- Acadia Pharmaceuticals Inc. (Princeton, NJ)
- …to work in our office three days per week on average. Position Summary: The Associate Director (AD), Clinical Trial Materials (CTM) plays a pivotal role in ... programs across Phase I-IV and investigator-initiated studies (IIS). Reporting to the Sr. Director of Clinical Trial Materials, this strategic and hands-on… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …submission documents under guidance of higher level. Reviews and oversee completion of clinical trial protocols. Provides medical and/or scientific direction ... to improve standards of care and address diversified, unmet medical needs of people globally by leveraging our world-class...Planning and Execution: Provides input on major milestones of trial , clinical trial plan and… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …(SP&L) function with assigned tasks related to steady supply of Clinical Trial Materials (CTM).ResponsibilitiesLead the authoring, revising, and managing ... pharmaceutical therapies to improve standards of care and address diversified, unmet medical needs of people globally by leveraging our world-class science and… more
- Merck & Co. (Chicago, IL)
- …and retention efforts to achieve study milestones.Upon Request from Global Clinical Trial Operations (GCTO)Recommends study sites and identifies potential ... Job DescriptionWe are seeking a Growth and Improvement minded Regional Medical Scientific Director ( Medical Science Liaison / MSL) - in Inflammatory Bowel… more
- Merck & Co. (OK)
- …and retention efforts to achieve study milestonesUpon request from Global Clinical Trial OperationsRecommends study sites and identifies potential investigators ... achieve study milestones.Protocol lead responsibilities in collaboration with Global Clinical Trial OperationsAddresses questions from investigators and provides… more
- Genmab (NJ)
- …synopsis, protocols, statistical analysis plans, results meetings presentations and clinical trial reportsCoordinate data transfers from/to business partners ... RoleThe Associate Director acts as a statistical expert supporting the clinical development of compounds as compound and/or indication lead for both early and… more
- Fred Hutchinson Cancer Center (Seattle, WA)
- …who are focused on mission-critical clinical trial programs. The Clinical Research IIT Program Director (Investigator-Initiated Trial ) is primarily ... three years of staff management experience and five years of experience in clinical trial /protocol management. Demonstrated knowledge of clinical research… more
- Ascendis Pharma (Palo Alto, CA)
- …of the Company's late-phase clinical trials in endocrinology. As such, the Medical Director is an important and visible member of the clinical ... for employees to grow and develop their skills. The Medical Director is involved in the design,...Ensure successful completion of trial -related documents (including clinical trial protocols, investigator brochures, medical… more
- Merck & Co. (South San Francisco, CA)
- …Develop model-based strategies ( translational PK/PD strategies, mechanistic model, POPPK/PD, clinical trial simulations, etc) for quantitative analyses, within ... all phases of drug development including, but not limited to dose selection, clinical trial design, and go/no-go decisions. Represent QP2 on cardiometabolic and… more
- Merck & Co. (South San Francisco, CA)
- …exposure-response models, quantitative system pharmacology (QSP) and disease progression models, clinical trial simulations, comparator modeling) that seek to ... Requirements: 25%Flexible Work Arrangements:Not ApplicableShift:Not IndicatedValid Driving License:NoHazardous Material(s):n/aRequired Skills: Clinical Trial Designs, Clinical … more
- Insmed Incorporated (Los Angeles, CA)
- …and development programs as requested by R&D, Clinical Operations, and Medical Affairs Departments. This may include trial site identification, ongoing ... has strong related experience.Other Pharmaceutical experience - Medical Information, Medical Strategy, Clinical management/ trial experience and 2 years… more
- BioSpace (Washington, DC)
- …Amgen team. Join us and transform the lives of patients while transforming your career. Clinical Research Medical Director , Uplizna What you will do Lets do ... input into safety and regulatory interactions. Interpret and communicate clinical trial data. Author/review CSRs, publications, and...Basic Qualifications: MD or DO degree from an accredited medical school AND 2 years of clinical … more
- Merck & Co. (Boston, MA)
- …pharmacokinetics (PK) and pharmacodynamics (PD) analysis, model-based meta-analysis (MBMA), clinical trial simulations (CTS), pediatrics modeling and disease ... our company, this position offers an opportunity for the Director to drive pipeline impact and mentor/coach a talented...seek to improve cycle time, cost/size, number of trials, clinical trial design and Go/No Go decisions… more
- Eisai, Inc (Nutley, NJ)
- …plan. Provide strategic development, planning, implementation and oversight of Phase IV clinical trial programs within the Medical Affairs department ... your profile, we want to hear from you. The Medical Director will provide medical ...in relevant therapeutic area. Substantial experience across areas of Medical Affairs' functions or phase II/III/IV clinical … more
- Eisai, Inc (Nutley, NJ)
- …training (eg medical insights workshops, presentation skills, understanding clinical trial design, statistics, etc.) to supplement MSL ... profile, we want to hear from you. The Associate Director (AD), Global Medical Affairs Training and...regional medical directors and MSL leadership, Publications, Medical Communications, Clinical Development, Biostatistics, Field HEOR,… more
- Merck & Co. (San Francisco, CA)
- …(popPK), PK/PD models, exposure response (ER) models, model-based meta-analysis (MBMA), clinical trial simulations (CTS) and disease progression modeling into ... Company, this position offers an opportunity for the Associate Director to drive pipeline impact across therapy areas. -...seek to improve cycle time, cost/size, number of trials, clinical trial design and Go/No Go decisions… more
- Johnson and Johnson (Irvine, CA)
- … device industry, and is familiar with pertinent regulations and guidelines governing clinical trial execution and clinical data publication. You will ... are currently seeking the best talent for an Associate Director , Clinical Science & External Research (CSER)...required ; PhD/MD/ PharmD strongly preferred. 10-12 years of clinical , medical affairs or related technical experience… more
- Eikon Therapeutics (Millbrae, CA)
- … operations and FSP study management teams. You possess a deep understanding of clinical trial regulations, guidelines, and the principles of Good Clinical ... intractable classes of proteins as drug targets. Position The Director of Clinical Operations Study Management will...(GCP), ensuring strict compliance throughout the clinical trial process. What You'll Do In collaboration with senior… more
- Merck & Co. (San Francisco, CA)
- …Arrangements:HybridShift:Valid Driving License:Hazardous Material(s):Required Skills:Budget Development, Business, Clinical Supply Chain Management, Clinical ... Job Description Position Description: Associate Director , DSCS Digital Implementation Project ManagerWithin the Development Sciences and Clinical Supply (DSCS)… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- … and screen failures. Clinical trial protocol development and reviews ( clinical trial protocols and medical device protocols)ICF reviews to ensure ... pharmaceutical therapies to improve standards of care and address diversified, unmet medical needs of people globally by leveraging our world-class science and… more
Related Job Searches:
Clinical,
Clinical Director,
Clinical Trial,
Director,
Medical,
Medical Director,
Medical Director Clinical,
Trial