1. Scientific and medical documentation:
a. Assist in drafting, reviewing, and maintaining scientific documents, including research reports, clinical data, and patient outcomes.
b. Support in the preparation of regulatory submissions, ensuring compliance with ICH-GCP, GLP, and GMP standards.
c. Work with the R&D team to document findings from animal studies, lab protocols, and clinical research.
2. Lab and research documentation:
a. Collaborate with teams from the GMP lab and R&D center to maintain up-to-date lab records, research protocols, and experimental results.
b. Contribute to the development and maintenance of Standard Operating Procedures (SOPs) for lab and research activities.
3. Clinical and regulatory support:
a. Compile and organize clinical data and patient-related outcomes for research studies.
b. Assist in the submission of documentation for regulatory bodies such as DCGI, CDSCO, and other relevant authorities.
c. Ensure that all documentation complies with ethical and regulatory standards.
4. Communication and coordination:
a. Coordinate communication between the Founder's Office, research teams, and external stakeholders.
b. Organize and participate in meetings, reviews, and presentations related to ongoing research and documentation.
c. Collaborate with other departments to ensure proper alignment on research projects and data management.
5. Documentation and report writing:
a. Draft, edit, and review scientific reports, publications, and presentations related to lab and clinical research.
b. Assist the CSO in the preparation of technical papers, grant applications, and other formal documents.
6. Data analysis and presentation:
a. Organize and interpret clinical and experimental data, presenting it in charts, graphs, and reports.
b. Support data analysis related to patient outcomes and clinical trial results.
7. Problem-solving and proactive support:
a. Confidently address challenges as they arise and propose effective solutions for scientific and operational issues.
b. Maintain a problem-solving mindset and contribute to improving processes within the research and documentation workflow.
Regrow is the 1st company in India to offer cell therapy in orthopedic products, and was established in the year 2009 to introduce cutting edge technology platform for regenerative medicine in India. The company headquarters is in Mumbai, India and has the best in class cell processing and cryopreservation facilities with strong R&D capabilities at Lonavala.