- Russell Tobin & Associates (San Diego, CA)
- …years expeirence in medical device, pharma, IVD and/or CRO 5-8 years experience leading clinical study preparation and monitoring and leading study team ... What are we looking for in our Sr. Clinical Research Associate ? The Scientific Team...Proven track record in clinical study completion with adherence to timelines, budget, and milestones… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …rare diseases and immune disorders.Summary Assist in planning and execution of clinical studies , under the supervision of the Study Manager role the Study ... goals and milestones to monitor and ensure compliance with Daiichi Sankyo Clinical Study Oversight Plan (CSOP).Responsibilities- Reconcile the TMF document… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …equal opportunity employer including veterans and people with disabilities. Summary The Associate Director, Clinical Data Standards, is responsible for the ... improvement opportunities.Communicate and reinforce content and interpretation of Daiichi Sankyo's Clinical Data Standards to DS Project and Study teams,… more
- Sun Pharma (Taro Pharma) (Princeton, NJ)
- …CROs (eg Site identification, Feasibility, Site selection, Contract negotiation and Clinical Study Agreement finalization, Translations, EC and Regulatory ... Associate Director, Clinical Operations Sun Pharma...predefined timelines.Prepare and implement Quality control plan in assigned studies and ensure that clinical studies… more
- Novo Nordisk Inc. (WA)
- …North America Clinical Development (NACD) goals, including successful delivery of studies within the clinical trial portfolio. Contributes to local or ... About the Department The Clinical , Medical and Regulatory (CMR) department at Novo...The Position Drives the understanding and delivery of quality clinical research (patient safety, rights and wellbeing; data reliability;… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …and Modeling and Simulation plans, design and lead study teams to execute Clinical Pharmacology studies , conduct hands on population PK and PKPD analyses and ... documentsServes as a specialist in PK-PD and Pop PK-PD concepts, phase 1-4 clinical studies , literature, and regulatory guidelines and can conduct/develop PK-PD… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …product(s) or clinical studies to review and revise CSPs, ICFs, Clinical Study Reports (CSRs), and build and review Statistical Analysis Plans (SAPs) and ... development of minimum core product safety requirements for inclusion in Clinical study protocols (CSPs) and Informed Consent Forms (ICFs), for assigned… more
- Merck & Co. (Rahway, NJ)
- … Clinical Development Finance Under the guidance of the Oncology Clinical Development Finance Associate Director, the Finance Senior Specialist will:Provide ... and analytical support to our Research & Development Division Oncology Clinical DevelopmentForecast grant spend as well as provide financial support related… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …disorders. Summary The incumbent will be responsible for ensuring the delivery execution of clinical studies in one or more geographic regions, in adherence to ... and International Conference on Harmonization (ICH) guidelines. The Senior Clinical Study Manager will have routine interaction... Study Manager role is primarily a tactical study delivery role, reporting into an Associate … more
- Merck & Co. (Rahway, NJ)
- …Respiratory projects, including pipeline candidates and licensed productsSupervises development of clinical documents including protocols, clinical study ... Job DescriptionThe Associate Vice President (AVP)/Section Head, Global Clinical Development, Respiratory will focus on driving strategy, development, and… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- … Associates (SAs) or Senior SAs who assist in planning and in the execution of clinical studies in adherence to the protocol, Good Clinical Practices (GCPs), ... and provide this feedback through regularly scheduled 1:1 meetingsCollaborate with Clinical Study Manager on SA deliverablesParticipates in departmental and… more
- Lane County (Eugene, OR)
- …persistent mental health needs. This position requires a QMHP certification or registration as a clinical associate . If you are driven to serve, this is the job ... Certification NPI DiplomaCV or ResumeFor MHS1 - QMHP Certification or enrolled as Clinical Social Work Associate , Licensed Professional Counselor Associate … more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …Functional Expertise:Serves as a subject matter expert in medical codingReviews/approves clinical study related documents pertaining to medical coding and ... Position manages the end-to-end delivery of medical coding data for assigned projects/ studies collaborating with clinical and medical teams, CROs and other… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- About the Department The Clinical , Medical and Regulatory (CMR) department at Novo Nordisk is one of the most diverse and collaborative groups within the ... a living. Are you ready to make a difference? The Position The Associate Director, Research Partnerships (RP) is responsible for developing and executing Real-World… more
- Lane County (Eugene, OR)
- …QMHP CertificationNPIDiplomaCV or ResumeFor MHS1 - QMHP Certification or enrolled as Clinical Social Work Associate , Licensed Professional Counselor Associate ... peer support specialists, case managers, nurse practitioner, office assistant, and a clinical supervisor. For this recruitment we are looking for individuals with a… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …- Responsible, with limited supervision, for study activities assigned, eg for a clinical study : provide input on the development of study protocol ... The position will act as main statistical contact for the assigned studies , in particular in cross-functional Study team(s).Responsibilities- Study … more
- Lane County (Eugene, OR)
- …CertificationNPIDiplomaCV or Resume For MHS1 - QMHP Certification or enrolled as Clinical Social Work Associate , Licensed Professional Counselor Associate ... Associate For MHS2 - Oregon Health Licensure required: Licensed Clinical Social Worker, Licensed Professional Counselor, Licensed Psychologist or Licensed… more
- Lane County (Eugene, OR)
- …NPI Diploma CV or Resume For MHS1 - QMHP Certification or enrolled as Clinical Social Work Associate , Licensed Professional Counselor Associate or Licensed ... Associate For MHS2 - Oregon Health Licensure required: Licensed Clinical Social Worker, Licensed Professional Counselor, Licensed Psychologist or Licensed… more
- Eisai, Inc (Nutley, NJ)
- …If this is your profile, we want to hear from you. Summary The Associate Director is responsible for developing RWE strategies for assigned product(s) and execution ... of vendors selected to manage ongoing RWE efforts, including Ph4 study management, and presentations and publications emanating from these effortsActively… more
- Genmab (Remote, OR)
- …CTA/IND/HA regulatory submissions, plans required for the conduct of clinical studies , and clinical study data collection and results reporting. ... experience highly preferred. Extensive experience writing protocols, investigator's brochures, clinical study reports, Health Authority briefing packages, Health… more
Related Job Searches:
Associate,
Associate Clinical Study Manager,
Clinical,
Clinical Study,
Senior Clinical Study Associate,
Study,
Study Associate,
Temp Clinical Study Associate