Medical Writing/Research Analyst
Remote / Online - Candidates ideally in
505101, Kannur, Telangana, India
Listed on 2026-01-12
505101, Kannur, Telangana, India
Listing for:
DAVA Oncology
Remote/Work from Home
position Listed on 2026-01-12
Job specializations:
-
Research/Development
Research Scientist, Clinical Research, Research Analyst, Medical Science
Job Description & How to Apply Below
Location: Kannur
Work Hours:
U.S. time zones – requires evening/night shifts in India
DAVA Oncology is a fast-growing oncology-focused consulting company headquartered in Dallas, Texas. We are recruiting for a Medical Writer and Research Analyst to join our team remotely from India . This is a fully remote position , but working hours will be based on U.S. time zones , meaning evening and night shifts will be required.
Our team members have the opportunity to work in a variety of areas, including but not limited to: clinical trial research and communications, drug or trial publication research and review, and oncology conference meeting reviews. Candidates with previous experience in the oncology therapeutic area are highly desirable.
Responsibilities:
Conduct secondary research and acquire information from internet sources, compiling it into content.
Interpret, analyze, and compile proprietary data in a way that delivers a compelling scientific story.
Research, write, edit, and proof protocols, reports, and publications .
Maintain a strong scientific understanding of oncology (or the ability to quickly gain such understanding).
Prepare materials for major cancer conferences and internal oncology meetings .
Qualifications:
At least 1 year of experience in oncology-focused research or writing is preferred; publication planning experience is a plus.
Ph.D. in biology, biochemistry, organic chemistry, immunology, molecular biology, biotechnology, Pharm.
D. , or other related fields.
M.S. degree holders in the above fields with exceptional experience will also be considered.
Authorship in prestigious, peer-reviewed journals is highly preferred.
Experience in planning, writing, and reviewing study designs, protocols, data analysis, study reports, and regulatory documents is a plus.
Industry experience (pharmaceutical companies, CROs, etc.) is highly preferred.
Skills & Proficiencies:
Must be available to work during U.S. business hours (evening/night shifts in India).
Strong written and oral communication skills ; ability to explain technical concepts clearly.
Advanced knowledge of Microsoft Office Suite .
Ability to work independently and collaboratively on multiple projects with tight deadlines.
Highly motivated, organized, and detail-oriented self-starter.
Availability to work U.S. hours (evening/night shifts in India).
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