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Field Clinical Research Associate Jobs

Research Field Technician Jobs
By University of Arkansas At , Stuttgart

Please do not send to listed recruitment contact.

All application information is subject to public disclosure under the Arkansas Freedom of Information Act.

Clinical Research Associate Ii - Phoenix / Tucson
By ICON At , Phoenix
Knowledge of ICH and local regulatory authority regulations regarding drug
Experience in monitoring all trial components (PSSV to COV)
Ability to travel as needed (greater than 40%)
Clinical Research Associate (Cra)
By Peachtree BioResearch Solutions At Atlanta, GA, United States
Work closely with the Site Management team and sponsor stakeholders so you can plan and manage your work most effectively
Work with Peachtree's Data Management team and sites to ensure all queries are resolved
1-5 years of experience working on clinical trials (CRO or Sponsor) as either a coordinator or CRA I
Experience with CNS, rare disease and/or oncology studies preferred
Experience working in a CTMS and EDC system
Excellent organizational and critical thinking skills
Clinical Research Associate Jobs
By Candel Therapeutics At Needham, MA, United States
Knowledge of project management tools and practices, and proficiency in using normal office software; Microsoft Word, Excel and PowerPoint.
Participate in maintaining accuracy within clinical management systems and internal reports and trackers.
Able to manage multiple projects independently and use varying databases and management systems.
Minimum 1-3 years relevant clinical research experience.
Excellent verbal and written communication skills, good organizational and interpersonal skills, and a team drive.
Knowledge of GCP and FDA regulations related to clinical trial conduct and familiarity with industry best practices.
Associate Clinical Research Associate (Remote -West Region)
By Merck Sharp & Dohme At , Rahway, 07065, Nj $72,880 - $114,600 a year
Developing skills in Site Management including management of site performance and patient recruitment
Effective time management, organizational and interpersonal skills, conflict management
Able to work with other experienced research professions to develop skills across multiple protocols, sites and therapy areas.
Coordinates & manages various tasks in collaboration with other sponsor roles to achieve Site Ready.
Manages and maintains information and documentation in CTMS, eTMF and various other systems as appropriate and per timelines.
Good understanding and working knowledge of clinical research, phases of clinical trials, current GCP/ICH & country clinical research law & guidelines.
Clinical Research Associate, Sponsor Dedicated
By IQVIA At , Remote
Alternatively, you should have an equivalent combination of education, training and experience
A Bachelor's degree in a health care or other scientific discipline or educational equivalent
2 years of clinical research coordinator experience strongly preferred
While projects vary, your typical responsibilities might include:
We are committed to providing equal employment opportunities for all, including veterans and candidates with disabilities. https://jobs.iqvia.com/eoe
Performing site selection, initiation, monitoring and close-out visits, plus maintaining appropriate documentation
Clinical Research Associate Jobs
By Lyra Therapeutics At Watertown, MA, United States

Lyra Therapeutics, Inc. is a clinical-stage biotechnology company developing novel, integrated drug and delivery solutions for the localized treatment of patients with chronic rhinosinusitis (CRS) ...

Clinical Research Associate (Cra) - B
By Intellectt Inc At Alameda, CA, United States
5+ years of relevant experience in site monitoring and clinical project management.
Project management and organizational skills.
Communicate study progress to management.
Understanding of clinical trial process, data management, and analysis.
Manage clinical monitoring, site compliance, and adherence to protocols.
Experience in medical device, in-vitro diagnostics, or pharmaceutical studies.
Clinical Research Associate (Cra)
By LumaBridge At United States
Ability to independently prioritize tasks with excellent time management skills.
Create and maintain appropriate documentation regarding site management, monitoring visit findings and action plans.
Perform other duties as assigned by management.
Excellent verbal and written communication skills and conflict resolution abilities.
Oversee and conduct monitoring activities, including remote monitoring and risk-based monitoring.
Lead assigned sites through regular contact to ensure site compliance, adequate enrollment, and understanding of study requirements.
Clinical Research Associate Jobs
By WEP Clinical At Raleigh-Durham-Chapel Hill Area, United States
High organizational and logistics skills to ensure effective management of multiple sites and protocols within timeframes and on budget
Approximately 2-5 years of on-site and remote monitoring experience
Broad range of therapeutic experience
Superior written and verbal communication skills
Wren Nursing (Clinical Trial Home Nursing & Clinical Education)
Contribute to the development of protocols, study tools, materials, and documentation for clinical sites.
Clinical Research Associate Jobs
By ProTrials Research, Inc. At , $85,000 - $120,000 a year
Bachelor and/or advanced degree in biological sciences or related field, or equivalent combination of relevant experience, education or training
Managing and training of site personnel on therapeutic area, protocol requirements, proper source documentation, and case report form completion
Excellent organizational skills, strong interpersonal and communications skills, and strong problem-solving skills
Extensive knowledge of FDA regulations and their practical implementation
2 years of prior experience as a Clinical Research Associate preferred
Full medical, dental, and vision benefit packages
Clinical Research Associate-208919 Jobs
By Medix™ At Florida, United States

The CRA is expected to work cooperatively with study team and operations management to proactively drive project success.

