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5 days old

Clinical Research Coordinator I (CRC I)

Kelly Services
Tulsa, OK 74152
**Clinical Research Coordinator, RN**







Kelly services is currently seeking a Clinical Research Coordinator, RN for one of our top clients in Healthcare in the Tulsa, Oklahoma area. The Clinical Research Coordinator, under minimal supervision, is responsible for enlisting and maintaining patients on research protocol regimens.







**Responsibilities:**






+ Assists with delegated patient education regarding general open trial information available at OCSRI.

+ Presents trial concepts and details to the patients and participates in the informed consent process under the direction of the physician.

+ Participates in ongoing patient education: study drug and standard of care mechanism of action, study drug and standard of care treatment side effects, symptom management, disease status, community resources, and specific protocol requirements.

+ Maintains Research Clinical Trial Participant Management according to specialists and Research Institute Research Standard Operating Procedure (SOP). (RES500 RES515)

+ Maintains research patient database to maintain compliance of our NCI parent institution requirements.

+ Assesses patient for changes in condition, adverse events, concomitant medication use, protocol compliance, response to study drug. Works closely with physician and clinic staff to ensure protocol compliance.

+ Flags patient medical record with protocol-specific communication and documentation to alert all staff regarding protocol requirements for each patient on a clinical trial. Acts as a resource for clinical staff by reporting protocol activities at staff meetings as needed.

+ Works directly with the physician/investigator to assure understanding of study requirements, dose modification requirements, adverse event reporting, and documentation needs.

+ Participates in and supports all site auditing and monitoring visits as well as all Pre-Study Site Visits/Site Initiation Visits as required.

+ Maintains training as required by the sponsors and NCI protocol guidelines (i.e. eCRF, ePRO, IVRS/IWRS, EKG, Lab/Tissue databases, etc).

+ Coordinates with the Regulatory Coordinators as needed to ensure all regulatory requirements are maintained for all research patients in screening, active treatment, and follow-up.

+ Reviews initial protocol and all protocol amendments provided by the regulatory coordinator and/or manager. Reconsents and educates patients on interim protocol findings/changes as needed per IRB guidance.

+ Assess and reports all Serious Adverse Events as required per protocol and IRB guidelines.

+ Develops audit responses and corrective action plans in coordination with the lead study coordinator.

+ Actively participates in protocol initiations and study specific educational programs. Communicates and collaborates on an ongoing basis with sponsors and their representatives.

+ Acts as a liaison between the PIs/treating investigators and the sponsor or NCI medical monitors and study chairs to ensure protocol requirements are maintained, treatment-related dose modifications are carried out accurately, side effects are managed appropriately, and other communication as needed.

+ Coordinates with the Admixture staff to ensure adequate drug inventory is available for research patient care. Provides additional information for the admixture staff as needed for mixing, handling, and storage of investigational drug. Assists with drug accountability for research-related drug inventory.

+ Stores, dispenses, and maintains accountability for all oral investigational drugs in accordance with protocol requirements and USP 800 guidelines.





**Qualifications:**




+ Graduate from an accredited program for nursing education (BSN preferred)

+ Minimum seven years experience, preferably in oncology

+ Experience in medical research preferred

+ Current licensure as a registered nurse in state of practice

+ Current BLCS or ACLS certification required

+ ACRP or CCRC certification or OCN certification preferred

+ Knowledge of OCSRI policies and procedures

+ Knowledge of current FDA regulations, and Good Clinical Practices, governing clinical research,




**Why Kelly** **** **?**



Kelly Science & Clinical is your connection to premier scientific and clinical companies looking to hire talented people just like you. Every day, we match science professionals with dream jobs that fit their skills and interestsits the way we think job searching should be. Nearly 100 percent of our science recruiters have a professional background/education in science, so we know a thing or two about the science market and how to get you noticed.




**About Kelly** ****



At Kelly, were always thinking about whats next and advising job seekers on new ways of working to reach their full potential. In fact, were a leading advocate for temporary/non-traditional workstyles, because we believe they allow flexibility and tremendous growth opportunities that enable a better way to work and live. Connecting great people with great companies is what we do best, and our employment opportunities span a wide variety of workstyles, skill levels, and industries around the world.


Kelly is an equal opportunity employer committed to employing a diverse workforce and providing accommodations for people with disabilities in all parts of the hiring process as required under its Employment Accommodation Policy. Kelly will work with applicants to meet accommodation needs that are made known to Kelly in advance.

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Posted: 2020-09-14 Expires: 2020-10-15

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Clinical Research Coordinator I (CRC I)

Kelly Services
Tulsa, OK 74152

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