Clinical Research Associate jobs in North Carolina
Recently Added Clinical Research Associate jobs
Senior Clinical Research Associate
- Catalyst Clinical Research
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Raleigh, NC
FULL_TIME
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Are you an experienced oncology CRA with experience in supporting colorectal, pancreatic or advanced solid tumor? We have a role for you!
Job Duties:
As a Senior Clinical Research Associate, you will monitor clinical trial programs and manage regional clinical trial sites to support biological and pharmaceutical developmental programs in a manner consistent with relevant regulations including ICH/GCP and PhRMA guidelines along with Catalyst Clinical Research’s applicable SOPs and working practices. You will collaborate with an assigned clinical research team to provide input on site selection, study initiation procedures, conflict resolution, and audit responses. You will effectively communicate all relevant and important findings with appropriate in-house personnel.
Specific responsibilities will include but are not limited to:- Travels up to 80% within an assigned territory, monitors clinical trials according to monitoring plans to achieve project goals; conducts or assists with site evaluations, study initiations, routine monitoring, site close-outs, and FDA audit preparations. Develops territory to broaden selection of research study sites
- Effectively communicates with site study staff and Catalyst clinical research personnel to report study site status, disseminate information to the appropriate individuals, and resolve study related issues; replies to audit findings
- Partners with assigned clinical project team.
- Assists with Investigator Meetings planning/presentations, data collection, and FDA submission preparations
- Maintains a home office if working remotely.
- Manages work activities in a time and cost-effective manner to ensure budgetary guidelines and project timelines are met
- Participates in internal and/or external meetings to maintain current knowledge on applicable regulations and guidelines.
- Collaborates closely with the Study Manager and Project Manager.
- Internal support is provided to the Field Monitor from the assigned Clinical Trial Associate
- Works closely with the extended study team including the Sponsor, Vendors, Data Manager(s), Statistician, Medical Monitor and other trial staff
- Bachelor’s degree in a science or health-related discipline or equivalent of 7 years industry experience
- Minimum of 5 years’ experience in clinical research with direct site monitoring experience with a sponsor company or CRO and 3 years of recent oncology clinical trial experience
- Strong knowledge of clinical trial monitoring, regulatory compliance, clinical research methodology and all applicable regulations and guidelines
- Strong organizational and time management skills and the ability to work independently
- Excellent communication and interpersonal skills
- Flexibility and ability to travel routinely to meet project requirements
- Strong knowledge of standard computer applications
Catalyst Clinical Research, LLC is an equal opportunity employer. We celebrate diversity and are committed to creating an inclusive environment for all employees.
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ZaIG268Ay8 - 7 Days Ago
Development associate
- Duke Clinical Research Institute
-
Durham, NC
FULL_TIME
- School of Medicine Established in 1930, Duke University School of Medicine is the youngest of the nation's top medical schools. Ranked sixth among medical schools in the nation, the School takes pride...
- Just Posted
BUSINESS DEVELOPMENT ASSOCIATE I, DCRI
- Duke Clinical Research Institute
-
Durham, NC
FULL_TIME
- School of Medicine Established in 1930, Duke University School of Medicine is the youngest of the nation's top medical schools. Ranked sixth among medical schools in the nation, the School takes pride...
- 1 Month Ago
Senior Clinical Research Associate - CNS - Mid-Atlantic
- Worldwide Clinical Trials - USA
-
Washington, NC
FULL_TIME
- Who we are Worldwide Clinical Trials (Worldwide), a leading global contract research organization (CRO), works in partnership with biotechnology and pharmaceutical companies to create customized solut...
- 9 Days Ago
Senior Clinical Research Associate - CNS - East Coast
- Worldwide Clinical Trials - USA
-
Washington, NC
FULL_TIME
- Who we are Worldwide Clinical Trials (Worldwide), a leading global contract research organization (CRO), works in partnership with biotechnology and pharmaceutical companies to create customized solut...
- 10 Days Ago
Chief Research & Technology Officer, DCRI
- Duke Clinical Research Institute
-
Durham, NC
FULL_TIME
- School of Medicine Established in 1930, Duke University School of Medicine is the youngest of the nation's top medical schools. Ranked sixth among medical schools in the nation, the School takes pride...
- 24 Days Ago
Clinical Research Associate jobs at Popular Companies
Clinical Research Associate
- McInnis Inc.
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Clinical Research Associate
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Clinical Research Associate
- Diverse Lynx
-
Philadelphia, PA
- Position Clinical Research Associate Location Philadelphia PA (Onsite) Job type:- Fulltime Job Description Qualification...
- 6/9/2024 12:00:00 AM
About North Carolina
North Carolina (/ˌkærəˈlaɪnə/ (listen)) is a state in the southeastern region of the United States. It borders South Carolina and Georgia to the south, Tennessee to the west, Virginia to the north, and the Atlantic Ocean to the east. North Carolina is the 28th-most extensive and the 9th-most populous of the U.S. states. The state is divided into 100 counties. The capital is Raleigh, which along with Durham and Chapel Hill is home to the largest research park in the United States (Research Triangle Park). The most populous municipality is Charlotte, which is the second-largest banking center in...
Source: Wikipedia (as of 04/11/2019). Read more from Wikipedia
Income Estimation for Clinical Research Associate jobs
$65,922 to $87,072
Most Popular Cities in North Carolina for Clinical Research Associate Jobs
What does a Clinical Research Associate do?
Clinical Research Associate in Vista, CA
Represents Global Clinical Affairs on multifunctional teams tasked with preparing responses to regulatory agencies.
May 02, 2023
Clinical Research Associate in Stockton, CA
Document informed consent discussion and obtain signatures per protocol, federal, state and institutional requirements.
April 20, 2023
Clinical Research Associate in Stamford, CT
Responds flexibly to changing business demands and opportunities, proactively looking for ways to contribute.
May 09, 2023
Participate in monitoring visit report review process in order to maintain oversight of clinical monitoring quality and adherence to protocol and established processes and plans.
December 03, 2022