- Provide support in the development and execution of clinical tactics of Medical Affairs and Clinical affairs concerning any related clinical publication coming from IITs, Sponsored Trials, Clinical White Paper, Advisory Board Consensus and Resolutions, and Advisory Board Experts' Recommendations.
- Manage the overall development and approval process for assigned documents within timelines, including documentation generation, initiation of review process, discussions on proposed revisions, and document completion in collaboration with other team members
- This includes, but is not limited to: directing, authoring, editing, and providing input to scientific abstracts and manuscripts, presentations, posters, and publications
- Critically analyze complex information and collaborate with clinical and statistical teams on data description, presentation, and analysis
- This includes, but is not limited to: directing, authoring, editing, and providing input to scientific abstracts and manuscripts, presentations, posters, and publications.
- Critically analyze complex information and collaborate with clinical and statistical teams on data description, presentation, and analysis
- Work together with the Medical Experts in reinforcing clinical messages supporting the use of the Company Portfolio
- The candidate must have the ability to collaborate with diverse internal teams to map a product's needs for KOL engagement and to execute new business processes that impact internal strategy and external facing activities
- Bachelor's degree in Life Sciences required, and advanced degree preferred
- Minimum 3-5 years experience in similar Medical Affairs roles/ positions primarily regional roles in Publications, Medical Writing, and Clinical Trial Execution
- Experience in Pharmaceuticals, Life Science & Medical Devices industry is preferred
- Demonstrated ability to produce clear, concise, and effective written and verbal communications describing scientific and clinical data in English
- Understanding of clinical trial design and execution, statistical methods, and clinical trial data reporting requirements
- Ability to work collaboratively and coordinate the efforts of team members to resolve comments, and produce a final high-quality document
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Medical Writer - Singapore - PEOPLESEARCH PTE. LTD.
Description
Roles & ResponsibilitiesMedical Writer
Our client is one of the most diverse Pharmaceutical MNCs in the world. Rapidly expanding its operations in the Asia Pacific Region.
Roles & Responsibilities
Requirements
Location : West, Singapore
Kindly indicate your current/last salary details and your notice period
If the above speaks to you, we'd love to hear from you. Please send in your updated CV to (Gerard James Rozario, Reg No: R if you feel there is a fit with your experience and interest. You may forward this great opportunity to someone who would be a great fit for this role.
All information will be kept strictly confidential. We regret to inform that only successful applicants will be contacted.
PeopleSearch Pte Ltd
EA License No: 16S8057
Tell employers what skills you haveTactics
FDA
Clinical Research
CRO
Medical Writing
Approval Process
Clinical Development
Clinical Operations
Clinical Trials
Medical Affairs
Trials
Medical Devices
Publications
Life Sciences
Directing
