Clinical Research Associate 1
allen spoldenDenver, CO
Clinical Research Associate 1
L4
allen spoldenDenver, CO32 days ago
Occupations
Clinical Research CoordinatorsHealthcare Support Workers, All OtherClinical Data ManagersIndustries
Research and Development in the Physical, Engineering, and Life SciencesResearch and Development in BiotechnologyOther Scientific and Technical Consulting ServicesJob Title Responsible for providing Clinical Research support for all clinical trials.
Job Description:
Under the direction of supervisor or designee, this position will serve as support for the clinical study team.
Essential Duties And Responsibilities:
Participate and assist in design and preparation of protocols and case report forms. Generate clinical SOPs, policies, charters, and plans according to US and international guidelines. Participate in the evaluation of potential clinical sites according to established criteria of acceptability. Responsible for procurement of budgets, contracts, regulatory documents, and other administrative documents as related to clinical research functions. Initiate studies performing initiation site visits, arrange for shipment of clinical supplies, case report forms, and other necessary materials. Conduct ongoing study monitoring, including frequent periodic site visits, protocol adherence checks, material handling procedures, inspection of study files, and related monitoring functions. Prepare site visit reports with identification of key accomplishments, key issues for resolution and recommendations for follow-up actions for assigned study sites. Conduct study termination visits, obtain final reports from investigators, and participate in the preparation of final reports for regulatory submission. Assist with the maintenance of clinical archive and electronic files. Other tasks as assigned.
Requirements:
To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. BA, BS, RN, BSN or equivalent Basic knowledge and adherence to GCPs 1-2 years of clinical research experience or equivalent experience or training Strong attention to detail Ability to multi-task Unquestionable integrity and highest ethical standards Excellent written and verbal communication skills Self-motivated, assertive, and driven Benefits Dental, Medical, Vision, PTO and 401K
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Level
MidL4
Location
Denver, CO
Occupation
Clinical Research Coordinators
Industry
Research and Development in the Physical, Engineering, and Life Sciences
Posted
32 days ago
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