PSG Global Solutions Careers
Medical Writing Manager
PSG Global Solutions Careers, South San Francisco, California, us, 94083
Apply now and our proprietary system will quickly have you in front of a live recruiter.The OpportunityDescriptionWe're looking for a
Medical Writing Manager , working in
Pharmaceuticals and Medical Products
industry in
455 Mission Bay Boulevard, South San Francisco, California, 94158, United States .
Job description:Writes and edits clinical reports, summarize data from clinical studies for submissions to the FDA and for publication and/or presentation.Contributes to the development of formats medical writing infrastructure.Remains informed of the latest professional, technological, and regulatory developments in medical writing, as well as therapeutic areas.Supports all clinical writing activities outlined in the Project Clinical Development Plans (CDPs).
Our Client
Our client is an award-winning clinical development company. Improving lives globally with 20+ years experience in clinical research and strategic resourcing. Elevating results with proven strategies, comprehensive solutions, and customized delivery models.
Serving pharmaceutical, biopharmaceutical, biotechnology, and medical device organizations.
Strong relationships provide you connections and access to great opportunities. Industry expertise sets you up for success with helpful insights, career coaching, and professional training. Grow and learn while you put your skills to work.
Experience Required for Your Success
Bachelors/Masters degree in a scientific discipline with a strong journalism background is required (Equivalent experience may be accepted)8 years in a pharmaceutical, biotech, or CRO medical writing position is required6 years writing management experience is also requiredAbility to create effective presentations from raw data is essentialAbility to interpret statistical and clinical data is a plusAbility to work well with others in high-pressure situationsMust have demonstrated problem solving abilitiesStrong organizational skills are requiredStrong written and verbal communication skills are requiredUnderstanding of clinical research, biostatistics, and regulatory affairs is requiredExperience writing clinical protocols, clinical study reports, and IND sectionsGood computer skills are requiredWorking knowledge of MS word, Excel, Power point, Project, and Outlook is a plus
What Do You Think?Does your experience reflect what it takes to be successful in this role? Do the work and challenges get you excited about what's possible?
Medical Writing Manager , working in
Pharmaceuticals and Medical Products
industry in
455 Mission Bay Boulevard, South San Francisco, California, 94158, United States .
Job description:Writes and edits clinical reports, summarize data from clinical studies for submissions to the FDA and for publication and/or presentation.Contributes to the development of formats medical writing infrastructure.Remains informed of the latest professional, technological, and regulatory developments in medical writing, as well as therapeutic areas.Supports all clinical writing activities outlined in the Project Clinical Development Plans (CDPs).
Our Client
Our client is an award-winning clinical development company. Improving lives globally with 20+ years experience in clinical research and strategic resourcing. Elevating results with proven strategies, comprehensive solutions, and customized delivery models.
Serving pharmaceutical, biopharmaceutical, biotechnology, and medical device organizations.
Strong relationships provide you connections and access to great opportunities. Industry expertise sets you up for success with helpful insights, career coaching, and professional training. Grow and learn while you put your skills to work.
Experience Required for Your Success
Bachelors/Masters degree in a scientific discipline with a strong journalism background is required (Equivalent experience may be accepted)8 years in a pharmaceutical, biotech, or CRO medical writing position is required6 years writing management experience is also requiredAbility to create effective presentations from raw data is essentialAbility to interpret statistical and clinical data is a plusAbility to work well with others in high-pressure situationsMust have demonstrated problem solving abilitiesStrong organizational skills are requiredStrong written and verbal communication skills are requiredUnderstanding of clinical research, biostatistics, and regulatory affairs is requiredExperience writing clinical protocols, clinical study reports, and IND sectionsGood computer skills are requiredWorking knowledge of MS word, Excel, Power point, Project, and Outlook is a plus
What Do You Think?Does your experience reflect what it takes to be successful in this role? Do the work and challenges get you excited about what's possible?