- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …of employee and/or contractor-based staff/analysts to support the overall delivery of a clinical trial diversity and patient access strategy. Qualifications: ... mechanisms at the study team and clinical trial site level to proactively monitor diversity ...experience required Experience Qualifications.7 or More Years 7 years clinical operations experience in trial diversity… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …meetings Serve on Clinical Trial Strategy Team in collaboration with Clinical Operations point, Clinical Director , and Field Medical Affairs point to ... for select clinical trials, in collaboration with Clinical Director and Clinical Operations...Medical Affairs team on relevant disease state topics and clinical trial data. Review and approve resources… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …internal and external partners, identify, qualify, manage, and maintain relations with clinical trial sites, including collaboration with PIs and patient ... advanced degree is preferred A minimum of 12 years' progressively responsible clinical trial experience within a pharmaceutical, biotechnology, CRO and/or… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …employer including veterans and people with disabilities. Summary The Associate Director , Clinical Data Standards, is responsible for the development, ... pipeline.Proactively identify Data Standards gaps and resolve issues related to clinical data standards development throughout the trial lifecycle.Standardize… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …investigators is expected. The CS Group Lead will also ensure the writing of high-quality clinical trial protocols, review of clinical data and Clinical ... Innovation 110 Years and Counting! Company is committed to diversity and inclusion. We are an equal opportunity employer...Clinical Science Asset Leaders (CSALs) at the Senior Director level for each respective program. This Clinical… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …medicinal product dossiers (IMPD), investigational new drug applications (IND), clinical trial applications (CTA), marketing authorization applications (MAA), ... clinical development and regulatory requirements of a clinical program. The Director will provide high...committed to creating an inclusive culture that celebrates the diversity of our employees, the patients we serve and… more
- Merck & Co. (North Wales, PA)
- …and retention efforts to achieve study milestonesUpon request from Global Clinical Trial Operations (GCTO),Recommends study sites and identifies potential ... to 50% travel required with some overnight.Role Summary The Regional Medical Scientific Director - GI Oncology is a credentialed (ie, PhD, PharmD, DNP, MD)… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …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 ... in the unique opportunity to bring highly innovative pharmaceutical products through clinical development to market. The candidate is a team player, detail oriented… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …degree preferred A minimum of ten (10) years of progressively responsible clinical trial experience within a pharmaceutical, biotechnology, or CRO required, ... About the Department The Clinical Development, Medical and Regulatory (CMR) department at...processes (ie automation, technology, process optimization). Relationships Reports to Director or above within CMR Training & Knowledge Management.… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …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 ... and other internal stakeholders Perform or supervise regulatory review of all clinical and nonclinical documents for submissions, eg, clinical protocols and… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …decisions (phase I trials) Provide safety input to Product Development Plan (PDP), Trial Outline, Protocol, Clinical Trial Report, Investigator's Brochure ... Relationships This position will report to Senior Global Safety Lead/ Director /Senior Director - Safety Surveillance, US East...Responsible for all areas related to patient safety in clinical trials Act as member of the trial… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …reports (CSR) Investigator brochures (IB) Informed consent and assent forms Lay summaries of clinical trial results Clinical evaluation plans (CEP) and ... program. Relationships The Senior Medical Writer reports to a Director of Medical Writing. The Senior Medical Writer is...to detail to ensure the accuracy and consistency of clinical trial documents A strong foundation in… more
- Novo Nordisk Inc. (New York, NY)
- About the Department The Clinical , Medical and Regulatory (CMR) department at Novo Nordisk is one of the most diverse and collaborative groups within the ... commensurate with eperience. The Position Builds relationships and demonstrates the clinical outcome and benefits of Novo Nordisk Inc., (NNI) products. Educates… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …is preferred A minimum of eight (8) years of progressively responsible clinical development/ trial experience within a pharmaceutical, biotechnology, or CRO ... About the Department The Clinical Development, Medical and Regulatory (CMR) department at...share resources across multiple groups. Relationships Reports to Associate Director or above within CMR Training & Knowledge Management.… more
- University of Maryland, Baltimore (Baltimore, MD)
- …(UM-IHC) is recruiting for a tenure-track physician-scientist with expertise in clinical trial design and execution to serve as Director of Clinical ... **Faculty* **Organization:** **School of Medicine - Centers/Programs/ORCs* **Title:** *Physician-Scientist, Director Of Clinical Trial Innovation… more
- Actalent (Boston, MA)
- Seeking a Senior Clinical Trial Manager to join a...CROs and vendors. This position will report to the Director of Clinical Operations. Must haves: + ... + Minimum of 5-8 years experience working in a Clinical Trial Manager capacity Responsibilities: + Serves...and Europe, Actalent serves many of the Fortune 500. Diversity , Equity & Inclusion At Actalent, diversity … more
- University of Utah (Salt Lake City, UT)
- …City, UT **Track** **New Position to Begin** As soon as possible **Details** ** CLINICAL TRIAL AND TRANSLATIONAL RESEARCH , BREAST MEDICAL ONCOLOGY** **Huntsman ... post-doctoral training; 2) Must have an established track record of clinical trial leadership/enrollment and scientific accomplishments with extramural industry… more
- University of Colorado (Aurora, CO)
- …to oversee planning, management, and execution of trial activities. At the Director level, this role will strategically lead clinical research operations for ... and manage long- and short-term strategic planning in direct support of ongoing clinical trial advancements and operations. + Manage strategic staffing for … more
- AbbVie (CA)
- …Development Plan and is responsible for: + Ensuring alignment between the IEST, and Clinical Trial Team(s) + Developing the proposed clinical milestones with ... Follow Allergan Aesthetics on LinkedIn. Job Description The Associate Director , Clinical Development will have global or...the project-related clinical development budget with the Clinical Trial Team and Project Manager +… more
- Boehringer Ingelheim (Ridgefield, CT)
- …clinical evidence team. The CDOL is accountable for maintaining standards across clinical trial documents and processes within an assigned indication or ... to avoid redundancies and improve efficiency. CDOL is responsible for collaborating with Clinical Trial Supply Unit in determining a comparator sourcing strategy… more
