Veeda Clinical Research Limited is a leading, independent, full-service Clinical Research Organization (CRO) in India. Known for its commitment to delivering high-quality research solutions, Veeda specializes in Biopharmaceutical studies, Medical Affairs, and Pharmacovigilance. With a strong foundation in clinical trial management, Veeda Clinical Research has successfully conducted Phase I-IV studies, making a significant impact on healthcare innovation.
Job Openings at Veeda Clinical Research
1. Medical Writer – Biopharmaceutical & Project Management
Location: Ahmedabad
Experience: 1 to 3 years (Internship experience also considered)
Education: M.Pharm or equivalent
Key Responsibilities:
- Collaborate with cross-functional teams (Project Managers, Principal Investigators, Clinical Investigators, Bioanalytical teams, and Statisticians) for protocol preparation.
- Prepare and coordinate translations of Informed Consent Documents (ICD) as necessary.
- Draft Case Report Forms (CRFs) and other supporting study documents.
- Prepare essential documents required for regulatory submissions.
- Incorporate feedback and ensure quality control for all study-related documents.
- Conduct literature searches to gather and organize data for document preparation.
Qualifications and Skills:
- M.Pharm or equivalent degree.
- 1 to 4 years of relevant experience in medical writing or related fields.
- Internship experience will be considered.
- Strong attention to detail and ability to meet deadlines.
- Excellent communication and documentation skills.
How to Apply: Share your updated resume via email to Vaibhav.D3662@veedacr.com or connect through WhatsApp at 6355085964 (WhatsApp only).
2. Regulatory Scientific Writer
Location: Ahmedabad
Department: Medical Affairs and Pharmacovigilance (MPD)
Experience: 2 to 5 years
Education: M.Pharm or B.Pharm
Key Responsibilities:
- Prepare and review study-specific documents such as Protocols, Informed Consent Documents (ICD), Synopsis, and patient diary cards.
- Prepare and review Investigator Brochures.
- Conduct trial feasibility assessments (preliminary and detailed) for patient-based clinical studies alongside the medical team.
- Perform reference literature searches to support assigned projects.
- Provide protocol training to Monitors and site teams as needed.
- Prepare and review Clinical Study Reports (CSRs) for phase trials conducted by the Clinical Operations Department, ensuring compliance with regulatory requirements and project timelines.
Qualifications and Skills:
- M.Pharm or B.Pharm (preferably in Life Sciences, Pharmacy, or a related field).
- 2 to 5 years of experience in regulatory writing or related areas.
- Strong analytical and research skills.
- Ability to manage multiple projects with attention to detail.
- Excellent verbal and written communication skills.
How to Apply: Share your updated resume via email to Vaibhav.D3662@veedacr.com or connect through WhatsApp at 6359600877 (WhatsApp only).
