- Merck & Co. (North Wales, PA)
- …decisions regarding safety and efficacy as well as new drug applications, clinical study reports, or publicationParticipation in internal and joint ... Vice President will manage and oversee the entire cycle of clinical development, including study design, initiation, execution, monitoring, analysis, regulatory… more
- Merck & Co. (North Wales, PA)
- …clinical documents including development plans, protocols, trial related documents, clinical study reports and background documents.Interfaces with functional ... Job DescriptionThe Associate Vice President (AVP)/Section Head, Global Clinical...into research and business development priorities and prioritization of clinical assets.-May serve as the senior liaison… more
- Merck & Co. (North Wales, PA)
- Job DescriptionReports to the Director/ Senior Director in the Office of Promotion and Advertising Review (OPAR)The Associate Director is responsible for the ... promotional messages and claims (aligned with marketing strategy) in clinical trial design and product labeling as it relates...product labeling as it relates to the use of study results in US promotion.Maintain current awareness of evolving… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …of all clinical and nonclinical documents for submissions, eg, clinical protocols and study reports, preclinical reports, investigator brochures, application ... MA and Plainsboro, NJ. We support programs from early research through late-stage clinical development. We are building for the future, creating a distinct R&D… more
- WuXi AppTec (Philadelphia, PA)
- **Overview** The Clinical Research Associate III Senior Oncology performs and coordinates aspects of field-based and office-based monitoring and data quality ... **Essential Job Functions:** + Responsible for all aspects of clinical monitoring and required reporting, including pre- study ...or supervisor, including but not limited to mentoring of Clinical Research Associate (CRA) I and II… more
- Abbott (Philadelphia, PA)
- … clinical sites and other Abbott clinical staff (eg, operations management, study team, Site Contracts Associate ), as needed. **Manage all aspects of ... working mothers, female executives, and scientists. **The Opportunity** The ** Associate Clinical Site Lead** for the Philadelphia,...needed, provide clinical and technical expertise for clinical trial procedure support + Attend study … more
- Bristol Myers Squibb (Princeton, NJ)
- …at work and in their personal lives. Read more: careers.bms.com/working-with-us . The Associate Director, Clinical Data Standards is a leadership role with ... Director or Executive Director, Head Standards Management & Steward within Clinical & Safety Data Insights and Analytics. **Position Responsibilities** + Providing… more
- Bristol Myers Squibb (Princeton, NJ)
- …and at governance meetings based on proficiency + **Provide input** to Phase 2/3 clinical study design and registrational strategy + **Accountable for the** ... Clinical Pharmacology Plan + **Lead** design of clinical pharmacology studies and manages data analysis, interpretation, and reporting + **High proficiency**… more
- Penn Medicine (Philadelphia, PA)
- …work? ** Senior Imaging Informatics Support Analyst-** Job Summary: + The Senior Imaging Informatics Analyst on the Clinical Imaging Team is responsible ... Monitoring and Patient Information Management: + 1. Correct studies , when images are in the wrong study...hospital's Radiology, Cardiology or IT department or relevant Radiology Clinical Experience. + Bachelor's or Associate 's degree… more
- Bristol Myers Squibb (Princeton, NJ)
- …we pioneer. Join us and make a difference. **Summary/Scope** Reporting to Senior Scientific Director Translational Medicine, the TM Sr . Principal Scientist ... late stage TM group. The individual will be responsible for TM and clinical biomarker activities to support drug development programs in multiple diseases in… more
- University of Pennsylvania (Philadelphia, PA)
- …responsibilities may include scientific leadership of managing and integrating data for clinical trials and observational studies ; assist with grant writing; ... at the University of Pennsylvania seeks candidates for an Associate or Full Professor position in either the non-tenure...services to facilitate the collection, storage, and management of clinical research data for any size research study… more
- University of Pennsylvania (Philadelphia, PA)
- …that fall within the scope of currently funded grants. Working alongside the Associate Director of Immunology, the Senior Research Investigator will design, plan ... bench. Working in partnership with the Principal Investigator and Associate Director of Immunology, the Senior Research...work with other members of the lab, including the Associate Director(s) of Clinical Research and Translational… more
- Bristol Myers Squibb (Princeton, NJ)
- …our new drugs in patients. We are seeking a talented and highly motivated Senior Associate Scientist interested in a fast-paced scientific environment and with a ... a large cross-functional team. **Position Responsibilities** In the role as a Sr . Associate Scientist within Translational Early Development Genomics team, the… more
- Bristol Myers Squibb (Princeton, NJ)
- …Reporting to Senior Scientific Director Translational Medicine (TM), the TM Associate Director will be part of the late stage TM group. The individual ... will be responsible for TM and clinical biomarker activities to support drug development programs in...lead responsibilities such as serving as biomarker representative on study teams, setting up biomarker plans for individual trials… more
- Penn Medicine (Radnor, PA)
- …Working for this leading academic medical center means collaboration with top clinical , technical and business professionals across all disciplines. Today at Penn ... each day. Are you living your life's work? Entity: Clinical Practices of the University of Pennsylvania (CPUP) Department:...well as supply information to patients enrolled in these studies . + Schedule follow up studies as… more
- Intra-Cellular Therapies, Inc (Bedminster, NJ)
- …data to provide statistical interpretation for clinical reports and contribute to clinical study designs. + Over time, with mentorship, provide support to ... of approved and investigational compounds across different stages of clinical development. Our lead candidate, lumateperone (CAPLYTA(R)), is FDA-approved for… more
- Merck (North Wales, PA)
- …to support decisions regarding safety and efficacy as well as new drug applications, clinical study reports, or publication + Participation in internal and joint ... **Job Description** The Associate Vice President (AVP) has primary responsibility for...President will manage and oversee the entire cycle of clinical development, including study design, initiation, execution,… more
- Merck (Upper Gwynedd, PA)
- **Job Description** The ** Senior Clinical Director ( Sr . Principal Scientist)** has primary responsibility for the strategic planning and directing ... in Immunology. With a focus on late-stage development, the Senior Clinical Director will manage the entire...safety and efficacy as well as new drug applications, clinical study reports, or publication; and +… more
- Merck (Upper Gwynedd, PA)
- …projects, including pipeline candidates and licensed products + Supervises development of clinical documents including protocols, clinical study reports and ... **Job Description** The Associate Vice President (AVP)/Section Head, Global Clinical...development of assets within the Respiratory Section of Global Clinical Development + May serve as a senior… more
- ICON Clinical Research (Blue Bell, PA)
- …highly qualified CRAs to identify, select, initiate and close-out investigational sites for clinical studies in phases II - IV, ensuring adherence to applicable ... clinical development. We are currently seeking a Clinical Research Associate II to join our...submissions as requested + Participate in preparing and reviewing study documentation and feasibility studies for new… more
