Executive Director, Clinical Development - Oncology
At Daiichi Sankyo, we add to the Balance of Life through our commitment to science. With a century of R&D experience behind us, our Pharma Development organization offers a unique culture where everyone's contributions count. Executive Director, Clinical Development - Oncology Oversee and manage the global clinical ... more
Type: Full Time/Contract Location: Edison, NJ Country: United States Posted: 5/13/2008 6:31:48 PM
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Translational Medicine Clinician (Associate Director/Dir
Description: This person will be responsible for providing Translational Medicine support for multiple projects in oncology (at both preclinical and clinical stage) with an emphasis on the immunotherapy portion of the portfolio. Support will include designing and executing translational research plans and early clinical development plans, and design and ... more
Type: Full Time/Contract Location: La Jolla, CA Country: United States Posted: 5/13/2008 6:31:48 PM
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Dir, Clinical (M.D
Novartis is a world leader in offering medicines to protect health, cure disease and improve well-being. Our goal is to discover, develop and successfully market innovative products to treat patients, ease suffering and to enhance the quality of life. We also seek to provide a return to shareholders that reflects ... more
Type: Full Time/Contract Location: Cambridge, MA Country: United States Posted: 5/13/2008 6:31:44 PM
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Clinical Trial Associate Manager
Summary: Coordinates and implements clinical research projects and is involved with writing protocols and identifying, qualifying, and training clinical sites to conduct clinical trials. Oversees the collection of data to ensure compliance with protocol and the clinical research project objectives as well as FDA/ICH/GCP regulations and guidelines. Must be able ... more
Type: Full Time/Contract Location: Tarrytown, NY Country: United States Posted: 5/13/2008 6:31:43 PM
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Clinical Logistics Manager I
Purpose of Job: The Clinical Logistics Manager I (CLM I) elaborates and conducts logistics processes for clinical trials to the highest standards of quality and efficiency, ensuring that projects are conducted according to quality standards, including standard operating procedures, ICH, GCP, and GMP. Responsibilities: • Support for development of logistics ... more
Type: Full Time/Contract Location: Waltham, MA Country: United States Posted: 5/13/2008 6:31:43 PM
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Clinical Statistical Programmer
Description: POSITION PURPOSE: Role is primarily responsible for the project management of statistical programming actives in the Clinical Programming & Writing (CPW) group. SAS programming is a core skill, but main focus of the position is oversight of external providers performing programming. - Accountable for the provision of ... more
Type: Full Time/Contract Location: New London, CT Country: United States Posted: 5/13/2008 6:31:40 PM
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Clinical Pharmacology Lead, CVMED (Assoc Director/D4/Gr. 14
Description: As a member of cross-functional project teams, responsible for development and execution of clinical pharmacokinetic (PK)/pharmacodynamic (PD) plans, including drug-drug and drug-disease interaction strategies, that will optimize doses, dosage regimens and study designs throughout clinical drug development. Responsible for design, analysis, interpretation and reporting of PK and PD ... more
Type: Full Time/Contract Location: Groton, CT Country: United States Posted: 5/13/2008 6:31:40 PM
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Sr. Clinical Programmer
The Senior Clinical Programmer is responsible for performing the clinical systems activities for the entire life cycle of one or more clinical trials, from protocol concept review through completion of the Clinical Study Report (CSR). The position collaborates with the CDA, Stat Programmer and other members of the Study Management ... more
Type: Full Time/Contract Location: Cambridge, MA Country: United States Posted: 5/13/2008 6:31:40 PM
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Clinical Program Leader, Program Manager
Manages all aspects of an assigned clinical program or programs (globally) to ensure that all studies within the program are completed on time within budget and in compliance with SOPs, Regulatory regulations and ICH/GCP guidelines and in alignment with Therapeutic Area (TA) strategies and goals. Working with the MD and/or ... more
Type: Full Time/Contract Location: San Diego, CA Country: United States Posted: 5/13/2008 6:31:39 PM
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Clinical Research Associate
Zosano Pharma ™, Inc., formerly named The Macroflux Corporation, is a private specialty pharmaceutical company creating better products utilizing innovative drug delivery technology. Our company was founded in October 2006 upon a Johnson and Johnson Internal Ventures spin-out from the ALZA company. Based on a small patch and applicator, Zosano’s ... more
Type: Full Time/Contract Location: Fremont, CA Country: United States Posted: 5/13/2008 6:31:38 PM
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Clinical Statistical Programmer
