Clinical Affairs Associate Manager Jobs

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34 Clinical Affairs Associate Manager jobs found on Monster.

Jobs 1 to 20 of 34
Our biopharmaceutical client is experiencing a growth in business creating the need to fill a Senior Regulatory Affairs Associate/Manager position. The company has a robust clinical pipeline, and now would be an exciting time to get involved in the growth. This would be an ideal position for a Senior Regulatory Associate looking to take their career to the next level. A competitive salary and bene...
TRG has recently been engaged by one of our top clients located in New Jersey, a rapidly growing and respected Pharmaceutical organization that is actively seeking qualified candidates for the role of REGULATORY AFFAIRS ASSOCIATE to help them with the development of their cutting edge portfolio of pharmaceuticals. ADVANTAGES OF THIS OPPORTUNITY: CHANCE TO MAKE A DIFFERENCE – As the newest vital me...
Our major pharmaceutical client is looking for a Regulatory Affairs Manager II in Thousand Oaks, CA for a 12 month contract job. Job description To ensure that the client acquires and maintains all the required licenses in order to support clinical trials for investigational medicinal products as well as market commercially approved medicinal products . Job responsibilities • Plans and manages reg...
Nature and Scope The Regulatory Associate provides administrative support to the Clinical Regulatory group. He/She is responsible for the organization and compilation of the regulatory submissions and maintains the regulatory files to ensure that dossiers are easily retrieved for review by the team. He/She works with pharmacovigilance to process and file Pharmacovigilance reports to the FDA in a t...
The RA Biosimilars Team is responsible for generation and implementation of the global regulatory strategies and the development and implementation of regulatory plans for CTA, CTD and related agency submissions for biosimilar products. JOB SUMMARY: Contribute to the development of, and lead the implementation of, regulatory strategies that result in the execution of regulatory plans for meeting i...
Clinical Research Manager II – 6 month contract Support US efforts in the planning, execution and reporting of US Clinical Data and Medical Affairs (CDMA) clinical trials in Oncology: Implementation of clinical trials in the United States (safety, data consistency, trial timelines, budget, resources, eligibility and enrollment), within a cross functional team and with oversight from the Associate...
TechData is looking for Biostatistician (Contract/permanent, or remote), SAS Programmer/Statistical Programmer (Some can be telecommuting), Task Based Clinical Data Coordinator/Clinical Data Manager, CRS (Clinical Research Scientist, Clinical Scientist), Clinical Safety Scientist/Drug Safety for our pharmaceutical clients in Northern and Central NJ. Please see below requirements and send your resu...
Requirements: - BS in Biology or Healthcare field - 1 year experience in Drug Development, Regulatory Affairs, CRA experience a plus. - Dialysis, Rheumatology, Oncology, Cardiology, Pediatrics or GI experience preferred - Ability to travel up to 80%, including overnight - Knowledge of Medical/Regulatory Terminology Description: - Assist with Administration of clinical research projects: recruiting...
Overview The primary responsibility of the Sr.CPM is to oversee and manage global trials for all clinical phases, in partnership with other functions and the Regional Clinical Trial Managers (RCTMs). The Sr.RCTM is also responsible to provide professional expertise and leadership through leading global departmental tasks, taking initiatives in improving GCO processes and providing mentoring, train...
Job Title: Clinical Research Manager II (3915584) Location: East Hanover, NJ Duration: 6 Months Company: Artech Information Systems LLC. Client: A Leading Pharmaceutical Organization Job Description Support US efforts in the planning, execution and reporting of USCDMA clinical trials in Oncology. Major Responsibility: 1.Implementation of clinical trials in the United States (safety, data consisten...
Our client is currently seeking a CONTRACTOR, CLINICAL DATA MANAGEMENT. This is a W2 contract opportunity in Northern NJ with a dynamic, growing pharmaceutical firm. Must have strong Clinical Data experience as well as CRO/Vendor management and proven ability to work with cross-functinal teams. Please send your resume as a Word document for immediate consideration to ***** The Contractor,...
Clinical Research Manager II w2 candidates only 6 month, renewable contract Duties Support US efforts in the planning, execution and reporting of USCDMA clinical trials in Oncology. 1.Implementation of clinical trials in the United States (safety, data consistency, trial timelines, budget, resources, eligibility and enrollment), within a cross functional team and with oversight from the Associate...
Minimum Requirements: Prior experience with Implementation of clinical trials in the United States safety, data consistency, trial timelines, budget, resources, eligibility and enrollment. Education: Bachelor Degree required Job Description: Support US efforts in the planning, execution and reporting of USCDMA clinical trials in Oncology. Implementation of clinical trials in the United States (saf...
Manager, Senior Manager or Associate Director, Biostatistics Several openings with 3 different clients North NJ Pharmaceutical/Biotechnology Base Salary: Minimum: $120,000 to $150,000 base plus bonus, benefits (relocation available if qualified) Description: .Provide statistical input to Medical Affairs teams for the .design, planning and conduct of analyses of Phase IV clinical trials and .observ...
EXPAND YOUR MEDICAL INFORMATION CAREER At APCER Pharma Solutions, Inc. we have an opportunity for you to expand your scope of skills and responsibilities at our growing and evolving company. We are looking for an experienced Senior Manager/Associate Director of Medical Information Services who brings technical acumen, the ability to build and lead a team through rapid growth, and a work style that...
MEDICAL PROGRAM ASSISTANT ASSOCIATE UNIVERSITY OF WISCONSIN - MILWAUKEE NORRIS HEALTH CENTER POSITION ANNOUNCEMENT MEDICAL PROGRAM ASSISTANT ASSOCIATE Official Job Title: MEDICAL PROGRAM ASSISTANT ASSOCIATE Working Title: Appointment Type: Classified Permanent Department: B0350 STUDENT HEALTH SERVICES Title Code: 23002 Job Number 02085994/02085996 Posting Type: Civil Service Positions Open for Tra...
Title Associate Director Scientific Training - Respiratory Description Description: The Associate Director Scientific Training - Respiratory (ADST-Respiratory) is responsible for leading the scientific content development and training for Medical Affairs activities in support of the respiratory therapeutic area and medical brand plan objectives. The ADST partners with the respiratory Learning & De...
Description The Associate Director Scientific Training - Oncology (ADST-Oncology) is responsible for leading the scientific content development and training for Medical Affairs activities in support of the oncology therapeutic area and medical brand plan objectives. The ADST partners with the oncology Learning & Development Manager to develop appropriate content and learning approaches to efficien...
Description The Associate Director Scientific Training - ID/RIA (ADST-ID/RIA) is responsible for leading the scientific content development and training for Medical Affairs activities in support of the ID/RIA therapeutic areas and medical brand plan objectives. The ADST partners with the ID/RIA Learning & Development Manager to develop appropriate content and learning approaches to efficiently and...
Johnson & Johnson companies are equal opportunity employers. Associate Director, Consumer Surveillance and Signal Detection-0548140203 Description Johnson & Johnson Consumer Products Company, a division of Johnson & Johnson Consumer Companies, Inc., is recruiting for an Associate Director, Consumer Surveillance and Signal Detection, in Horsham, PA. Johnson & Johnson Consumer Products Company, a di...
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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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