Clinical Affairs Associate Manager Jobs

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As part of the iCAD/Xoft Clinical Affairs team, the Clinical Affairs Project Manager will be responsible for the coordination of all activities associated with the conduct of multiple clinical trials (develops study protocols, CRFs; supervises study tasks and mentors other CRAs; assists in the generation and oversight of trial budgets and contracts; and communicates trial status to management). In...
Director of Clinical Affairs Job Description The Director of Clinical Affairs is responsible for all U.S. and international clinical trials conducted by CapsoVision and assures compliance to all relevant local, national, and international regulations, guidelines, and ethical standards. The Director works closely with senior management to assess business objectivesand develop a clinical strategy ...
Our client is currently seeking a Clinical Manager - Medical Affairs. This is a 1 year contract (W2) opportunity in the Fort Worth area. For immediate consideration please send your resume as a Word or PDF file to *****. Will leadand manage the execution of a phase IIIb/IV program. Support Global BrandMedical Affairs; lead in planning and conducting clinical trials. This job will have th...
Our client is currently seeking a REGULATORY AFFAIRS MANAGER / SR. MANAGER. Opportunity to work in a dynamic environment and gain experience in Biologics! Contract opportunity in the Colonia , NJ area. For immediate consideration please send your resume to *****. Must be able to work as a W2 contractor directly for The Judge Group. The Senior Regulatory Manager handles a broad range of re...
VIVUS, Inc. Mountain View, CA
POSITION SUMMARY: We currently have a position open for a Senior Manager / Associate Director of Regulatory Affairs responsible for managing the activities surrounding clinical and CMC regulatory. Responsibilities include the preparation of document packages for regulatory submissions from all areas of the company. Other activities may include support of post-marketing commitments, ensure timely ...
Essential Responsibilities • Plan, implement and drive all aspects of clinical studies in compliance with GCP, (Good Clinical Practice,) the HAT (Human and Animal Trial Procedure,) Work Instructions, Corporate Policies, Guidelines and internal Standards. • Manage cross-functional team, facilitating the team's ability to fulfill their responsibilities in accordance with project specifications and...
Life-changers work here CareFusion Life-changers find innovative ways to improve our customers' ability to provide healthcare to their patients. One way is our search for bold and inspired employees across the globe. Are you ready to change lives? Join our 15,000 employees to help clinicians solve some of healthcare's most critical challenges. Meet one of our Life-changers. http://www.youtube.co...
Position Description: About Volcano We are revolutionizing the medical device industry with a broad suite of technologies that make imaging and therapy simpler, more informative and less invasive. Our products empower physicians around the world with a new generation of analytical tools that deliver more meaningful information - using sound and light as the guiding elements. Founded in cardiovasc...
Regulatory Affairs Manager – Perm Position in Greater Chicago Area Medical Device manufacturer has a need for an experienced Regulatory Affairs Manager. This position is responsible for managing various regulatory activities for their ventilator product line out of Finland business unit. This position will research, manage and support the maintenance for the Regulatory Compliance Plans and assoc...
Midwestern University Glendale, AZ, 85301
The Assistant/Associate Dean for Clinical Affairs will ensure the effective delivery of a high quality curriculum for the Doctor of Optometry degree. The position reports to the Dean, Arizona College of Optometry. Administration: A. Clinic Administration 1. Develop draft policies and procedures to enhance quality of patient care and efficiency of clinic operations. Process all draft policies fo...
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...
About Volcano We are revolutionizing the medical device industry with a broad suite of technologies that make imaging and therapy simpler, more informative and less invasive. Our products empower physicians around the world with a new generation of analytical tools that deliver more meaningful information - using sound and light as the guiding elements. Founded in cardiovascular care and expanding...
Our client is currently seeking a Clinical Manager - Medical Affairs. This is a 1 year contract (W2) opportunity in the Fort Worth area. For immediate consideration please send your resume as a Word or PDF file to *****. Will leadand manage the execution of a phase IIIb/IV program. Support Global BrandMedical Affairs; lead in planning and conducting clinical trials. This job will have th...
Siemens Corporation Berkeley, CA, 94705
Company Description Siemens Healthcare Diagnostics is a global leader in in vitro diagnostics, providing healthcare professionals in hospital, reference, and physician office laboratories and point-of-care settings with the vital information required to accurately diagnose, treat, and monitor patients throughout the continuum of care. We offer systems and solutions across a broad spectrum of disc...
Manager, Clinical Affairs Requisition ID -2528619432 The Position Actively participates on cross-functional project teams responsible for the development and commercialization of advanced staining and digital pathology products including, but not limited to antibodies, detection kits, molecular probes and image analysis applications. Fosters cross functional relationships to create a cooperati...
To facilitate product development and global registration by developing and executing regulatory strategies and effective regulatory agency interactions for product manufacturing and quality programs throughout product lifecycle. The RA CMC Regional Lead is responsible for generation of the region specific regulatory strategy and providing feedback to the team for plans and execution of the stra...
BRECKENRIDGE PHARMACEUTICAL, INC. REGULATORY AFFAIRS ASSOCIATE This position supports the Regulatory Affairs Manager in day to day activities to ensure the timely compilation and submission of ANDAs, Annual Reports, Periodic Reports, Amendments/Supplements, and Deficiency Letter Responses to the FDA. Location: CT Job Responsibilities Include: Review technical/regulatory/clinical documentation...
Hoffmann-La Roche Inc. Tucson, AZ, 85704
Manage activities associated with regulatory approval of in vitro diagnostic medical devices. Responsible for activities which lead to and maintain domestic and international regulatory approval to market devices. Responsible for assessment of device changes for regulatory implications. ESSENTIAL FUNCTIONS: Provide support to currently marketed products, e.g., review engineering changes, labelin...
Celgene is a global biopharmaceutical company leading the way in medical innovation to help patients live longer, better lives. Our purpose as a company is to discover and develop therapies that will change the course of human health. We value our passion for patients, quest for innovation, spirit of independence and love of challenge. With a presence in more than 70 countries - and growing - we l...
Description: We're changing the way health care works for the better. That means consulting with our members, partnering with our physicians, and delivering drugs in the most efficient and effective way. Join us and start doing your life's best work.(sm) The Manager, Regulatory Affairs has responsibility for managing strategic regulatory operations and providing expert advice on the guidelines a...

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Customer Service Career Tools

Clinical Affairs Associate Manager

Salaries

$41,600.00 - $165,000.00
Typical Salary for Clinical Affairs Associate Manager
(33 Respondents)
Source: Monster.com Careerbenchmarking Tool

Education / Training

Bachelor's
50%
Doctorate
31.2%
Master's
18.8%
(16 Respondents)
Source: Monster.com Careerbenchmarking Tool
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