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Role Description The Clinical Project Assistant role at Bionergyx Private Limited is a full-time, on-site position based in the Mumbai Metropolitan Region. The role involves supporting global clinical project teams with day-to-day coordination activities, including organizing meetings, maintaining project documentation, and tracking timelines and deliverables. Responsibilities include assisting with study start-up activities, supporting site communication, and helping ensure that clinical operations follow relevant protocols and regulatory requirements. The Clinical Project Assistant will collect and organize research data, prepare reports and status updates, and collaborate with cross-functional teams to facilitate smooth project execution. The role also includes maintaining accurate records, updating project management tools, and providing administrative support to project leads and clinical staff.
Qualifications
- Candidates should possess strong Communication skills, including clear written and verbal communication and the ability to interact professionally with internal teams and external stakeholders.
- Candidates should possess solid Research skills, such as information gathering, data organization, and basic data interpretation relevant to clinical projects.
- Candidates should possess Project Management skills, including task prioritization, timeline tracking, documentation management, and attention to detail.
- Candidates should possess Clinical Operations skills, with familiarity in site coordination, study documentation, and compliance with clinical procedures and guidelines.
- Candidates should possess Clinical Research Experience, preferably through internships, academic projects, or prior roles in clinical trial support or healthcare research.
- Relevant qualifications may include a bachelor’s degree in life sciences, pharmacy, nursing, public health, or a related field.
- Additional beneficial skills include proficiency in MS Office or similar productivity tools, basic understanding of regulatory and ethical standards in clinical research, and the ability to work collaboratively in a structured environment.
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