Regional Clinical Research Associate Jobs

RSS

1000+ Regional Clinical Research Associate jobs found on Monster.

Jobs 1 to 20 of 1650
Title of Position: Clinical Research Associate/Regional Monitor Minimum Requirements: CRA WITH ONCOLOGY/HEMATOLOGY BS REQUIRED Essential skills needed for assignment: Minimum BA/BS preferably in health/medical related field or life sciences area • Must have a minimum of 5 years experience Must have 2 years min oncology/hematology clinical trials experience • Strong computer skills are esse...
Job Description : JOB DESCRIPTION Job Title Senior Clinical Research Associate (CRA), EPD Department EPD (Clinical Operations) SBU Early Phase Essential Function Performs clinical monitoring and investigational site /relationship management for designated EPD led clinical trials in accordance with ICH GCP, applicable regulations and SOPs. Act as PAREXELs direct contact with sites and is resp...
Job Description : JOB DESCRIPTION Job Title Senior Clinical Research Associate (CRA), EPD Department EPD (Clinical Operations) SBU Early Phase Essential Function Performs clinical monitoring and investigational site /relationship management for designated EPD led clinical trials in accordance with ICH GCP, applicable regulations and SOPs. Act as PAREXELs direct contact with sites and is resp...
Are you passionate about improving the quality of human life? If so, we invite you to learn more about our home-based CRAs opportunities for Phases I-IV in the U.S. and Canada. ICON Clinical Research has a strong reputation in our approaches to clinical development. We apply scientific and operational excellence across all phases of clinical trial outsourcing services for our clients. We work wit...
Are you passionate about improving the quality of human life? If so, we invite you to learn more about our home-based CRAs opportunities for Phases I-IV in the U.S. and Canada. ICON Clinical Research has a strong reputation in our approaches to clinical development. We apply scientific and operational excellence across all phases of clinical trial outsourcing services for our clients. We work wit...
Founded in 1982 out of a start-up on the University of North Carolina, USA, campus, Quintiles Inc. has forged the idea of helping pharmaceutical companies conduct objective clinical trials to establish whether a drug is effective and safe. As the largest provider of pharmaceutical development services, we have helped develop all of the top 50 best-selling drugs on the market. We have a network of ...
Job Description : JOB DESCRIPTION Job Title Senior Clinical Research Associate (CRA), EPD Department EPD (Clinical Operations) SBU Early Phase Essential Function Performs clinical monitoring and investigational site /relationship management for designated EPD led clinical trials in accordance with ICH GCP, applicable regulations and SOPs. Act as PAREXELs direct contact with sites and is resp...
inVentiv Health -Transforming Promising Ideas into Commercial Reality We are currently hiring new Regional CRAs and Sr CRAs to work directly with one sponsor. You will be dedicated to their studies and be a permanent employee with full benefit package options, 401k, PTO and bonus potential. Job Title: Clinical Research Associate II or Sr Clinical Research Associate Primary Function: The posit...
Inventiv Health Clinical San Francisco, CA
Job Description: Monitor (pre-study, initiation, routine, and close-out visits) at investigator sites (60% travel with 75% at peak times) for GCP compliance according to inVentiv Health Clinical SOPs and/or client guidelines Recruit investigators for participation in clinical trials Negotiate study budgets with investigators Obtain, review for appropriateness, and process regulatory and admini...
Job Description: Monitor (pre-study, initiation, routine, and close-out visits) at investigator sites (60% travel with 75% at peak times) for GCP compliance according to inVentiv Health Clinical SOPs and/or client guidelines Recruit investigators for participation in clinical trials Negotiate study budgets with investigators Obtain, review for appropriateness, and process regulatory and admini...
Job Description: Monitor (pre-study, initiation, routine, and close-out visits) at investigator sites (60% travel with 75% at peak times) for GCP compliance according to inVentiv Health Clinical SOPs and/or client guidelines Recruit investigators for participation in clinical trials Negotiate study budgets with investigators Obtain, review for appropriateness, and process regulatory and admini...
Planet Pharma Minneapolis, MN
Planet Pharma is working with a client to hire a Regional Clinical Research Associate. You must have at least 5 years of monitoring experience, be home based in the Midwest US, and have experience in cardiac device. I will also look at candidates who have extensive cardio drug experience and device experience in another therapeutic area. However, this is a drug-stent study, so cardiac device exper...
DESCRIPTION Serves as primary contact point between the sponsor and the investigational site. A Site Manager is assigned to trial sites ensuring inspection readiness through compliance with the clinical research protocol, company's Standard Operating Procedures (SOP), codes of Good Clinical Practice (GCP), applicable regulations and guidelines from start-up through data-base lock. Responsibilitie...
Marten Transport San Francisco, CA
DESCRIPTION Serves as primary contact point between the sponsor and the investigational site. A Site Manager is assigned to trial sites ensuring inspection readiness through compliance with the clinical research protocol, company's Standard Operating Procedures (SOP), codes of Good Clinical Practice (GCP), applicable regulations and guidelines from start-up through data-base lock. Responsibilitie...
Marten Transport New York, NY
DESCRIPTION Serves as primary contact point between the sponsor and the investigational site. A Site Manager is assigned to trial sites ensuring inspection readiness through compliance with the clinical research protocol, company's Standard Operating Procedures (SOP), codes of Good Clinical Practice (GCP), applicable regulations and guidelines from start-up through data-base lock. Responsibilitie...
Marten Transport Beverly Hills, CA
DESCRIPTION Serves as primary contact point between the sponsor and the investigational site. A Site Manager is assigned to trial sites ensuring inspection readiness through compliance with the clinical research protocol, company's Standard Operating Procedures (SOP), codes of Good Clinical Practice (GCP), applicable regulations and guidelines from start-up through data-base lock. Responsibilitie...
Marten Transport Portland, OR
DESCRIPTION Serves as primary contact point between the sponsor and the investigational site. A Site Manager is assigned to trial sites ensuring inspection readiness through compliance with the clinical research protocol, company's Standard Operating Procedures (SOP), codes of Good Clinical Practice (GCP), applicable regulations and guidelines from start-up through data-base lock. Responsibilitie...
DESCRIPTION Serves as primary contact point between the sponsor and the investigational site. A Site Manager is assigned to trial sites ensuring inspection readiness through compliance with the clinical research protocol, company's Standard Operating Procedures (SOP), codes of Good Clinical Practice (GCP), applicable regulations and guidelines from start-up through data-base lock. Responsibilitie...
DESCRIPTION Serves as primary contact point between the sponsor and the investigational site. A Site Manager is assigned to trial sites ensuring inspection readiness through compliance with the clinical research protocol, company's Standard Operating Procedures (SOP), codes of Good Clinical Practice (GCP), applicable regulations and guidelines from start-up through data-base lock. Responsibilitie...
DESCRIPTION Serves as primary contact point between the sponsor and the investigational site. A Site Manager is assigned to trial sites ensuring inspection readiness through compliance with the clinical research protocol, company's Standard Operating Procedures (SOP), codes of Good Clinical Practice (GCP), applicable regulations and guidelines from start-up through data-base lock. Responsibilitie...

