Medical Writer (Contractor)
About The Position
The Medical Writer creates documents pertaining to both pre-marketing & post-marketing clinical trials, medical affairs, and safety data to support product development, license application, and post-marketing maintenance. These documents include, but are not limited to, aggregate reports (e.g., Development Safety Update Reports, Periodic Safety Update Reports, Period Benefit Risk Evaluation Reports, Addendum to Clinical Overviews, New Drug Application Periodic Adverse Drug Experience Reports, Safety Update Reports, Canadian Annual Reports, etc.), Risk Management Plans, Signalling, Labelling documents, Clinical Study Reports, and Protocols. The individual will be an integral part of a group of safety professionals within Sitero and will closely collaborate with safety teams in Contract Research Organizations (CROs) and partners. He/she will need to maintain medical knowledge as required by the role, strong and current knowledge of drug safety and pharmacovigilance regulations, pharmacovigilance practices, safety surveillance, and risk-management practices.
Requirements
- Minimum 2 years of experience in Medical Writing
- Degree in Life Science/Pharma or Equivalent
Nice To Haves
- 2-6 years of experience in Medical Writing
- Proficient computer knowledge and computer keyboarding skills.
- Proficient with Microsoft Office Suite (Outlook, Word, Excel).
- Strong verbal, written and interpersonal communication skills.
- Strong organization and prioritization skills; able to multitask.
- Flexibility to adapt and meet fluctuating business priorities.
- Able to occasionally work extended and/or flexible schedule to meet client requirements.
- Ability to build relationships, collaborate and influence across disciplines within Sitero and with outside stakeholders.
- Excellent verbal, written and presentation skills.
- Innovative, collaborative, initiative-taker.
Responsibilities
- Analyses, reviews, and interprets safety data, both non-clinical and clinical and any other relevant sources
- Authoring and review of Aggregate reports (PSURs/PBRERs, PADERs/Annual Reports/ ACO/ DSUR) for submission to local and other Health Authorities
- Authoring and review of Risk Management Plans as needed.
- Authoring and Review of Clinical Documents like Clinical Study Reports, Protocols
- Qualitative and Quantitative Signal Assessment
- Performing literature search and presentation of relevant articles for the aggregate reports.
- Management and reconciliation of relevant process trackers
- Subject matter expert (SME) along with training and mentoring of individuals.
- Generation of Periodic Safety Line Listings (PSLL) from safety database
- Exposure in handling regulatory agency/ Pharmacovigilance Risk Assessment Committee (PRAC) inquiries.
- Providing reliable support for high priority Ad-hoc activities
- Ensuring that deliverables to the clients comply with the relevant regulatory requirements and are sent to the client within agreed timelines
- Collaborates with Regulatory Affairs to ensure appropriate reporting of pharmacovigilance and drug safety information to regulatory agencies and prescriber community
- Training and mentoring of Pharmacovigilance associates
Benefits
- Hourly rate commensurate with Drug Safety medical writing experience level
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What This Job Offers
Career Level
Mid Level
