Clinical Affairs Associate Manager Jobs

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22 Clinical Affairs Associate Manager jobs found on Monster.

Jobs 1 to 20 of 22
Our client is looking for a Manager or Associate Director of Regulatory Affairs with solid regulatory affairs management experience from the biopharmaceutical industry. Specifically, we are looking for someone who is able to handle the following responsibilities. 1) Manage the preparation and submission of regulatory filings to FDA and other regulatory authorities 2) Ensure that regulatory project...
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...
Our client, a pharmaceutical company, is seeking a Sr. Regulatory Affairs Associate till the end of the year. The pay rate is up to $74 an hour plus benefits. The Sr. Regulatory Affairs Associate will be responsible for: • Advise stakeholders of submission completion. • Find information and potential answers to challenging areas related to assigned projects in the interest of keeping the project s...
Company: Yoh Associate Director, Regulatory Affairs Advertising and Promotion needed for a contract opportunity with Yoh's client located in Warren, NJ. The Big Picture - Top Skills You Should Possess: - Regulatory Affairs - Advertising and Promotion What You'll Be Doing: - Manage regulatory aspects of Post-Marketing regulatory submissions and communications with the Food and Drug Administration (...
Company: Yoh Regulatory Affairs Manager needed for a contract opportunity with Yoh's client located in Thousand Oaks, CA. The Big Picture - Top Skills You Should Possess: - Support one or more products from a regional regulatory perspective. As a member of the Global Regulatory Team (GRT), they will achieve the desired labeling by developing and executing regional regulatory strategies - Advising...
Job Responsibilities Under general supervision from the Clinical Operations Associate Director, management of operational aspects of the clinical trial by supporting development of the protocol synopsis; feasibility questionnaire and assessments; site initiation; co-monitoring; management of a full service CRO, vendors, and/or contract monitors through data-base closure; Final CSR; and publication...
Note: Candidates must possess Ph. 1 and 2 Full Service Oncology PM Experience -SUMMARY: The Clinical Operations Senior Project Manager (SPM) is responsible for overall management of all phases of clinical trials, from start-up through completion of activities, utilizing MedSource or sponsor Standard Operating Procedures (as applicable), FDA regulations, and ICH-GCP guidelines. In-depth knowledge a...
Note: Candidates must possess Ph. 1 and 2 Full Service Oncology PM Experience -SUMMARY: The Clinical Operations Senior Project Manager (SPM) is responsible for overall management of all phases of clinical trials, from start-up through completion of activities, utilizing MedSource or sponsor Standard Operating Procedures (as applicable), FDA regulations, and ICH-GCP guidelines. In-depth knowledge a...
Description Job Summary: The Clinical and Exploratory Pharmacology (CEP) Clinical Trial Manager (CTM) is responsible for the overall operational planning and activities for the implementation and conduct of clinical exploratory pharmacology clinical trials in compliance with ICH, GCP’s, SOPs, local requirements, internal/departmental guidelines, and established timelines. The CTM is involved in th...
Job Description: The purpose of this group is to provide strategic direction for product and disease communications and activities by interpreting current FDA regulatory environment to ensure truthful and non-misleading communication to health care community, patients, and the public. This position is primarily responsible to formulate and communicate the regulatory promotional position for approv...
The Director of Clinical Management and Long Term Services and Supports ensures compliance with the Centers for Medicare and Medicaid (CMS) and the State of Massachusetts clinical requirements for care management, care coordination, and utilization management for dually eligible beneficiaries. Provider leadership and for all care management activities and referral functions, including clinical pop...
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...
Successful candidates will be AstraZeneca Employees and will be located at AstraZeneca's MedImmune strategic science center in Gaithersburg, Maryland. MedImmune is the worldwide biologics research and development arm of AstraZeneca, a global, innovation-driven biopharmaceutical business that focuses on the discovery, development and commercialization of small molecule and biologic prescription med...
Type Regular Full-Time Job Code *LI-AB1 Overview: Questcor Pharmaceuticals, Inc. is a specialty biopharmaceutical company which provides products for patients with serious, difficult-to-treat autoimmune and inflammatory disorders. We support research in a number of rare conditions, including in treatment-resistant patient populations, in which there is significant need for improved therapeutic opt...
Type Regular Full-Time Job Code *LI-AB1 Overview: Questcor Pharmaceuticals, Inc. is a specialty biopharmaceutical company which provides products for patients with serious, difficult-to-treat autoimmune and inflammatory disorders. We support research in a number of rare conditions, including in treatment-resistant patient populations, in which there is significant need for improved therapeutic opt...
Health Net, Inc. is a publicly traded managed care organization that delivers managed health care services through health plans and government-sponsored managed care plans. Its mission is to help people be healthy, secure and comfortable. Health Net, through its subsidiaries, provides and administers health benefits to approximately 5.4 million individuals across the country through group, individ...
Are you looking for a Clinical Research position with a large pharmaceutical company Maryland, Northern NJ and PA areas. TechData Service has multiple positions in Pharmaceutical companies in clinical research, Medical Writing, Electronic Submissions, Technical Writer, Manufacturing Tech., Accounts Payable Clerk and Biostatistics/SAS Programming positions (both home based and work on site). We can...
Are you looking for a Clinical Research position with a large pharmaceutical company Maryland, Northern NJ and PA areas. TechData Service has multiple positions in Pharmaceutical companies in clinical research, Medical Writing, Electronic Submissions, Technical Writer, Manufacturing Tech., Accounts Payable Clerk and Biostatistics/SAS Programming positions (both home based and work on site). We can...
Safety Medical Writer- Manage the production of aggregate reports for assigned products (small to medium complexity reports) including planning, conducting meetings, writing, coordination of production and modification, assembly in documentum and addressing questions. Perform quality reviews for AR peer reports. PRINCIPAL RESPONSIBILITIES: List major responsibilities and duties of the position. Li...
QUALIFICATIONS Must have current CA R.N. license with a minimum of four years management/supervisory experience and continued education in the psychiatric field, or Bachelors degree in nursing with two years experience, or Masters degree in nursing with one year experience in the psychiatric field. Current BCLS for Healthcare Providers and ACLS required upon hire; MAB and LPS designation required...
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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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