Job Title

CONGRATULATIONS! For the 1st time in your career as a researcher, this role will NOT: 1) Ask you to GHOST WRITE research papers. Your name will be on the papers you write. This role will 1) Rate you on the quality of the papers you write and what impact factor journals you get them published! Position: Manager, Medical Writing & Research Affairs, TECCRO Job Type: Full-Time (On-Site) Location: Bandra Kurla Complex, Mumbai Qualifications: Educational Requirements: A PhD in Biological Sciences, Biotechnology, Life Sciences, or a closely related field is highly preferred. MBBS/ MDS/ MD will be an additional advantage Certifications or additional qualifications in Clinical Research or Medical Writing are an advantage. Experience: A minimum of 5-10 years of experience in medical writing or scientific publication, particularly within the clinical research, pharmaceutical, or CRO industry. Proven track record of at least 10 peer-reviewed publications in PubMed-indexed journals, with preference for research in medical aesthetics, clinical trials, or related fields. Demonstrated expertise in the preparation of clinical study reports, research articles, regulatory documents, and scientific content. Experience working in or with clinical research teams and understanding the nuances of clinical trial documentation. Company Overview: TECCRO (The Esthetic Clinics Clinical Research Organisation) operates as a premier Clinical Research Organisation (CRO) specializing in aesthetics, under the umbrella of The Esthetic Clinics and QR678. With a focus on clinical research services spanning product development, medical writing, and clinical trials in cosmetic and reconstructive surgeries, skincare, and therapies for various skin conditions, TECCRO plays a key role in driving scientific and technological innovation in the aesthetics industry. Role Overview: TECCRO is seeking a highly skilled and experienced Medical Writer to join the team. This role will focus on preparing high-quality scientific documents, including clinical study reports, research papers, regulatory submissions, and publications for medical journals. The ideal candidate will bring an in-depth understanding of clinical research, a strong background in scientific writing, and expertise in academic publication. A PhD and a proven record of publications in prestigious, peer-reviewed journals are essential for this role. Key Responsibilities: Scientific Writing & Publication: Write, review, and edit high-quality scientific documents including clinical study reports, research papers, regulatory submissions, and academic publications. Ensure manuscripts meet publication standards for major medical journals and are aligned with the latest scientific research and TECCRO’s clinical objectives. Collaborate closely with clinical and research teams to produce content that adheres to regulatory requirements and scientific standards. Medical Research & Literature Review: Conduct thorough literature reviews and contribute to the design of clinical trials by writing study protocols and other essential documents. Stay updated with current scientific and clinical advancements in the fields of medical aesthetics, skincare, and clinical trials. Provide input into research design, methodologies, and statistical analysis to ensure clarity and accuracy in the documentation. Collaboration with Cross-Functional Teams: Work closely with internal teams including clinical researchers, data managers, and regulatory affairs to ensure the alignment of documents with clinical objectives and regulatory standards. Support the creation of regulatory documents such as INDs, NDAs, CTAs, and clinical trial reports. Academic and Research Publications: Write and submit research papers to top-tier, PubMed-indexed journals, aiming for publication in highly reputable scientific outlets. Coordinate with external authors, principal investigators, and researchers to support the publication process. Present research findings at conferences, webinars, and academic meetings, contributing to TECCRO’s visibility within the global research community. Regulatory Affairs Support: Assist in the preparation of regulatory submissions, ensuring that scientific documents align with required formats and regulatory guidelines. Ensure the quality and compliance of all written materials with the standards set by ethical guidelines, GCP, ICH, and relevant regulatory authorities. Business Development Support: Provide expertise in medical writing to support business development efforts, including proposal creation and client communication. Participate in business development meetings to provide scientific content expertise and engage in discussions around research capabilities. Skills & Competencies: Exceptional writing, editing, and proofreading skills with a meticulous attention to detail. Strong understanding of clinical research methodologies, regulatory guidelines (FDA, EMA), Good Clinical Practices (GCP), and ICH guidelines. Ability to distill complex scientific concepts into clear, concise, and compelling content for both scientific and non-scientific audiences. Proficient in using writing and reference management software (e.g., EndNote, Microsoft Word, LaTeX). Excellent collaboration skills and the ability to work effectively across cross-functional teams. A proactive attitude with the ability to handle multiple projects under tight deadlines. Personal Attributes: Detail-oriented with a strong commitment to scientific accuracy and excellence. Analytical mindset with the ability to interpret and present clinical data effectively. Highly motivated and results-driven, with a passion for advancing clinical research and medical science. Ability to work independently and collaboratively in a dynamic, fast-paced environment. Benefits: Competitive salary with performance-based incentives. Opportunities for professional development, certifications, and career growth. Supportive and collaborative work environment focused on research excellence and innovation in clinical trials. Access to cutting-edge clinical research resources and participation in groundbreaking aesthetic medical projects. This role offers an exciting opportunity to contribute to the advancement of clinical research and academic publications within the growing field of medical aesthetics. If you are a skilled medical writer with a passion for science and research, we would love to hear from you. Salary - 6 to 18 L per annum, depending on competence and strength of current CV