Research Field Technician Jobs
By Colorado State University At Fort Collins, CO, United States
Pursuing a degree in Natural Resources Management, Soil and Crop Sciences, or closely related fields.
Willingness to learn to work with basic vendor-supplied programs and other data management software unique to field equipment.
Ability to communicate (public speaking and writing skills)
Previous experience in research farms
Experience with data recording, handling, and analysis
Expertise with basic spreadsheet data (i.e., MS Excel)
Cra (Clinical Research Associate)
By Agilent Technologies At Washington, DC, United States
Assist with site audits and site quality management activities, as needed.
Ensure monitoring activities (remote and on-site) are completed in accordance with Agilent procedures and study monitoring plan.
Assures adherence to GCP, study protocol, and all applicable requirements through routine monitoring visits.
2+ years direct clinical research experience at a sponsor or CRO as a CRA/study monitor, or equivalent experience.
Diagnostic/IVD experience highly preferred, oncology or other medical device experience is also accepted.
Previous experience with NGS, IHC, or pathology highly preferred.
Clinical Research Associate Jobs
By ProKatchers LLC At West Sacramento, CA, United States
Position Requirements: Bachelor's degree in a Life Science or related field with 2+ years’ experience in laboratory experience.
Location:West Sacramento CA 95691 United States
Pay Rate:$45/ HR to $50/ HR
Clinical Research Associate Jobs
By Pharmaron At Washington DC-Baltimore Area, United States
Escalate any site issue to the Clinical Trial Manager and/or study team, as needed.
Develop in-depth knowledge in relevant indications and clinical study methodology.
BA degree or RN or higher, preferentially in sciences/medical sciences, or equivalent experience.
At least 5 years of clinical monitoring experience.
At least 8 years of experience in the pharmaceutical industry or clinical research site-based experience.
Knowledge of ICH GCP guidelines.
Clinical Research Associate Jobs
By Sarah Cannon At Nashville, TN, United States
Prior significant clinical/scientific background and/or education is required.
Serve as the primary point of contact for investigational sites.
Conduct investigational product accountability to ensure accuracy, proper storage, dispensation and reconciliation.
It’s More Than a Career, It’s a Mission.
About Sarah Cannon Research Institute
Clinical Research Associate Jobs
By Mindlance At Maple Grove, MN, United States
Look for candidate who has some documentation and some clinical research experience and computer savvy
System used is called CDO Gateway for the regulatory docs - medical documents experience is NOT required
Will consider someone with No College Degree as long as they have the necessary experience
Duration:04-05 months Contract, may extend further depends on the business need of project and performance.
will be reviewing regulatory documents, uploading, filing them and moving to their program.
Must be self-motivated, analytical, organized, and exercise accuracy
Field Clinical Specialist Jobs
By Abiomed At Virginia, United States
Typically a minimum of 5 years of relevant clinical experience, with in-depth knowledge of cardiology, and related cardiovascular technologies
Develop and maintain knowledge of clinical sites in the assigned territory.
Understand and assess investigators’ interests and qualifications.
Identify appropriate investigators as defined by study-specific requirements and by the applicable regulatory code.
Manage the following aspects of study progress, including, but not limited to:
Nominate, approach, and complete qualification processes including establishing site/sponsor expectations for study execution.
Clinical Research Associate Jobs
By KlinEra Global Services At San Francisco Bay Area, United States
Excellent interpersonal, judgment, and time management
You will also manage regular site liaison, tracking, query resolution, and maintaining investigator site file and TMF.
Approximately 3-5yr Experience as Clinical Research Associate
Fundamental knowledge and good understanding of GCP’s, clinical study development process, and logistics.
Proficient knowledge of MS Office Applications (Word, Excel, PowerPoint, Etc.
Support study start-up activities including site selection, collecting essential documents and CTRA, register study on ANZCTR.