Clinical Research Associate jobs in Georgia
Recently Added Clinical Research Associate jobs
Senior Clinical Research Associate
- Everest Clinical Research
-
Watkinsville, GA
FULL_TIME
-
Everest Clinical Research (“Everest”) is a full-service contract research organization (CRO) providing a broad range of expertise-based clinical research services to worldwide pharmaceutical, biotechnology, and medical device industries. We serve some of the best-known companies and work with many of the most advanced drugs, biologics, and medical devices in development today.
Everest has been an independent CRO since 2004 with a strong foundation as a statistical and data management center of excellence. Building on this foundation, Everest has successfully developed and established itself as a full-service CRO. Everest’s headquarters are located in Markham (Greater Toronto Area), Ontario, Canada with additional sites in Little Falls (Greater New York City Area), New Jersey, USA, and Shanghai (Pudong Zhangjiang New District), China.
Everest is known in the industry for its high quality deliverables, superior customer service, and flexibility in meeting clients’ needs. A dynamic organization with an entrepreneurial origin, Everest continues to experience exceptional growth and great success.
Quality is our backbone, customer-focus is our tradition, flexibility is our strength…that’s us…that’s Everest.
To drive continued success in this exciting clinical research field, we are seeking committed, skilled, and customer-focused individuals to join our winning team as Senior Clinical Research Associates for coverage on the East Coast (Eastern time zone). The incumbents may be required to travel to other locations across the USA to support monitoring activities as necessary.
Key Accountabilities:- Interact with personnel from study sponsors, investigational sites, vendors, and Everest functional groups to enable timely and high quality initiations and completions of clinical trials.
- Identify, evaluate and qualify investigators and investigational sites for participation in clinical trials.
- Compile documentation for qualification of clinical sites. Review that documentation to ensure that those clinical sites comply with ICH-GCP and relevant local regulations.
- Assist with preparation and submission of regulatory documents to responsible authorities and IRB/ECs.
- Establish, maintain, and archive files of essential documents from investigative sites and for inclusion in Trial Master Files. These files must be maintained in a fashion so that they are continuously available for audit and completion for archive.
- Contribute to the development of documents that facilitate or describe the management of the clinical trial. Examples of such documents include Monitoring Plans, Risk Management Plans, study guides or manuals, and information collection tools.
- Develop and review documentation of information provided to study subjects, including informed consent forms.
- Assist with the preparation and negotiation of contracts with vendors and investigational sites.
- Participate in and prepare presentations for clinical trial initiation meetings such as investigator meetings or site monitor/coordinator training sessions. Address questions/concerns relevant to Clinical Operations from the meeting participants. Train Clinical Research Associates and site personnel on study requirements and procedures.
- Perform on-site monitoring of clinical studies.
- Document monitoring activities through submission of monitoring reports to Clinical Operations management for review, and through correspondence and telephone contact with investigative sites.
- Responsible for site management. Communicate directly with sites to provide direction, to assess performance, and to propose interventions to enhance enrollment performance.
- Monitor and report progress/status of investigational sites.
- Assist with investigator payments.
- Provide timely and accurate reports of travel expenses.
- Assist in the preparation, planning, and presentation of bid defenses.
- Participate in the development and maintenance of, and adhere to departmental SOPs and guidelines.
- Prepare, maintain, and complete training on study-specific and (or) applicable sponsor SOPs.
- Support sites in their efforts to prepare for audits conducted either by sponsors or regulatory authorities.
- Plan and carry out professional development.
- Bachelor’s degree in a life science or related field of study.
- Five years field monitoring clinical trials.
- Thorough knowledge of GCPs.
- Thorough comprehension of medical terminology.
- Excellent command of verbal and written English.
- Ability to travel a maximum of 70% of working hours is required.
We thank all interested applicants, however, only those selected for an interview will be contacted.
