UNIV - Pediatrics Precision Medicine Coordinator - Hollings Cancer Center

Summary The Clinical Trials Office is recruiting a Pediatric Precision Medicine Coordinator to work with the Pediatrics' team. Under general supervision of Clinical Trials Office leadership and in collaboration with clinical operations, data core, laboratory, quality, information technology, pathology, and physician partners, this position coordinates and supports complex oncology clinical research programs at the Medical University of South Carolina, Hollings Cancer Center, and Shawn Jenkins Children’s Hospital.

The position integrates protocol and data management, study participant coordination, biospecimen operations, and quality oversight in cooperation with the Children’s Oncology Group, research consortium, investigator-initiated, industry-sponsored, translational, and precision oncology initiatives. Independent professional judgment is required to ensure data integrity, protocol compliance, operational efficiency, and timely communication with investigators, sponsors, research bases, and institutional partners.

This position will be located on the Charleston campus and will split their time between Hollings Cancer Center and Shawn Jenkins Children’s Hospital. Entity Medical University of South Carolina (MUSC - Univ) Worker Type Employee Worker Sub-Type​ Research Grant Cost Center CC001332 HCC CTO Administration Pay Rate Type Salary Pay Grade University-GEN09

53,142.00 - 71,706.00 - 90,372.000 Scheduled Weekly Hours 40 Work Shift

The Clinical Trials Office is recruiting a Pediatric Precision Medicine Coordinator to work with the Pediatrics' team. Under general supervision of Clinical Trials Office leadership and in collaboration with clinical operations, data core, laboratory, quality, information technology, pathology, and physician partners, this position coordinates and supports complex oncology clinical research programs at the Medical University of South Carolina, Hollings Cancer Center, and Shawn Jenkins Children’s Hospital.

The position integrates protocol and data management, study participant coordination, biospecimen operations, and quality oversight in cooperation with the Children’s Oncology Group, research consortium, investigator-initiated, industry-sponsored, translational, and precision oncology initiatives. Independent professional judgment is required to ensure data integrity, protocol compliance, operational efficiency, and timely communication with investigators, sponsors, research bases, and institutional partners.

This position will be located on the Charleston campus and will split their time between Hollings Cancer Center and Shawn Jenkins Children’s Hospital.

35% - Clinical Research Data Management and Quality Submit complete, accurate, and timely data to the Children’s Oncology Group, research consortiums, industry sponsors, institutional databases, and other research systems for assigned studies and participant caseloads. Maintain research records, source documentation, case report forms, screening logs, adverse events and concomitant medication logs, protocol deviations, patient-reported outcomes, radiology records, staging documentation, and other protocol-required materials.

Perform chart abstraction and source verification; resolve sponsor, monitor, database, imaging, and research-base queries within required protocol timelines. Support secondary data reviews for baseline and follow-up time points to resolve quality or performance concerns. Support monitoring visits, audits, inspections, corrective and preventive actions, and performance metric review.

Protect participant privacy and the confidentiality of clinical and molecular data. 30% - Clinical Research Coordination and Participant Management Coordinate study activities for the Pediatric Hematology/Oncology Investigators, including informed consent support, enrollment, follow-up, and off-study requirements. Interpret protocols, informed consent documents, study calendars, laboratory manuals, and sponsor guidance to plan and coordinate protocol-required procedures and assessments.

Collaborate with investigators, nurses, pharmacy, pathology, radiology, laboratory personnel, ancillary departments, and study participants to ensure required activities occur within protocol-defined timeframes. Maintain accurate participant status in the clinical trial management system and electronic medical record (EMR), including timely encounter updates for screening, enrollment, follow-up, and study completion.

Participate in Clinical Research Group (CRG) clinics, meetings, and tumor boards to identify potential participants and support continuity of clinical research operations. 20% - Biospecimen, Laboratory, and Protocol Support Coordinate the collection, preparation, processing, transport, shipment, tracking, and submission of blood, pathology, molecular, pharmacokinetic, pharmacodynamic, and other biologic specimens according to protocol and laboratory manual requirements.

Handle biologic specimens and bloodborne pathogens in accordance with OSHA, IATA, institutional safety requirements, and departmental standard operating procedures. Manage laboratory kits and supplies using designated inventory and sample management systems. Coordinate radiology image, EKG, pathology, genomic, and other specialized submissions; maintain required portal access and resolve vendor or sponsor queries with internal departments. 10% - Precision Oncology Program Development Support cross-functional projects involving clinical trial systems, molecular data platforms, and sample management tools.

Coordinate day-to-day program activities and execute approved project plans, timelines, deliverables, and stakeholder communications. Cultivate effective partnerships with information technology, pathology and laboratory medicine, external molecular laboratories, sponsors, vendors, and other academic collaborators. 5% - Team Support and Other Responsibilities Promote a respectful, collaborative, service-focused work environment and respond to study team, sponsor, monitor, and participant inquiries in a timely and professional manner.

Maintain required training, competencies, credentials, and system access. Participate in staff meetings, huddles, continuing education, audits, monitoring visits, and departmental improvement activities. Perform other related duties and special projects as assigned to support the mission and operational needs of the Clinical Trials Office and Hollings Cancer Center.

Additional

Minimum

A bachelor's degree and two years of relevant program experience. Physical

(Note: The following descriptions are applicable to this section: Continuous - 6-8 hours per shift; Frequent - 2-6 hours per shift; Infrequent - 0-2 hours per shift) Ability to perform job functions in an upright position. (Frequent) Ability to perform job functions in a seated position. (Frequent) Ability to perform job functions while walking/mobile.

(Frequent) Ability to work indoors. (Continuous) Ability to work outdoors in all weather and temperature extremes. (Infrequent) Ability to work in confined/cramped spaces.

(Infrequent) Ability to perform job functions from kneeling positions. (Infrequent) Ability to squat and perform job functions. (Infrequent) Ability to perform 'pinching' operations.

(Infrequent) Ability to fully use both hands/arms. (Frequent) Ability to perform repetitive motions with hands/wrists/elbows and shoulders. (Frequent) Ability to reach in all directions.

(Frequent) Possess good finger dexterity. (Continuous) Ability to maintain tactile sensory functions. (Continuous) Ability to lift and carry 15 lbs., unassisted.

(Infrequent) Ability to lower objects, up to 15 lbs., from height of 36 inches to floor level, unassisted. (Infrequent) Ability to push/pull objects, up to 15 lbs., unassisted. (Infrequent) Ability to maintain 20/40 vision, corrected, in one eye or with both eyes.

(Continuous) Ability to see and recognize objects close at hand. (Frequent) Ability to see and recognize objects at a distance. (Frequent) Ability to determine distance/relationship between objects; depth perception.

(Frequent) Good peripheral vision capabilities. (Continuous) Ability to maintain hearing acuity, with correction. (Continuous) Ability to perform gross motor functions with frequent fine motor movements.

(Frequent) If you like working with energetic enthusiastic individuals, you will enjoy your career with us! The Medical University of South Carolina is an Equal Opportunity Employer. MUSC does not discriminate on the basis of race, color, religion or belief, age, sex, national origin, gender identity, sexual orientation, disability, protected veteran status, family or parental status, or any other status protected by state laws and/or federal regulations.

All qualified applicants are encouraged to apply and will receive consideration for employment based upon applicable qualifications, merit and business need. Medical University of South Carolina participates in the federal E-Verify program to confirm the identity and employment authorization of all newly hired employees. For further information about the E-Verify program, please click here: http://www.uscis.gov/e-verify/employees