About IQVIA: IQVIA is a global leader in providing advanced analytics, technology solutions, and clinical research services to the life sciences industry. Our mission is to push the boundaries of human science and data science, creating a healthier world through innovative solutions and impactful research. With a strong focus on integrity and excellence, IQVIA is at the forefront of driving positive change in healthcare. Job Overview of Trainee Medical Writer: As a Fresher Trainee Medical Writer at IQVIA, you will be part of a structured program designed to enhance your skills and knowledge in medical writing. Under senior supervision, you will support medical writing deliverables and focus on specific tasks to gain valuable experience in the field. This role offers a platform to stay updated with current medical and technical writing knowledge, including Good Clinical Practice (GCP) standards, and contribute to meaningful projects. Essential Functions:
- Gain hands-on experience in medical writing tasks such as writing patient narratives and drafting assigned documents.
- Manage day-to-day workload, track timelines, and implement review comments with senior guidance.
- Interact with internal clients and stay informed about developments in drug development and medical writing.
- Ensure compliance with customer requirements and IQVIA Standard Operating Procedures (SOPs).
- B Pharmacy, M Pharmacy, Pharma D , Bachelor's Degree Bachelor's Degree in life sciences related discipline or related field Req
- Master's Degree Master's Degree in life sciences related discipline or related field Pref
- Ph.D. Ph.D. in life sciences related discipline or related field Pref
- This is an entry level trainee position and as such education, skills, and potential are more important than formal work experience. However, experience and strong ability in scientific writing in English gained from academic studies or work experience is essential.
- Awareness of drug development, medical writing, and associated regulations. Good understanding of statistical principles and of medical terminology across a range of therapeutic areas.
- Familiarity with the structural and content requirements of clinical study reports, protocols, and similar documents.
- Good understanding of common statistical methods used in clinical trials and/or interpretation of their results.
- Ability to integrate, interpret, and summarize data from a variety of sources in a clear and concise manner.
- Excellent written and oral communication skills including grammatical/technical writing skills.
- Excellent attention to detail and accuracy.
- Communicates clearly, effectively and confidently with others.
- Demonstrated abilities in collaboration with others and independent thought.
- Demonstrates confidence and maturity in most routine medical writing situations.Demonstrates good judgement in requesting input from senior staff. Ability to establish and maintain effective working relationships with coworkers, managers and customers.
- Ability to effectively manage multiple tasks and projects.
- Must be computer literate.