Everest is committed to upholding the principles of dignity, independence, integration, and equal opportunity. We welcome and encourage applications from people with disabilities, and upon request we will provide accommodations for candidates participating in any part of our recruitment and selection process. - 13 Days Ago
Senior Clinical Research Associate
- OnPoint Clinical Staffing Services
-
Atlanta, GA
FULL_TIME
- Job DescriptionSenior CRAResponsibilities include:* All aspects of study site monitoring including routine monitoring and close-out of clinical sites, maintenance of study files, writing of clinical t...
- 2 Days Ago
Clinical Research Regulatory Specialist
- Alcanza Clinical Research
-
Decatur, GA
FULL_TIME
- Department: Quality, Regulatory & SourceEmployment Type: Full TimeLocation: Accel Research Sites - Decatur, GAReporting To: Melissa HodgesDescriptionAlcanza is a growing multi-site, multi-phase clinic...
- 8 Days Ago
Research Assistant
- Alcanza Clinical Research
-
Decatur, GA
FULL_TIME
- Department: OperationsEmployment Type: Full TimeLocation: Accel Research Sites - Decatur, GAReporting To: Adrienne HillDescriptionAlcanza is a growing multi-site, multi-phase clinical research company...
- 5 Days Ago
Clinical Research Regulatory Specialist (Remote with travel to Decatur, GA site as needed)
- Alcanza Clinical Research
-
Decatur, GA
FULL_TIME
- Clinical Research Regulatory Specialist (Remote with travel to Decatur, GA site as needed)Department: Quality, Regulatory & SourceEmployment Type: Full TimeLocation: Accel Research Sites - Decatur, GA...
- 2 Months Ago
PRN Research Assistant
- Alcanza Clinical Research
-
Decatur, GA
PART_TIME
- PRN Research AssistantDepartment: Operations Employment Type: Part TimeLocation: Accel Research Sites - Decatur, GAReporting To: Adrienne HillDescriptionAlcanza is a growing multi-site, multi-phase cl...
- 26 Days Ago
Clinical Research Associate jobs at Popular Companies
Clinical Research Associate
- Advarra
-
- About Advarra: Advarra makes clinical research safer, smarter, and faster. Our integrated solutions help safeguard trial...
- 6/11/2024 12:00:00 AM
Clinical Research Associate
- Advarra
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- About Advarra: Advarra makes clinical research safer, smarter, and faster. Our integrated solutions help safeguard trial...
- 6/11/2024 12:00:00 AM
Clinical Research Associate
- Advarra
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- About Advarra: Advarra makes clinical research safer, smarter, and faster. Our integrated solutions help safeguard trial...
- 6/11/2024 12:00:00 AM
Clinical Research Associate
- Advarra
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- About Advarra: Advarra makes clinical research safer, smarter, and faster. Our integrated solutions help safeguard trial...
- 6/11/2024 12:00:00 AM
Clinical Research Associate
- Advarra
-
- About Advarra: Advarra makes clinical research safer, smarter, and faster. Our integrated solutions help safeguard trial...
- 6/11/2024 12:00:00 AM
Clinical Research Associate
- Advarra
-
- About Advarra: Advarra makes clinical research safer, smarter, and faster. Our integrated solutions help safeguard trial...
- 6/11/2024 12:00:00 AM
Clinical Research Associate
- OHSU
-
Portland, OR
- Function/Duties of Position The Clinical Coordinator works directly under a directors for the Center for Embryonic Cell ...
- 6/10/2024 12:00:00 AM
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 Georgia
Georgia is a state in the Southeastern United States.Beginning from the Atlantic Ocean, the state's eastern border with South Carolina runs up the Savannah River, northwest to its origin at the confluence of the Tugaloo and Seneca Rivers. It then continues up the Tugaloo (originally Tugalo) and into the Chattooga River, its most significant tributary. These bounds were decided in the 1797 Treaty of Beaufort, and tested in the U.S. Supreme Court in the two Georgia v. South Carolina cases in 1923 and 1989.
The border then takes a sharp turn around the tip of Rabun County, at latitude 35°N, thou...
Source: Wikipedia (as of 04/17/2019). Read more from Wikipedia
Income Estimation for Clinical Research Associate jobs
$66,402 to $87,707
Most Popular Cities in Georgia 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