Medical Writer Jobs in New Jersey
A Medical Writer in the biotechnology industry plays a vital role by creating clear and comprehensive documentation that communicates complex scientific information effectively. They develop a range of documents, including research reports, clinical study protocols, regulatory submissions, and educational materials. Accuracy, clarity, and consistency are paramount in their writing, which requires a deep understanding of scientific methodologies and terminologies. They also need to be updated with current regulatory guidelines and ethical considerations.
Essential skills for a Medical Writer include excellent written and verbal communication, a keen attention to detail, and the ability to present complex data in an understandable manner. They should possess a strong background in life sciences, and often, a Bachelor's or Master's degree in a scientific or medical field is required. Certification from organizations like the American Medical Writers Association (AMWA) or the European Medical Writers Association (EMWA) can further enhance their credibility. Preceding job roles that could lead to a career as a Medical Writer may include Clinical Research Associate, Regulatory Affairs Specialist, or Scientific Editor.
Principal Medical Writer II Job Description The Associate Director, Principal Medical Writer II is responsible for developing clinical documents for submissions to regulatory authorities globally....
Remote WorkProvide training and mentorship to junior Medical Writers and Editors, offering guidance on best practices in medical writing and editing....
We have a robust pipeline of ADCS in clinical trials for both hematologic and solid tumor cancers....
Job Title: Principal Medical Writer II Job Description The Associate Director, Principal Medical Writer II is responsible for developing clinical documents for submissions to regulatory authorities...
Remote WorkMSD Specialist Disclosure Medical Writer New Pay $85600.00 - $134800.00 / year Location Rahway/New Jersey Employment type Full-Time Job Description Req#: R347569 Employer Industry: Pharmaceutical Research...
of clinical trials and their results, document disclosure, and data sharing with external researchers....
The Specialist (Disclosure Medical Writer) will be primarily responsible for preparing clinical study registration and results disclosure postings in compliance with company policy and country laws...
As a Senior Medical Writer, you will provide technical consultation and advice on strategy, regulations and industry best practices....
Minimum of 3 years of experience in medical editing or medical writing, preferably within a pharmaceutical advertising or experiential agency setting....
with NDAs and other regulatory submissions Knowledge of regulatory requirements and guidelines for clinical trials Proficiency in medical writing software and templates (i.e., EndNote, Starting Point...
Help to iteratively improve medical writing processes as appropriate....
EPM is partnered with an innovative global biopharmaceutical company that is looking for a Senior Medical Writer to join their US team in the NJ/NY area....
The Senior Medical Writer will have oversight of internal and external medical writing activities, create processes for the department, author key documents, and ensure timelines of critical deliverables...
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Medical Writer Online Courses and Training Opportunities
Salary for Medical Writer Jobs in New Jersey
Required or preferred licenses and certifications for Medical Writer positions.
Highest Education Level
Medical Writers in New Jersey offer the following education backgroundQualifications / Skill Sets
The following top skills are often required or desired to land a Medical Writer position
- English
- Adobe Acrobat
- Content Writing
- Publishing
- Grammar
- Writing Skills
- AMA Manual of Style
- Style Guides
- ICH GCP
- ICH Guidelines
- Medical Affairs
- Biostatistics
- Drug Discovery
- Drug Development
- Medical Writing
- Pharmacovigilance
- Immunology
- Scientific Writing
- Toxicology
- Clinical Trials
- Biotechnology
- Neuroscience
- Clinical Operations
- Clinical Research
- Oncology
- Medical Device Sales
- FDA Regulations
- Research and Development
- Standard Operating Procedures
- Technical Writing
- Medical Terminology
- Statistics
- Health Care
- Strategy Development
- Quality Control
- Investigation
- Auditing
- Microsoft Outlook
- Presentation
- Documentation
- Collaboration
- Interpersonal Skills
- Microsoft PowerPoint
- Regulations
- Project Management
- Problem Solving
- Teamwork
- Research Skills
- Microsoft Office
- Microsoft Excel
- Microsoft Word
- Time Management
- Staff Supervision
- Organization
- Scheduling
- Computer Skills
- Leadership
- Communication Skills
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