IQVIA Walk In Interview 2023.IQVIA Notification full details below..Interested and eligible candidates can attend interview on scheduled time and venue.Innovative emerging biopharma and biotech companies are driving the drug development pipeline; competition for funding and resources is fierce. IQVIA delivers flexible clinical development solutions designed for the specific needs of biotech companies.
- Post Name: Medical Writing Trainee – India
- Educational Qualification :Bachelor’s Degree (BAMS, BHMS, BDS) Life science-related discipline or related field/Advanced Degree (MPharm, MSc or PhD) Life science-related discipline or related field
Job Description: Greeting from IQVIA Ltd !!!!
Important Details :
- Location: Thane, Maharashtra
- Post of date:20/04/2023
- Selection Process: The selection will be on the basis of Interview.
- Mode of Interview: Face To Face Interview
- Interview Rounds of Interview: HR
Job Family Description
Writes, reviews, and coordinates preparation of clinical trial documentation in line with client specifications and industry practices.
Prepares, or contributes to the preparation of clinical and regulatory documents for external clients, for investigational drugs, biologicals, or medical devices.
Collaborates with internal and external experts and specialists and maintains expertise on developments in a particular field of focus.
Job Profile Summary
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.
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.
MINIMUM REQUIRED EDUCATION AND EXPERIENCE
To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.
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.