Clinical Pharmacist

Alexander Rd, Kummari Guda, Shivaji Nagar, Secunderabad, Telangana 500003; Hyderabad; On-site; INR 400,000 - 540,000; Full time

Job summary

Unknown Company in Hyderabad is seeking a Clinical Trial Assistant to support planning, coordination, and monitoring of clinical research studies. You will collaborate with investigators, study participants, and clinical teams to ensure proper record keeping and documentation.

The role involves assisting with data collection, maintaining essential study documents, coordinating with Ethics Committees, and supporting audits to ensure protocol compliance.

Qualifications

• Basic understanding of clinical trial processes and documentation.
• Good communication and interpersonal skills.
• Good documentation and analytical skills.
• Ability to work effectively with doctors, patients, and clinical teams.
• Basic knowledge of MS Office, especially Word and Excel.

Responsibilities

• Assist in planning, coordinating, and monitoring clinical research studies.
• Coordinate with investigators, study participants, and clinical teams.
• Maintain clinical trial documentation and ensure proper record keeping.
• Support patient recruitment, screening, and follow-up activities.
• Ensure clinical studies are conducted
• Assist with collection, review, and verification of clinical data.
• Prepare and maintain essential study documents and reports.
• Coordinate with the Ethics Committee and other study-related stakeholders.
• Monitor study progress and identify/report deviations or issues.
• Support audits and regulatory inspections when required.
• Maintain confidentiality and ensure compliance with study protocols.

Skills

Clinical trials

Communication skills

Documentation

Interpersonal skills

MS Office

Tools

MS Office (Word & Excel)

Job description

• Assist in planning, coordinating, and monitoring clinical research studies.
• Coordinate with investigators, study participants, and clinical teams.
• Maintain clinical trial documentation and ensure proper record keeping.
• Support patient recruitment, screening, and follow-up activities.
• Ensure clinical studies are conducted
• Assist with collection, review, and verification of clinical data.
• Prepare and maintain essential study documents and reports.
• Coordinate with the Ethics Committee and other study-related stakeholders.
• Monitor study progress and identify/report deviations or issues.
• Support audits and regulatory inspections when required.
• Maintain confidentiality and ensure compliance with study protocols.

Required Skills

• Basic understanding of clinical trial processes and documentation.
• Good communication and interpersonal skills.
• Good documentation and analytical skills.
• Ability to work effectively with doctors, patients, and clinical teams.
• Basic knowledge of MS Office, especially Word and Excel.