Biotech Senior Director Clinical Operations Jobs

Currently, there are no Biotech Senior Director Clinical Operations jobs available which match this search. You may wish to explore similar job titles on the Biotech jobs page or view related jobs below.
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Description CSC has an immediate position for an Associate Director, Regulatory Operations. The qualified candidate performs critical review of regulatory documents for writing standards, logic, content, presentation and clarity. This position is located in Frederick, Maryland. Essential Job Functions Performs critical review of regulatory documents for writing standards, logic, content, presen...
WHO WE ARE Bio-Techne is a global life sciences company providing innovative bioactive tools and resources for the research and clinical diagnostic communities. The Company’s products assist scientific investigations into biological processes and the nature and progress of specific diseases. They aid in drug discovery efforts and provide the means for accurate clinical tests and diagnoses. With o...
*This position is home-based. We prefer someone near a major hub* DOCS is seeking a Senior Director of Global Program Management to provide leadership for, and oversight of, DOCS’ evolving portfolio of FSP and Resourcing Programs. This is a fantastic opportunity to drive excellence in Program Management with a leading provider of Resourcing Solutions to the Clinical Trials Industry. The Role a...
*This position is home-based. We prefer someone near a major hub* DOCS is seeking a Senior Director of Global Program Management to provide leadership for, and oversight of, DOCS’ evolving portfolio of FSP and Resourcing Programs. This is a fantastic opportunity to drive excellence in Program Management with a leading provider of Resourcing Solutions to the Clinical Trials Industry. The Role a...
Description CSC has an immediate position for a Director, Regulatory Affairs, to support Dynport Vaccine Company (DVC). The qualified candidate will manage the day to day operations of the Regulatory Affairs and Regulatory Operations groups and will be responsible for implementing the strategic direction set by the Senior Director. This position is located in Frederick, Maryland. Essential Job F...
The Senior Manager/Associate Director, Clinical Trial Supply Management will work as an integral member of Jazz Pharmaceuticals’ team, assisting in the development of new products. The Senior Manager/Associate Director, Clinical Trial Supply Management will manage clinical trial supplies in support of the development pipeline and other clinical and non-clinical studies. May also provide general CM...
WHO WE ARE Bio-Techne is a global life sciences company providing innovative bioactive tools and resources for the research and clinical diagnostic communities. The Company’s products assist scientific investigations into biological processes and the nature and progress of specific diseases. They aid in drug discovery efforts and provide the means for accurate clinical tests and diagnoses. With o...
Description CSC has an immediate opening for a Regulatory Affairs Manager. The Regulatory Affairs (RA) Manager develops regulatory filing strategies in support of domestic and international filing initiatives. This position is located in Frederick, Maryland. Essential Job Functions Serves as the DVC RA representative on multiple product teams and committees, interfaces with appropriate internal...
Personify Cambridge, MA
The Company: We represent a privately held global clinical research organization servicing the pharma, biotech, and device industries on an exclusive search assignment. Their drug and device development services allow them to offer a full service solution in every phase of clinical development. With multiple therapeutic specialties, they combine trial management, regulatory consulting, and innovat...
Job Description : PAREXEL currently has excellent opportunities for Project Leaders / Senior Project Leaders ( Project Managers) and Project Directors with a background in leading clinical trials ( Phase II and III) in a variety of therapeutic areas including; Oncology, Diabetes, CNS, Infectious Disease and Lupus. These positions can be office or regionally home based. The individuals selected fo...
Job Description : PAREXEL currently has excellent opportunities for Project Leaders / Senior Project Leaders ( Project Managers) and Project Directors with a background in leading Clinical trials ( Phase II - IV) in a variety of therapeutic areas including; Oncology, Diabetes, CNS, Infectious Disease, Cardio, Respiratory and Lupus. These positions can be office or regionally home based. The indiv...
Takeda Pharmaceuticals North America Boston, MA, 02298
Please note that the requirements specified in this posting are the basic qualifications required for the Sr. Director position; however, job title will be dependent on the candidate's level of experience in those requirements. Takeda has contributed significantly to the global pharmaceutical effort to help patients with gastrointestinal (GI) disease and is committed to becoming the world leader ...
The Sr. Manager, Clinical Operations is responsible for the clinical project management of assigned clinical study(ies) . The Sr. Manager partners with the Study Execution Team (SET) Lead and the cross-functional SET to ensure adherence to Onyx SOPs, GCP/ICH, and study specific procedures is followed and that the project scope, schedule and resources are managed appropriately. Participates in acti...
TechData is hiring for Associate Director of Biostatistics (Prefer Bayesian adaptive designs),SAS/Statistical Programmer(Some positions can be telecommuting), Biostatistician(Some can be telecommuting), Medical Writer, Regulatory Documentation Specialist, Senior Publishing Specialist, Sr. Clinical Supply Manager, Sr. Clinical Data Manager for our pharmaceutical clients in Northern NJ. We also have...
Personify Cambridge, MA
The Company: We represent a privately held global clinical research organization servicing the pharma, biotech, and device industries on an exclusive search assignment. Their drug and device development services allow them to offer a full service solution in every phase of clinical development. With multiple therapeutic specialties, they combine trial management, regulatory consulting, and innovat...
Hirenexus Cambridge, MA
The Company:We represent a privately held global clinical research organization servicing the pharma, biotech, and device industries on an exclusive search assignment. Their drug and device development services allow them to offer a full service solution in every phase of clinical development. With multiple therapeutic specialties, they combine trial management, regulatory consulting, and innovati...
Personify Boston, MA
The Company: We represent a privately held global clinical research organization servicing the pharma, biotech, and device industries on an exclusive search assignment. Their drug and device development services allow them to offer a full service solution in every phase of clinical development. With multiple therapeutic specialties, they combine trial management, regulatory consulting, and innovat...
TypeRegular Full-Time Job Code*LI-AB1 Overview: Mallinckrodt Pharmaceuticals is pleased to bring Questcor and its entire business into our company. The former Questcor organization will be known as the Autoimmune and Rare Diseases business within Mallinckrodt’s Specialty Pharmaceuticals segment. We will continue their focus on the treatment of patients with serious, difficult-to-treat autoimmu...
The Clinical Development Services division of Quintiles has more depth of therapeutic expertise and a broader range of services than any other service provider. We conduct both US and Global trials in all therapeutic areas. In fact, Quintiles conducts more clinical trials than anyone else in the world. Become involved in work that improves the quality of life for people around the globe. Let your ...
TechData is looking for Biostatistician (some can be telecommuting), SAS Programmer/Statistical Programmer (Some can be telecommuting), Recruiter, Project manager, Quality Assurance, Database Administrator, Drug Safety Specialist, Clinical Data Managerfor our pharmaceutical clients in Central NJ. Please see below requirements and send your resume to: *****. TechData is a l...

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