Clinical Translational Research Coordinator I – Hematology/Oncology

Vanderbilt University Medical Center•Nashville, TN

2d•Onsite

About The Position

With guidance and training, is responsible for coordinating the approval processes and conduct of oncology clinical research protocols/studies in the Holowatyj Laboratory & Team, such that the integrity and quality of the clinical/translational research is maintained, the study objectives are accomplished, and the research is conducted in accordance with Good Clinical Practice Guidelines, federal and sponsor regulations and guidelines, Vanderbilt Policy and Procedure and research protocols. Manages screening, implements recruitment procedures, consent, enrollment, randomization, and study conduct from planning through study closeout. Performs or implements processes to assure study-related procedures are performed as required and objectives and timelines are met. Maintains accurate and timely documentation and communication with Investigators, participants, IRB, sponsors, and other research-related entities.

Requirements

Bachelor's Degree (or equivalent experience) (Required)
< 1 year professional research experience (Required)
Exceptional organizational skills, attention to detail, and demonstrated human relations and effective communication skills (Required)

Nice To Haves

Phlebotomy experience (Preferred)
Prior experience in coordinating hematology/oncology studies (Preferred)

Responsibilities

Conveys a basic knowledge and understanding of policies, procedures, and regulations governing human subjects' research and incorporates them in the conduct of research.
Possesses a basic awareness of the Federal regulations and guidelines governing the protection of human subjects (e.g., FDA, OHRP, GCP/ICH guidelines, and HIPAA regulations), before engaging in human subjects research.
With assistance, prepares and processes new IRB research proposals, amendments, continuing review applications, and adverse event reports according to institutional and departmental policies and procedures and federal regulations.
Communicates a basic knowledge and understanding of the management and implementation of clinical/translational research operations.
Exhibits the capability to understand and follow a clinical/translational study protocol, obtaining training and seeking assistance when needed, to safely and accurately perform or assess required protocol procedures. Uses coordination skills and works collaboratively with study participants, other staff and departments to complete research protocols, including performing study procedures such as assessing participant eligibility and recruitment, arranging necessary schedules and procedures, completing required participant registration in StarPanel, conducting interviews and laboratory and diagnostic studies, tracking medication usage and other protocol specific investigational procedures.
Prepares and maintains documents required to be maintained and available internally and for regulatory authorities and/or the sponsor before, during, and after the conduct of a clinical/translational trial. Participates in periodic site visits from sponsor, regulatory authorities, and others to review research, source documentation, and research procedures.
Procures equipment and supplies needed to fulfill project requirements.
Participates in the determination of eligible candidates for study participation, assuring participants fulfill eligibility requirements.
Records data from source documentation and/or participant interaction onto case report forms (either paper or electronic) with awareness and attention to the requirements for accuracy, completeness, and timeliness. Attends to query resolution in a timely manner. Assures research information is collected and stored in a manner that is compliant with regulations/policies and good clinical practice.
Develops and maintains patient databases, investigational logs, and records of procedures followed
Familiar with the safety reporting requirements of the study protocol, FDA, and other regulatory bodies. In a timely fashion, monitors, detects, and reports adverse events, meeting the requirements of regulatory bodies. Coordinates activities and gathers information from a variety of sources to achieve stated outcomes.
Performs packaging and ships study specimens (blood, urine, etc.) to the sponsor or laboratory in accordance with sponsor and shipping guidelines and regulations, maintaining appropriate documentation.
With direction assists with study completion, study closeout and archiving of study files, ensuring completeness and continuity of all study data, performing ongoing checks of clinical/translational data that has been entered on the case report forms (paper or electronic) or in reports.
With supervision, develops and manages study budgets, monitoring efficient invoicing and taking appropriate action to maintain clinical trial billing compliance.
Assists the Principal Investigator in the development of study protocols.
Collaboratively participates in study team meetings. Maintains open and positive communications with investigators, participants, co-workers, other departments and sponsors.
Coordinates with referring physicians to provide information regarding available research projects and to maintain a strong referral basis.
Serves as an advocate for human subjects by establishing and maintaining communication with Investigators, research staff, Sponsors, participants and representatives of professional organizations, participant advocates, and the public responsible for, or concerned about, protections for human participants of research and through ongoing monitoring of trial processes and participants.
With guidance, assesses and evaluates potential participants pertinent medical and historical information to ensure only appropriate subjects are enrolled in clinical/translational trials and remain eligible for continued participation. Engages in open and positive communication with study participants and coworkers.
Participates in the ongoing informed consent process, ensuring that human subjects, their families, and other health care providers clearly understand what is expected of and from them in the course of participating in a clinical/translational trial.
Monitors enrollment goals and initiates strategies to promote enrollment and participant compliance.
Encourages open communication with participants by providing them with contact information and being available to answer, address or refer their calls.
With direction, performs or instructs others in performing procedures for research as they are described in the protocol, deviating from the protocol only when a subject's safety is at risk and in a timely manner reports all deviations from the protocol to the Principal Investigator and/or senior personnel who will determine if a protocol amendment or other safety reporting to appropriate funding/regulatory agencies is required.
Utilizes or obtains knowledge of disease processes to observe for and report adverse events in a timely and accurate manner to the principal investigator and all regulatory authorities (IRB, Sponsor, FDA, NIH, etc.) as required by protocol, policies and procedures and regulations.
Actively identifies and participates in training, education, and development activities to improve own knowledge and performance to sustain and enhance professional development. Pursues avenues to continue education (i.e., in-services, seminars, etc.)
Demonstrates initiative for continuous learning, both self-directed and as evidenced by attendance of educational and professional development opportunities. Actively seeks new learning opportunities, seeing learning as part of work.
Engages in a minimum of 5 hours of continuous, job-related educational activities annually or pursuing an advanced career-related academic education or certification.
Participates in and maintains certifications, licensure and credentialing as required by Vanderbilt, the department and Sponsor.
Participates in research-related programs, such as the Clinical/Translational Research Staff Council, by reviewing information and attending meetings open to research staff.
Furthers knowledge base by attending a Basic Research 101 within the first three months of employment date.