Shri Chaitanya Health And Care Trust is a leading healthcare organization seeking a highly skilled Medical Writer/Clinical Research Associate to join their dynamic team. With a focus on delivering exceptional patient care and conducting cutting-edge research, they are committed to advancing the field of medicine.
Job Description:
We are currently seeking a Medical Writer/Clinical Research Associate with a strong background in medical writing and a passion for clinical research. The successful candidate will be responsible for drafting and editing clinical study protocols and informed consent forms, as well as preparing manuscripts for publication. If you are a detail-oriented professional with excellent writing skills and a keen eye for quality, we encourage you to apply.
Key Responsibilities:
- Draft and edit clinical study protocols and informed consent forms, ensuring adherence to regulatory guidelines and industry standards.
- Prepare manuscripts for publication, including writing, editing, and formatting to ensure journal formatting and structure guidelines are met.
- Collaborate with cross-functional teams, including researchers, clinicians, and subject matter experts, to ensure the accuracy and quality of research outputs.
- Author and co-author publications, posters, and presentations, and participate in scientific meetings and conferences to stay up-to-date with the latest developments in medical research.
- Maintain accurate and detailed records of research activities, including study protocols, patient data, and research output tracking.
Must-Have Qualifications:
- A degree in Life Sciences, Pharmacy, or a related field (MBBS, MS, or Ph.D.).
- At least one original article published in a reputable medical journal.
- Proven experience in medical writing, including drafting clinical study protocols, informed consent forms, and research articles.
- Excellent written and verbal communication skills, with the ability to work effectively with cross-functional teams.
- Strong attention to detail and organizational skills, with the ability to meet deadlines and manage multiple projects simultaneously.
Nice-to-Have Qualifications:
- Experience in clinical trials and research studies, including regulatory affairs, good clinical practice (GCP), and institutional review board (IRB) compliance.
- Strong understanding of the pharmaceutical industry, including clinical research and development, regulatory affairs, and medical communications.
- Knowledge of journal formatting and structure guidelines, including American Medical Association (AMA) and International Committee of Medical Journal Editors (ICMJE).
What We Offer:
- Competitive salary and benefits package.
- Opportunities for professional growth and development.
- A dynamic and collaborative work environment.
- Flexible working hours and remote work options.
- Recognition and rewards for outstanding performance
