bioclinica
Associate Medical Writer
Princeton, NJ, United States · Staff+
Sponsorship not specifiedDetected 2356 days ago
Project ManagementExcelResearchCommunicationTime ManagementPublic SpeakingOrganizational SkillsMicrosoft Office
About the role
- Company Description Bioclinica is one of the leading global CRO company which focuses on bringing efficiency to the clinical trials.
- We have a premier global research network-and the only one with investigator sites in the U.S., Europe, Latin America, and Asia.
- Bioclinica offers a network of research sites, patient recruitment-retention services, and a post-approval research division.
Responsibilities
- Creating, modifying, and finalizing Key Points Documents (KPDs) from CRs
- Creating, modifying and finalizing paper Source Documents based on ToOs
- Attending internal and external meetings relating to the Site Manuals, IQA/PQA/QC Summaries, CRs/KPDs, Source Documents and any other MedComm-related study start-up documents
- Maintaining MedComm document webpages
Requirements
- Providing language updates, as required, for all MedComm document templates as needed
- Ability to work in a group setting and independently
- ability to adjust to changing priorities
- Documenting study-specific Protocol Training (Kick-off Meeting Slides, Protocol Overview Presentations, etc.) by filling out and collecting signatures on group training forms as required
Nice to have
- Bachelor's Degree in either the Life or Physical Sciences (e.g., Biology, Chemistry, Physics, Pharmaceutics, etc.) preferred
- 2+ years of experience in pharmaceutical/clinical/imaging research preferred
- Proficiency in MS Office Suite (Word, Excel, Outlook, PowerPoint, Access)
Company info
- Company Description
- Bioclinica is one of the leading global CRO company which focuses on bringing efficiency to the clinical trials.
- We are headquartered in Doylestown, PA.
- We serve more than 400 pharmaceutical, biotechnology, and device organizations
- Staying up-to-date on response criteria publications posted by Medical Communications
- Participating in Medical Writing Training activities, including creating/reviewing training modules
- Participating in Clinical Project Management Training activities, including creating/reviewing training modules
- Attending and participating in applicable company-sponsored training
Equal opportunity
- Bioclinica is an equal opportunity employer.
- EEO Statement
- equal opportunity employer.
Visa & Work Authorization
- ical Project Management Team, including the review of Project-Specific Work Instructions and attending document-related Sponsor calls
Apply directly at bioclinica →Create a free account for alerts like thisView bioclinica immigration profile
This listing is sourced directly from bioclinica's careers page and normalized into a canonical job model.