Translational Research Coordinator I - San Diego, United States - UC San Diego Health

UC San Diego Health

Verified Company

San Diego, United States

3 weeks ago

Posted by:

Mark Lane

beBee recruiter

Description

Payroll Title:

CLIN RSCH CRD AST
Department:
CANCER CENTER/ Clinical Trials Office
Hiring Pay Scale

- $ $49.94 / Hour

Worksite:
Moores Cancer Center
Appointment Type:
Career
Appointment Percent:
100%
Union:
RX Contract
Total Openings:
2
Work Schedule:
Days, 8 hrs/day, Monday
Friday
#128211 Translational Research Coordinator I:

Extended Deadline:
Mon 4/29/2024**
UC San Diego values equity, diversity, and inclusion.
If you are interested in being part of our team, possess the needed licensure and certifications, and feel that you have most of the qualifications and/or transferable skills for a job opening, we strongly encourage you to apply.

DESCRIPTION:

The Clinical Trials Office (CTO) at UCSD's Moores Cancer Center administers many clinical trials on behalf of its member investigators, including trials sponsored by National Cancer Institute cooperative groups, pharmaceutical companies, and physician investigators.

Reporting directly to the Translational Project and Lab Manager, the Translational Research Coordinator I supports the clinical research efforts of the MCC by providing comprehensive coordination and data management for a portfolio of translational research protocols.

The incumbent is responsible for supporting and coordinating translational research protocols, including recruitment, consenting, research chart preparation, data collection and record-keeping, and ensuring all protocol requirements are met.

Assure compliance with state and federal regulatory guidelines. Assist in ensuring the quality of the medical and clinical research data. Assist in providing guidance to investigators. Provide education and information to the general public concerning the ongoing clinical trials. Assist PIs with proposals, progress reports and manuscripts. Under direct supervision, create original documents and policies for assigned disease teams. Work closely with federal and state regulatory officials.

MINIMUM QUALIFICATIONS:

Theoretical knowledge and/or Bachelor's Degree in social science, biological sciences, or a related field, and/or an equivalent combination of education and experience.
Demonstrated advanced organizational and project management skills (preferably in an academic setting), including the ability to work independently, determine priorities, complete multiple projects accurately, efficiently, and with a high level of attention to detail while working with conflicting deadlines.
Experience performing clinical research duties in a clinical research environment such as CRO, academic research institution, and/or a research hospital.
Experience handling, transporting, and/or processing biospecimens such as blood, tissue, and urine.
Experience in research protocol startup procedures, including: study feasibility, study activation and IRB processes, and qualification procedures. Experience in clinical trials research including budget negotiations and invoicing per clinical trial agreement.
Excellent written skills and knowledge of the English language, including grammar, spelling, and punctuation usage. Ability to compose, edit, and finalize correspondence.
Interpersonal skills with strong, demonstrated ability to communicate orally and in writing. Possess skills of tact, poise, diplomacy, confidentiality, and flexibility. Ability and willingness to work independently and/or in a team framework in conjunction with principles of community and with a diverse population of staff, faculty, and members of the community.
Ability to demonstrate a high degree of professionalism in a rapidly changing, timepressured environment. Independent judgment, strong organizational skills, and the ability to be flexible as demands and priorities change.
Working knowledge of investigational protocols (data management, query resolution, protocol design and protocol implementation). Working knowledge of medical and scientific terminology.
Knowledge of experimental protocols, data gathering, protocol design and evaluation.
Ability to maintain confidentiality.
Experience in clinical trials research.
Demonstrated experience in research protocol procedures, design, monitoring, Human Subject Rights, and informed consent procedures.
Experience with laboratory procedures and values and experience interpreting them to determine patient eligibility and potential toxicities.

PREFERRED QUALIFICATIONS:

Bachelor's degree in related area and / or equivalent experience / training.
Certification as a Clinical Research Associate or Coordinator.
Experience completing clinical trials case report forms via hard copy and online.
Enthusiasm for learning and a genuine interest in scientific research. Willingness and ability to learn new skills, research methods, and scientific principles.
Theoretical knowledge of oncology clinical research trials.

SPECIAL CONDITIONS: