Clinical Trial Assistant
Company: Ishwar institute of health care
- Location: Aurangabad, India
- Seniority: Entry level
- Employment type: Full-time
- Posted: 13 days ago
- Offer language: English
Job description
Company Description Ishwar Institute of Health Care is a healthcare organization committed to delivering quality clinical services and supporting medical research and education. The institute focuses on evidence-based practices and patient-centered care, providing an environment where clinical teams and research professionals collaborate closely. Located in Aurangabad, Ishwar Institute of Health Care aims to improve health outcomes through structured clinical programs and ethical research. Team members benefit from opportunities to develop their skills while contributing to the advancement of healthcare in the region.
Role Description The Clinical Trial Assistant is a full-time, on-site role based in Aurangabad, supporting the planning, conduct, and documentation of clinical trials. The role involves maintaining and organizing the Trial Master File (TMF), assisting with study start-up activities, and ensuring that essential documents are complete, accurate, and up to date. The Clinical Trial Assistant will help coordinate site communications, schedule meetings and visits, and track trial-related timelines and milestones. Daily responsibilities include supporting clinical operations teams with data entry, filing, and regulatory documentation, as well as assisting with preparation of study materials and reports. The role also requires close collaboration with investigators, study coordinators, and other stakeholders to facilitate smooth trial execution and adherence to protocols and compliance standards.
Qualifications
- Candidates should possess strong Communication skills for effective interaction with investigators, site staff, and internal clinical operations teams.
- Candidates should possess Trial Master File (TMF) management skills to organize, maintain, and audit essential documents for clinical studies.
- Candidates should possess Research skills to support literature review, data collection, and basic analysis in alignment with study protocols.
- Candidates should possess Clinical Operations and Clinical Trials knowledge to understand study workflows, regulatory requirements, and Good Clinical Practice (GCP) guidelines.
- Relevant qualifications such as a bachelor’s degree in life sciences, pharmacy, nursing, or a related healthcare field.
- Strong attention to detail, organizational skills, and proficiency with office productivity software and electronic documentation systems.
- Ability to work collaboratively in a multidisciplinary environment and manage multiple tasks with appropriate prioritization.
- Prior experience or internship in clinical research or hospital-based clinical operations is an advantage.
