Job Description

• Katalyst Healthcares & Life Sciences is hiring entry level candidates for several positions for contract research in Clinical trials of drugs, biologics and medical devices.
• We have a few immediate job opportunities available in Drug Safety and Pharmacovigilance and Clinical Research field. We work with University hospitals, pharmaceutical companies and recruiting partners.

Job Description

Responsibilities:

• Prepare technical documents to support both domestic and international regulatory submissions.
• Incorporates text, graphs, charts, tables and statistical analysis. Proofreads, circulates, edits, assembles, inspects and duplicates product submissions. 5+ years exp.
• Innovative writing with extensive knowledge and understanding of clinical research.
• Able to succinctly summarize complex scientific publications and translate science to a lay audience.
• Excellent verbal and written communication skills in addition to good interpersonal skills (i.e., build relationships with cross-functional colleagues.
• Proficient in the use of Office 365 software such as PPT, Word, Excel, etc.
• Proficient in the use of graphics software, including Adobe Illustrator for Medical Writer II.
• Preferred for Medical Writer III but not required.
• Accurate in work, efficient, and contributes to process improvement.

Requirements:

• PhD in Sciences or Technology, PharmD, or MD for Medical Writer III with 5+ years of experience in medical or scientific writing.
• Have evidence of publications in peer-reviewed journals as first author and/or has written AMCP dossiers.
• Writers with prior experience in AMCP Format and AMCP Dossiers. Certification in oncology.
• Individual contributor with cross functional collaboration.

Additional Information

All your information will be kept confidential according to EEO guidelines.

Job Tags

Similar Jobs