Himalaya Drug Company Medical Writing Job – Apply Online
Himalaya drug company Pharma Jobs.Pharma jobs. RA post at Himalaya. pharma jobs 2021 M Pharma jobs at Himalaya. Job Opportunity for pharmacy candidates with the firm Himalaya. Check out all the details on the same below:
Job Title: Lead Scientist: Medical Writing
Location: Bengaluru
Experience: From 5 to 8 years of experience
Eligibility Criteria:
- M Pharm/ MSc/ Pharm D/ BDS/ PhD (Pharmacology) or degree in alternative medicine (BAMS/ BHMS) with 5 years experience in Medical writing (related to Clinical Trials Document & Publications).
- Hands-on experience in literature search, targeted literature review, preparation of the scientific document, disease or drug-related literature based on data available from publications, clinical trials.
- Experience in preparation of scientific abstracts, publication would be preferred
- Desirable to have a thorough knowledge of clinical trial concepts including ICH-GCP, CFR, and applicable regulatory guidelines (DCGI, USFDA, MHRA)
Desired Candidate Profile
- Medical writing skills, including grammatical, editorial, and proofreading skills.
- Good knowledge of English grammar with a familiarity of writing clinical trial documents
Familiarity with the principles of clinical research - Knowledge of global, regional, national, and other document development guidelines
The comfort of searching the scientific information available on open resources. - Ability to communicate scientific or medical information in a clear and concise manner
- Must be aware of current industry practices and regulatory requirements.
- Must keep abreast of current literature, emerging science, technological developments, and medical trends.
Roles and Responsibilities
- Responsible for preparation and review of clinical trial documents (Investigators
- Brochure, Protocol, ICD) in accordance with documented guidelines, SOPs within stipulated timelines.
- Effectively accomplish the medical writing activities & build expertise across the different document types assigned.
- Interpretation of clinical data and other related information in a most acceptable quality document (Interim Report or Clinical Study Report)
- Co-ordinate and maintain an effective relationship with Scientific Strategy and Medical writing team and Clinical Operations study team to provide high-quality Clinical trial documents.
- Provide scientific feedback on the essential documents related to the conduct of the clinical trial.
- Write scientific abstracts, publications, related to clinical studies.
- Provide scientific inputs on Healthcare websites, health magazines, etc.
- Work closely with a multidisciplinary group of experts to translate the study data and results into presentations, reports, regulatory documents, scientific journal manuscripts, and abstracts for publication.
- Should conduct comprehensive literature searches to enhance background understanding and evaluate and analyze the information.
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