Serilingampalli, Telangana, India
Posted: Jul 03, 2024
RemoteFull-time
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Skills Required
Medical Writing
expert
CRO
expert
Pharmaceutical
Proficient
Biotechnology
Proficient
Nice To Have skills
Job Description
About the job
The Senior Medical Writer will research, create, and edit all documents associated with clinical research. The Senior Medical Writer may operate as the project lead writer/submission coordinator and primary client contact to manage contributions of multiple writers working on related documents. The Senior Medical Writer also facilitates process improvement and technical mentoring/training and supports Medical Writing Services management during the sales process by providing client liaison and proposals input.

Minimum Qualification Requirements
  • Candidate must have 6+ have experience in regulatory medical writing. Experience in authoring protocols, clinical study reports, investigator’s brochures, informed consent forms, summary documents, etc.
  • Experience in multiple therapeutic areas, including but not limited to vaccines, immunology, autoimmune disorders, cardiovascular disorders, endocrine disorders, gastrointestinal disorders, infectious diseases, mental health, neurology oncology, etc.
  • Strong communication and interpersonal skills.
  • Bachelors/advanced degree or equivalent education/degree in life sciences/healthcare.
  • Experience from the pharmaceutical /CRO industry.
  • Ability to work independently and lead projects.
  • Strong analytical skills.
  • Commitment to highest quality outputs, including high attention to detail.
  • Ability to manage variable workload.

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Company/Employer
Parexel
Additional Info
Min. Experience
-
Job Location
Remote
Job Type
Full-time
Job Duration
Any
Language(s)
English
Est. Budget/Pay Rate
To be discussed
Est. hrs
-
Optimal Job Start
-
Applicant Countries
India,
Job Ref
J24B53FE41990