- Merck & Co. (North Wales, PA)
- …portfolio and compliance with public disclosure of clinical trials and their results. The Senior Informed Consent Medical Writer is responsible for ... internal policy, regulatory requirements, and health literacy principles.With minimal oversight, the Senior Informed Consent Medical Writer:Demonstrates… more
- Merck & Co. (North Wales, PA)
- …portfolio and compliance with public disclosure of clinical trials and their results. The Senior Informed Consent Medical Writer is responsible for ... policy, regulatory requirements, and health literacy principles.With oversight, the Informed Consent Medical Writer:Demonstrates growing independence… more
- Merck (North Wales, PA)
- …portfolio and compliance with public disclosure of clinical trials and their results. The Senior Informed Consent Medical Writer is responsible for ... regulatory requirements, and health literacy principles. **With minimal oversight, the Senior Informed Consent Medical Writer:** + Demonstrates… more
- Merck (North Wales, PA)
- …portfolio and compliance with public disclosure of clinical trials and their results. The Senior Informed Consent Medical Writer is responsible for ... regulatory requirements, and health literacy principles. With oversight, the Informed Consent Medical Writer: + Demonstrates growing independence managing… more
- University of Pennsylvania (Philadelphia, PA)
- …inpatient hospital setting; screen/enroll eligible subjects 5 days/week, in-person; obtain informed consent from study subjects or their proxies (in-person ... study enrollment packets. + Approach all eligible subjects every weekday and obtain informed consent . + Collection of multiple sets of human or environmental… more
- University of Pennsylvania (Philadelphia, PA)
- …support to Investigators and research staff in the development of research protocols, informed consent forms, case report forms, and other related study ... Pennsylvania. The Clinical Research Quality Specialist will work with senior team members to facilitate and conduct high quality...monitoring or auditing of studies + Development of protocols, consent forms, and case report forms + Coordination of… more
- Pfizer (Collegeville, PA)
- …other clinical and medical colleagues, with authoring protocols, study level informed consent documents, site training materials, and other clinical and ... disease area(s) of assignment. + Support other clinical and medical colleagues, clinical operations and other functional lines for...of the drug, keeping the clinical and safety colleagues informed of changes in the safety profile as they… more
- Pfizer (Collegeville, PA)
- …integrity and quality of the clinical trial(s). + Authors protocols, study level informed consent documents, and contributes to authoring of IBs, site training ... area(s) of assignment. + Partners with other clinical and medical colleagues, clinical operations and other functional lines for...of the drug, keeping the clinical and safety colleagues informed of changes in the safety profile as they… more
