IQVIA is a leading global provider of advanced analytics, technology solutions and clinical research services to the life sciences industry. We believe in pushing the boundaries of human science and data science to make the biggest impact possible – to help our customers create a healthier world.
Name of Position: Medical Writing Trainee
Job Overview:
An entry level role within a structured program, supporting Medical Writing deliverables and focusing on specific tasks under senior supervision, while gaining experience, knowledge, and skills in Medical Writing.
Keeps abreast of current medical and/or technical writing/regulatory knowledge, including GCP, along with developments and advances in drug development/medical and/or technical writing.
Responsibilities:
- Gain knowledge, experience, and competence in specific Medical Writing tasks by supporting Medical Writing senior staff in managing client requests under supervision, focusing on tasks such as writing patient narratives.
- Manage day-to-day workload, track timelines, draft assigned documents to a high standard, and implement review comments and customer requests with senior guidance/review, keeping manager/senior staff abreast of progress on tasks and any potential problems.
- Interact with internal clients. May have some external interactions, mostly directed by senior staff.
- Keep abreast of current data, trends, medical and/or technical writing/regulatory knowledge, developments and advances in area of drug development/medical and/or technical writing.
- Comply with customer requirements and with IQVIA SOPs and standards.
Experience: 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.
Educational Qualification: Bachelor’s Degree (BAMS, BHMS, BDS); Life science-related discipline or related field; Advanced Degree (M. Pharm, MSc or PhD).
Additional Work Experience:
- 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.
Skills and Abilities:
- 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.
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