Sr Clinical Research Associate Jobs

RSS

906 Sr Clinical Research Associate jobs found on Monster.

Jobs 1 to 20 of 906
Hologic, Inc. is a leading developer, manufacturer and supplier of premium molecular diagnostic products and services that are used to diagnose human diseases, screen donated human blood and to aid in biomedical research. Hologic is also a leader in the development, manufacturing and sales of medical imaging systems and biopsy devices as well as surgical and treatment products, with an emphasis on...
Location: Nationwide Responsible for implementing set-up, execution, oversight and reporting of clinical studies while ensuring that the conduct of the trial is in compliance with the protocol, ICH/GCP, and applicable regulatory requirements. Key Accountabilities/Core Job Responsibilities Lead multifunctional team through clinical studies activities that meet ICH/GCP and SOP requirements Devel...
CLINICAL RESEARCH COORDINATOR - ONCOLOGY Clinical Research Coordinator/RN needed for busy oncology practice in New Braunfels, Texas. Will be responsible for enlisting, maintaining, and assuring protocol compliance for all patients on clinical trials. Will collaborate with physicians in determining eligibility of patients for clinical trials, provide education for staff and patients and ensure sit...
We are seeking a Sr. CRA for a 6 plus month contract in either Sunnyvale or San Francisco. (Very Senior candidates would be allowed to work offsite with at least a two week orientation on site) Interested candidates should forward word doc resume with hourly salary requirements. Description Position Summary: Leads activities associated with the evaluation, initiation and management of clinical ...
Personify Raleigh, NC
The Company: Our client is an established, nationally recognized multi-specialty research site for the Pharmaceutical/Biotech and Clinical Research industry. They act as a division of 9 unified investigational sites with therapeutic indications such as Gastroenterology, Dermatology, Men/Women’s health, and Sleep to name a few. With over 20 successful years conducting phase I-IV trials and headq...
Job Description: POSITION SUMMARY: Under minimal supervision, work within the clinical research team in a field clinical monitoring role at clinical study sites to assure adherence to Good Clinical Practices (GCP), Standard Operating Procedures (SOPs), and study protocols. ESSENTIAL FUNCTIONS: • Monitor study sites for protocol, SOP and regulatory compliance • Ensure that monitoring reports a...
SUMMARY: Within the Global Medical Sciences group, independently manages from submission to study close out all activities related to the IST/CTEP Program. Works closely and independently with internal cross-functional IST Review Committee members, external collaboration partners, and external investigators, including key opinion leaders. Independently manages and facilitates the on-line activitie...
This is a home-based position in AL, AR, CI, DE, DC, FL, GA, KY, LA, ME, MD, MA, MS, NH, NJ, NY, NC, OH, PA, RI, SC, TN, VT, VA and WV. PPD - Local Community. Global Reach. Our global team of experienced CRA Managers work to ensure that our CRAs have an appropriate work load, the tools they need to be successful and that there is a plan for their continued career advancement. PPD CRAs also enjo...
Our Client in the East Bay Area is looking for a CRA II to join their Clinical team! Duties: - The CRA II evaluates and analyzes clinical data. - Work with Sr. CRAs to manage current clinical trials. - Maintains study documentation and analyzes data according to Company's SOPs. - The CRA II will help to develop SOPs, create/author CSRs, develop BIMO reports, and financial disclosure forms. -...
Essential Functions: Assist in supporting clinical operations management in the conduct of clinical studies to ensure studies are completed on time, within budget; and in compliance with SOPs, FDA regulations, and ICH/GCP guidelines Support the activities of planning, implementing, motivating, co-monitoring, and tracking clinical trials including review and development of case report forms, stud...
Kelly Services Plymouth Meeting, PA
Clinical Research Associate (CRA III / Sr. CRA) Our client, a Leading Pharma company is seeking a (CRA III / Sr. CRA) to join their team for a Global Study for a very Long Term Contract. The company has a robust clinical pipeline including an upcoming phase III study. There is tremendous opportunity to work with a collaborative group of scientists and professionals committed to bettering human l...
Personify Flushing, NY
The Company: Our client is an established, nationally recognized multi-specialty research site for the Pharmaceutical/Biotech and Clinical Research industry. They act as a division of 9 unified investigational sites with therapeutic indications such as Gastroenterology, Dermatology, Men/Women s health, and Sleep to name a few. With over 20 successful years conducting phase I-IV trials and headquar...
Ultimate Staffing Irvine, CA
This is your opportunity to work with a world leader!. Unlike your traditional Sr. CRA role, this job offers the opportunity for you to combine monitoring and clinical project management with the clinical specialist role into one position. As a senior CRA, you will be responsible for assisting in the development, management and close out of the clinical studies executed in conjunction with the Ad...
Kindred Healthcare Kansas City, MO
Schedule: Full-time Job ID: 150000EZ BRIEF DESCRIPTION: Monitors in accordance with ICH, GCP, CFR guidelines, UBC and project SOPs Essential Functions: Thorough knowledge and application of project specific protocol Consistently completes on site monitoring in accordance with project specific timelines Consistently completes travel scheduling in accordance with project specific and UBC guid...
Clinical Solutions Group Princeton, NJ
Mid-sized international pharmaceutical company has an immediate for a contract based Senior Clinical Research Associate. Periodic travel required as noted below. Selected candidate will be required to work out of the office when they’re not traveling. Top pay and benefits available. Initially forecasted for 1 year with the option to be extended. Position Summary: • Perform in-depth clinical revi...
Clinical Solutions Group Princeton, NJ
Mid-sized international pharmaceutical company has an immediate for a contract based Senior Clinical Research Associate. Periodic travel required as noted below. Selected candidate will be required to work out of the office when they’re not traveling. Top pay and benefits available. Initially forecasted for 1 year with the option to be extended. Position Summary: • Perform in-depth clinical revi...
DOCS Global is actively seeking Clinical Research Associates (CRAII), Regional, Lead, and Local Trial Managers in the Boston area who have primary therapeutic experience in Oncology and Cardiology as well as other therapeutic areas. Experience working with multiple protocols is required. Experience facilitating pre-study initiation process, orienting site personnel on protocols and procedures, com...
Personify Raleigh, NC
The Company: Our client is an established, nationally recognized multi-specialty research site for the Pharmaceutical/Biotech and Clinical Research industry. They act as a division of 9 unified investigational sites with therapeutic indications such as Gastroenterology, Dermatology, Men/Women’s health, and Sleep to name a few. With over 20 successful years conducting phase I-IV trials and headq...
Mattson Resources, LLC Orange County, CA, CA
Clinical Research Associate ESSENTIAL DUTIES AND RESPONSIBILITIES include the following. Other duties may be assigned. • Organize and manage Clinical Studies, assist in developing Clinical Protocols and Data Analysis. • Provide oversight ensuring protocol compliance and close monitoring of study subjects. Responsible for all data and source documentation, adverse experience reporting and mainte...
St. Jude Medical, Inc. Plymouth, MN
Description We are seeking an experienced, high caliber Senior Clinical Research Associate. Working independently with minimal guidance and direction, assists in the planning and conduct of SJM clinical studies. Ensure compliance to study protocol, domestic and international Good Clinical Practices, applicable regulatory standards, and SJM Standard Operating Procedures. Able to solve complex prob...

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!

Popular Articles

Transportation and Warehousing Jobs Article Rating
Transportation and warehousing workers move materials around the country. Learn about jobs in this sector.
Engineering Jobs Article Rating
Engineers of all specialties are in demand. Explore careers in the engineering industry and search for engineering jobs now.
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: 2015.5.0.7-323
eTrustLogo