Instagram
youtube
Facebook

Medical Writer

1-6 years
Not Disclosed
15 June 13, 2024
Job Description
Job Type: Full Time Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Are you seeking a purposeful and rewarding Medical Writing career opportunity?

 

Our Cardiac Safety, Respiratory & Precision Motion teams are growing in India, and with big ambitions and a clear vision for the future, now is the time to join Clario as a Medical Writer.

 

These positions are subject to Indian, European and US working hour shift patterns, and are considered hybrid working roles from our offices in VG Heritage, 18/2, 18/3, Vani Vilas Road, Basavanagudi, Bangalore 560004.

 

What we offer:

  • Competitive compensation + shift allowances

  • Attractive benefits (security, flexibility, support and well-being)

  • Engaging employee programs

  • Technology for hybrid working and great onsite facilities

 

What you'll be doing:

 

The Medical Writer is responsible for working with the Statistical and Scientific teams to create Expert Reports and Statistical Analysis Plans as well as assist with synopsis and protocol development.

  • Create, edit/proofread, and finalize Expert Reports based on the output of the statistical analysis (Tables, Listings, and Figures) and the final conclusions of the Scientific team.

  • Work with the Statistical team to create, edit/proofread, and finalize the Statistical Analysis Plan(s).

  • Work with the Statistical and Scientific teams to help sponsors with the development of synopsis and protocols for the cardiac safety component

  • Overall management of timelines of all deliverables in terms of Expert Reports, Statistical Analysis Plans, and other outputs as needed

  • Understand FDA/EMA regulations in regards to clinical trial reporting

 

What we look for:

  • Bachelor’s Degree in Science or Healthcare related field

  • At least five years of previous experience in medical or scientific writing for publications, reports, or grant submissions

  • Excellent English language skills (writing, reading, verbal)

  • Knowledge of clinical trials environment and regulations

 

At Clario, we put people first, always. We are united and driven by patients, committed to making a difference, and we are always looking for the best talent to help us transform lives. We value the contribution each of our people brings. It’s only through our people that we can continue to innovate technology that will shape the future of clinical trials.