- Eisai, Inc (San Francisco, CA)
- …confidence in discussing drug information/ disease state management. Prior experience in clinical research , drug development and/or clinical pharmacy ... MSL , 8+ years of overall experience in Oncology with relevant combination industry/ clinical / research / academia; at least 5 years as an MSL in Oncology… more
- Merck & Co. (Rahway, NJ)
- … to support decisions regarding safety and efficacy as well as new drug applications, clinical study reports, or publication;Participation in internal ... Clinical Research , Clinical Research Management, Clinical Studies , ...Clinical Studies , Clinical Testing, Clinical Trials, Data Analysis, Decision Making, Drug … more
- Merck & Co. (Rahway, NJ)
- …studies to support decisions regarding safety and efficacy as well as new drug applications, clinical study reports, or publication; andParticipation in ... post-licensure).The Senior Director will manage the entire cycle of clinical development, including study design, placement, monitoring,...Clinical Oncology, Clinical Research , Clinical Sciences, Clinical Studies , … more
- Merck & Co. (Boston, MA)
- … to support decisions regarding safety and efficacy as well as new drug applications, clinical study reports, or publicationParticipation in internal ... biomedical research experience in academiaDemonstrated success in overseeing clinical studies and protocolsDemonstrated record of scientific scholarship and… more
- Merck & Co. (Rahway, NJ)
- … to support decisions regarding safety and efficacy as well as new drug applications, clinical study reports, or publicationParticipating in internal ... the Senior Director will manage the entire cycle of clinical development, including study design, initiation, execution,... Clinical Research , Clinical Research Management, Clinical Studies , … more
- Merck & Co. (San Diego, CA)
- …(eg, study team, country teams, vendors, committees) in support of clinical study objectives.-Accountable for managing any study specific partners ... and key strategic engagements. This includes the ability to:Solid knowledge of clinical research regulatory requirements (eg, GCP and ICH)-Ability to manage… more
- Translational Research in Oncology (Los Angeles, CA)
- …updates and common site trends to Monitoring Resources and Project Management Departments Oversee study drug management at clinical study sites ... If you are an experienced Clinical Research Associate who is passionate...a timely manner to ensure clean data availability for studies analyses Input and maintain study information… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …to ensure the effective and efficient execution of operational aspects of clinical study planning, implementation, data delivery and reporting. Will represent ... relevant to the Clinical Operations function. Will ensure that global and local clinical studies are executed, in adherence to Good Clinical Practices… more
- Merck & Co. (Upper Gwynedd, PA)
- … studies to support decisions regarding safety and efficacy as well as new drug applications, clinical study reports, or publication; and participating in ... report to an Associate Vice President in the Oncology Clinical Research Group. Under the guidance of...of Clinical Scientists in the execution of clinical studies . --Work closely with a cross-functional… more
- Monster (Chattanooga, TN)
- …Strong attention to detail Strong leadership qualities Provide clinical oversite to study team Clinical research experience Ref: #568- Clinical ... Title: Clinical Research Physician / Principal Investigator...protocols according to FDA regulations and GCP guidelines Evaluate study volunteer's eligibility for clinical trials Perform… more
- Merck & Co. (Rahway, NJ)
- …in quality management or business management is preferred.Prerequisites:Minimum of 6 years in clinical research including at least 2 years with developing and ... 25%Flexible Work Arrangements:RemoteShift:1st - DayValid Driving License:NoHazardous Material(s):NoRequired Skills:Adaptability, Clinical Quality Management, Clinical Study … more
- Merck & Co. (Rahway, NJ)
- …and key strategic engagements. This includes the ability to:Solid knowledge of clinical research regulatory requirements (eg, GCP and ICH)Ability to manage ... writing, and presentation skillsEducation/ExperienceBachelor's Degree +5 years of pharmaceutical, clinical drug development, project management, and/or medical… more
- Merck & Co. (North Wales, PA)
- …and medical monitoring of clinical studies .Supervises development of clinical documents including protocols, clinical study reports and background ... Documentation, Clinical Investigations, Clinical Judgment, Clinical Reporting, Clinical Research , ... Research , Clinical Trial Documentation, Clinical Trial Planning, Consultative Approach, Cross-Cultural Awareness, Drug… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …focused on providing novel therapies in oncology, as well as other research areas centered around rare diseases and immune disorders. Summary: This position ... is responsible for enabling the on-time delivery of clinical supplies across the DSI portfolio. This role is...supporting CSO Project Management Leads by developing and updating Study Supply Plans, managing various work streams with key… more
- Eisai, Inc (Nutley, NJ)
- …external partnerships to equip and adapt the workforce to evolving technologies.Align clinical portfolio, business strategy, clinical studies , and related ... in neurology and oncology, with a strong emphasis on research and development. Our history includes the development of...your profile, we want to hear from you. The Clinical Quality Assurance Professional (QAP) position is responsible for… more
- Merck & Co. (Rahway, NJ)
- …or Manufacturing O rganizations . - Facilitate manufacturing, packaging , and release of clinical supplies for clinical studies , assist in scale up ... Job DescriptionOur company's Pharmaceutical Sciences and Clinical Supply organization translates molecules to medicines, working from the discovery interface through… more
- Merck & Co. (Rahway, NJ)
- …studies to support decisions regarding safety and efficacy as well as new drug applications, clinical study reports, or publication; andParticipating in ... The Senior Director will manage the entire cycle of clinical development, including: study design, placement, monitoring,...Research , Clinical Research Management, Clinical Risk Management, Clinical Studies ,… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …focused on providing novel therapies in oncology, as well as other research areas centered around rare diseases and immune disorders. Job Summary: Reporting ... direction for respective interventional/non-interventional programs such as post marketing studies or post approval commitments, medical access programs.Partner with… more
- Statistics & Data Corporation (SDC) (Waltham, MA)
- … reports, interpreting analysis results, writing statistical sections of clinical study reports, and participating in meetings with drug regulatory agencies ... develop the more junior biostatistics staff members. Serve as a lead statistician on clinical studies and provide senior level peer review of work being… more
- Merck & Co. (South San Francisco, CA)
- …of complex therapeutics. - Preferred: Knowledge in cardiometabolic and/or ophthalmology clinical drug development programs Expert skills in experimental design, ... Material(s):n/aRequired Skills: Clinical Development, Clinical Pharmacology, Clinical Trial Designs, Data Modeling, Data Visualization, Drug … more
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