Get new jobs by email for this search
We'll keep looking and send you new jobs that match this search.
email me

Upload your resume and let employers find you!
It's that simple!

Healthcare Career Tools

Clinical Research Associate

Salaries

$32,614.00 - $97,000.00
Typical Salary for Clinical Research Associate
(340 Respondents)
Source: Monster.com Careerbenchmarking Tool

Education / Training

Bachelor's
48%
Master's
29.8%
Doctorate
12.4%
Associates
5.3%
(225 Respondents)
Source: Monster.com Careerbenchmarking Tool

Popular Regional Clinical Research Associate Articles

Work a Nursing Career Fair Article Rating
If you're attending such an event, read this advice on what to do before, during and after to land your job of choice.
Respiratory Therapists Help Ease Chronic Conditions Article Rating
Learn how respiratory therapists treat their patients and teach them how to breathe easier.
For Employers: Post Jobs | Search Resumes | Advertise
About Monster | Work for Monster | Advertise with Us | AdChoices | Partner with Us | Investor Relations | Social Media
Terms of Use | Privacy Center | Accessibility Center | Help | Security | Contact Us | Sitemap | Mobile
©2015 Monster - All Rights Reserved U.S. Patents No. 5,832,497; 7,599,930 B1; 7,827,125 and 7,836,060 MWW - Looking for Monster Cable? - V: 2015.1.0.4-321
eTrustLogo