Description: Position Purpose: Role is primarily responsible for the project management of statistical programming actives in the Clinical Programming & Writing (CPW) group supporting the Oncology Therapeutic Area for Phase IIIB/IV studies. SAS programming is a core skill, but main focus of the position is oversight of external providers ... more
Type: Full Time/Contract Location: New London, CT Country: United States Posted: 5/13/2008 6:31:38 PM
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Clinical Trials Specialist II
Job Summary: The Clinical Trials Specialist II role is to efficiently and expertly perform start up activities inclusive of site regulatory document collection, Clinical Study Agreement negotiations, and clinical document review services (review clinical investigator site regulatory package documents, and protocols as related to informed consent forms). The Clinical Trials ... more
Type: Full Time/Contract Location: Waltham, MA Country: United States Posted: 5/13/2008 6:31:37 PM
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VP of Medical Affairs
Vice President Medical Affairs Location: Emeryville, CA Position Type: Full time Required Education: MD degree required. Areas of Expertise: Experience in driving the adoption of new laboratory technology and information into clinical practice in US and Europe through design, development and execution of medical marketing programs. Reports to: Chief ... more
Type: Full Time/Contract Location: Emeryville, CA Country: United States Posted: 5/13/2008 6:31:37 PM
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Sr. Clinical Research Associate
ESSENTIAL FUNCTIONS · Strong monitoring skill set. · Train others in appropriate way to develop protocols and CRFs; review the work of others in such development. · Train others in how to prepare clinical sites for trial initiation and monitor clinical trials. · Manage ... more
Type: Full Time/Contract Location: South San Francisco, CA Country: United States Posted: 5/13/2008 6:31:36 PM
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STATISTICAL LEADER - PHARMA DEVELOPMENT
Located in the department of Biomathematics, you will provide high level statistical support to drug projects in the early phases of clinical development within one or several Disease Biology Areas. On project level teams you will engage in strategic discussions regarding the early clinical development of a compound even before ... more
Type: Full Time/Contract Location: Nutley, NJ Country: United States Posted: 5/13/2008 6:31:35 PM
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Clinical Data Manager
Under general supervision, the Clinical Data Manager reviews data; assists in database design and testing; designs CRFs and guidelines; designs and tests logic checks; generates queries for missing or discrepant data; utilizes tools/systems to code medical terms and medications; works with Clinical Monitoring, Medical Affairs, Database Development, Biometrics and Project ... more
Type: Full Time/Contract Location: Southborough, MA Country: United States Posted: 5/13/2008 6:31:34 PM
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Sr Regional Medical Liaison - Inflammation - NB50230461 - Nevada, California
This position is within the Inflammation RML therapeutic area. This postion will cover Nevada, Sacremento, San Bernardino and Riverside Counties of California. Identify, develop, and maintain collaborative relationships with current and future thought leaders. Work with thought leaders to develop clinical therapeutic concepts that support the advancement of the ... more
Type: Full Time/Contract Location: San Bernardino, CA Country: United States Posted: 5/13/2008 6:31:34 PM
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Clinical Trials Manager – Clinical Operations
Clinical Trials Manager – Clinical Operations Principal Duties and Responsibilities Assists in defining protocol(s) and develops informed consent forms, patient instruction guides, and reviews draft case report forms. Note: The Managers role will vary, depending on who is conducting the trial, i.e. in-house/outsourced, etc. The objective is ... more
Type: Full Time/Contract Location: Cambridge, MA Country: United States Posted: 5/13/2008 6:31:32 PM
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Associate Director/Clinical Scientist, Clinical Development
Job Title: Associate Director/Clinical Scientist, Clinical Development FLSA Status: Exempt Job Number: 01500308 Department: Clinical Development Description: The Associate Director of Clinical Development will be responsible for strategic clinical planning, clinical trial design, protocol development, evaluation and interpretation of clinical trial data, and presentation of clinical ... more
Type: Full Time/Contract Location: San Diego (Sorrento Valley), CA Country: United States Posted: 5/13/2008 6:31:30 PM
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Label Free/HTS Research Scientist (PhD
Novartis Institutes for BioMedical Research is Novartis' global research organization and is committed to discovering innovative medicines that cure disease and improve human health. By conducting more relevant and predictable drug discovery that can yield new and better medicines for patients, Novartis Institutes for BioMedical Research is redefining drug discovery ... more
Type: Full Time/Contract Location: Cambridge, MA Country: United States Posted: 5/13/2008 6:31:10 PM
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