- Merck & Co. (Rahway, NJ)
- …the lead clinical scientist on the clinical trial team.Collaborates with the Medical Writer on clinical/ scientific and regulatory documents. Partners with ... Job DescriptionThis position drives scientific planning, strategy and execution of Phase 1-4...includes the ability to:Apply strong knowledge of clinical research regulatory requirements (eg, GCP and ICH)Manage multiple competing priorities… more
- Merck & Co. (Rahway, NJ)
- …lead clinical scientist on the clinical trial team.Collaborates with the Medical Writer on clinical/ scientific and regulatory documents.Partners with Study ... DescriptionPosition Description: Associate Director, Clinical Scientist This position drives scientific planning, strategy and execution of Phase 1-4 clinical… more
- Hologic (San Diego, CA)
- Regulatory Scientific Writer San Diego, CA, United States Discover a career with real meaning. One that offers the opportunity to showcase your talents, ... lives everywhere, every day. Our Regulatory Affairs department is looking for a Regulatory Scientific Writer here in San Diego! In this role, you will be… more
- University of Miami (Miami, FL)
- …SCCC - Protocol Development Office (PDO) has an exciting opportunity for a Full Time Scientific Writer (Medical Writer ) to work Remotely. CORE JOB SUMMARY ... The Scientific Writer analyzes scientific ...of clinical trials including protocol and ICF development, institutional regulatory submissions (Protocol Review and Monitoring Committee [PRMC] and… more
- Houston Methodist (Houston, TX)
- At Houston Methodist, the Scientific Writer position is responsible for performing a variety of tasks including preparing laboratory and clinical studies and ... agency requirements. + Prepares moderately complex documents and sections of regulatory submissions and contributes scientific knowledge and analytical skills… more
- University of Miami (Miami, FL)
- …of Miami/UHealth Department of SCCC has an exciting opportunity for a Full Time Scientific Writer to work at the UHealth Medical Campus. The Scientific ... audiences. The role requires a strong background in grant writing and scientific manuscript development. Please submit a cover letter with your online application.… more
- MD Anderson Cancer Center (Houston, TX)
- …patient education/materials, IRB forms. Works collaboratively with research nurse manager and regulatory staff to develop or coordinate the development of the study ... patient education/materials, IRB forms. Works collaboratively with research nurse manager and regulatory staff to develop or coordinate the development of the study… more
- ThermoFisher Scientific (Mount Prospect, IL)
- …on both the patient and the product is assessed against applicable regulatory guidelines. + Identify and address activities and barriers associated with ... industry. + Minimum of 3 years of experience in technical or scientific writing principles. + Demonstrable knowledge of cGMP principles pertaining to investigations… more
- Abbott (Santa Clara, CA)
- …and interact with regulatory agencies' representatives as needed. The role of Scientific CER Writer /PM plays a significant part in new product development, ... fingersticks. **The Opportunity** The function of a **Senior Medical Writer /Project Manager** supporting our Vascular Clinical Evaluation Products combines… more
- J&J Family of Companies (Spring House, PA)
- …their potential. At Johnson & Johnson, we all belong. The Nonclinical Submissions Writer will prepare and review regulatory submission documents that summarize ... Nonclinical Submissions Writer , Preclinical Sciences and Translational Safety + Job titleNonclinical Submissions Writer , Preclinical Sciences and Translational… more
