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Clinical Research Associate Director Jobs

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533124true533124falseSubmission for the position: Clinical Research Associate II Regulatory - Calrg Clinical Research ( Full Time - Days ) - (Job Number: 90888)false533124falsetruehttps://swedish.taleo.net/careersection/jobdetail.ftl?job=90888&lang=enClinical Research Associate II Regulatory - Calrg Clinical Research ( Full Time - Days )trueClinical Research Associate II Regulatory - Calrg Clinica...

Johnson & Johnson companies are equal opportunity employers. Senior Clinical Research Scientist (Senior Clinical Research Associate)-3898150716 Description The Cardiovascular and Specialty Solutions (CSS) group, within the Johnson & Johnson's Family of Companies, is recruiting for a Senior Clinical Research Scientist, located in Irvine, CA. This position may require occasional travel to Menlo P...

Please note that the requirements specified in this posting are the basic qualifications required for the Associate Director, Global Outcomes Research position; however, job title will be dependent on the candidate's level of experience in those requirements. OBJECTIVES: This position functions within Takeda’s Global Outcomes Research (GOR) team, which contributes to the successful development a...

Please note that the requirements specified in this posting are the basic qualifications required for the Associate Director, Global Outcomes Research position; however, job title will be dependent on the candidate's level of experience in those requirements. OBJECTIVES: This position functions within Takeda’s Global Outcomes Research (GOR) team, which contributes to the successful development a...

ASSOCIATE DIRECTOR, CLINICAL RESEARCH REQUIREMENT #15-01096 RECRUITER: ANNIE DOYLE JOB LOCATION: JERSEY CITY, NJ AUGUST 4, 2015 *** CANDIDATES MUST BE ABLE TO WORK ON OUR PAYROLL AS A W-2 *** Project Description: Serve as a Clinical Lead at the study level and as the single point of accountability for clinical strategy, design, review, clinical oversight, and reporting of a clinical study or...

Description Contribution in selection and support BMS Immunoscience discovery portfolio, supervise and direct the transition of selected compounds into early clinical studies • Design, authoring and execution of proof-of-concept research plans and protocols that meet ethical, scientific, safety, regulatory and commercial objectives. • Review and Interpret clinical data supporting and guiding ap...

Overview: Why Join Us? Ultragenyx is a clinical stage biotechnology company committed to bringing to market novel products for the treatment of rare and ultra-rare diseases with an initial focus on serious debilitating metabolic genetic diseases. Founded in 2010, the company has rapidly built a diverse portfolio of both large and small molecule candidates with the potential to address diseases f...

As a member of the Clinical Research and Development group within the Clinical Development organization, the Medical Director will be responsible for providing medical subject matter expertise to support a regulatory filing for neratinib in breast cancer, and duties may include data analysis and interpretation; writing and reviewing components of the Common Technical Document (CTD); interactions w...

Title: Associate Director, Clinical Research Knowledge of Women s health and Urology therapeutic experience Preferred. Must have Clinical Development experience in the pharmaceutical sector. Serve as a Clinical Lead at the study level and as the single point of accountability for clinical strategy, design, review, clinical oversight, and reporting of a clinical study or group of studies within ...

Position Summary: The Associate Director of Clinical Data Management overseeing the Oncology Therapeutic area has shared accountability for delivering clinical research data management leadership for one or more clinical operation hubs, resulting in high quality, high value and timely clinical trial data that enable data exploration and analysis to drive informed portfolio decisions. The individua...

Requirements: - MD, PhD or PharmD preferred -Clinical development experience in a pharmaceutical setting is a must -Experience in running studies a must (writing protocols a key piece) -For advanced degree: 5+years’ work experience with at least 3 years in pharmaceutical drug development; or equivalent experience in academic or biotech sectors in the preferred Therapeutic Area (Women’s Health ...

Requirements: MD, PhD or PharmD preferred For advanced degree: 5+years’ work experience with at least 3 years in pharmaceutical drug development; or equivalent experience in academic or biotech sectors in the preferred Therapeutic Area (Women’s Health and Urology) or a closely related one. For BA: 7+years’ work experience with at least 5 years in pharmaceutical drug development; or equivalent e...

We have a permanent opening for a Cardiovascular MD - Clinical Research Physician at the Associate Medical Director level. The position is tactical in nature and responsible for Physician study level activities including for clinical study design, medical monitoring, clinical data review/analysis, etc. for clinical studies in phases I-III. Our client is an industry leading, publicly traded pharm...

Associate Director, Clinical Research Physician - ONCOLOGY-5238150731 Description Janssen Research and Development, L.L.C., a member of Johnson & Johnson's Family of Companies, with a specific focus on the field of Oncology, is recruiting for an Associate Director Clinical Research, Oncology, located in Spring House, PA or Raritan, NJ. At the Janssen Pharmaceutical Companies of Johnson & Johnso...

Description Contribution in selection and support BMS Immunoscience discovery portfolio, supervise and direct the transition of selected compounds into early clinical studies • Design, authoring and execution of proof-of-concept research plans and protocols that meet ethical, scientific, safety, regulatory and commercial objectives. • Review and Interpret clinical data supporting and guiding ap...

Company Overview Relypsa, Inc. is a late clinical-stage pharmaceutical company leading the discovery and development of novel non-absorbed polymeric drugs for important applications in cardiovascular and renal diseases. Relypsa's lead product candidate is patiromer, a non-absorbed potassium binder, which is being developed for the treatment of hyperkalemia. The company was formed in 2007 and is b...

* Provide expertise in clinical HIV medicine across multiple functions * Review and design protocols * Evaluate safety and efficacy data * Analyze and summarize data for internal and external audiences * Provide assistance and support in managing relationships with regulatory affairs, biometrics, clinical pharmacology, clinical virology and other departments within Gilead * Provide support for the...

Position Summary: The Associate Director of Clinical Data Management overseeing the Oncology Therapeutic area has shared accountability for delivering clinical research data management leadership for one or more clinical operation hubs, resulting in high quality, high value and timely clinical trial data that enable data exploration and analysis to drive informed portfolio decisions. The individu...

The prospective candidate leads development/validation/implementation of image analysis algorithms to enable use of clinical imaging endpoints in Biogen Idec clinical trials for decision-making. The candidate provides expert consultancy on appropriate application of clinical imaging endpoints in the design of clinical trials. Will use internal and external expertise/resources, contractors and key...

The Associate Medical Director is responsible for working with Medical Writing, Clinical Operations, Project Management and R& D to design, prepare and execute clinical protocols for early phase drug development candidates in the Acorda pipeline. This individual collaborates extensively with Clinical colleagues, regulatory affairs, and the commercial organization. The Associate Medical Director le...