Clinical Pharmacist

• 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.