation and organizational skills.
Proficiency in MS Office and document management systems.
Strong attention to detail and accuracy.
Effective communication and coordination skills.
Ability to work cross-functionally and manage multiple priorities.
Knowledge of audit and inspection processes.
High level of confidentiality, professionalism, and ethical integrity.
Creative meeting context.
Awareness is important

Additional Notes

This is a cross-functional support role; the candidate may assist other divisions or departments as required.
The position contributes to ensuring all EC and clinical research documentation is audit-ready, compliant, and aligned with institutional goals.
Better performer and contributer will get the reward of Rs.1,00,000

Job Types: Full-time, Permanent, Fresher

Pay: ₹18,000.00 - ₹25,000.00 per hour

Benefits:

Health insurance
Provident Fund

Work Location: In person

Quick apply

Refine Your Search

pharmacy specialist jobs in hyderabad telangana

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