Job Description Summary

The candidate will provide a full range of technical and professional research services in the Addiction Sciences Division of MUSC for Dr. Erin McClure. The candidate will be located at MUSC Charleston and will be responsible for oversight of Dr. McClure’s ongoing trials. The candidate will work closely with MUSC Charleston research staff and remote research staff in Pickens, SC. Job responsibilities include handling administrative responsibilities for studies, reporting on outcomes and progress, training research staff and complying with Good Clinical Practice standards, and working in collaboration with the remote Program Manager at Pickens to ensure successful execution of all ongoing studies. Specific tasks may include; overseeing subject recruitment, data collection and management, data quality control and data audits, purchasing study supplies and managing supply inventory, working with the Program Manager in assuring regulatory compliance, building and maintaining REDCap study databases. This role may include supervisory duties such as training and overseeing Program Assistants and signing off on timesheets and time off requests. The candidate will have exceptional organizational, management and interpersonal skills and be able to manage tasks across several ongoing studies. Experience with REDCap is highly preferred, as well as experience working on multi-site clinical trials. Finally, the candidate must have exceptional interpersonal skills and be able to work collaboratively with research staff, remote site staff, medical clinicians, administrative staff, and study subjects.

Entity

Medical University of South Carolina (MUSC - Univ)

Worker Type

Employee

Worker Sub-Type​

Research Grant

Cost Center

CC001039 COM PSYCH Addiction Science CC

Pay Rate Type

Hourly

Pay Grade

University-05

Pay Range

38,985.00 - 55,559.50 - 72,134.000

Scheduled Weekly Hours

40

Work Shift

Job Description

FLSA: Hourly

Work Schedule: Monday - Friday, 8:30AM - 5:00PM; This may position may involve occasional weekend (~1 per month) and weekday evening hours.

Remote Work: No remote option for work initially, but remote work options can be considered for 1 day per week after 6 months of employment.

Job Duties:

• 20% - Manages fiscal responsibilities including but not limited to, study invoices, purchasing card reconciliation, works and OurDay documentation, and participant remuneration. Stays up to date with fiscal trainings and proper procedures.
• 20% - Supervisory duties including training and supervision for Program Assistants and reviewing/monitoring overall performance. Signs off on time sheets as well as time off requests as Dr. McClure sees fit. Serves as expert resource for junior staff members and addresses questions and concerns, in addition to addressing performance issues and resolutions.
• 15% - Assists the Program Manager with preparing, developing, reporting, submitting and maintaining communications with the IRB, OCR, PRA, NIH, and clinicaltrials.gov regarding grant development (drafting protocols and consents for the PI), recruitment milestones, study design/procedures, adverse events and reporting, protocol deviations, study renewal, study termination, study amendments, and other activities necessary for regulatory compliance.
• 10% - Develop and update local standard operating procedures and study flow that is consistent with the protocol; Develop site and study specific recruitment procedures including all study advertising; monitor for effectiveness and revise as appropriate. Work closely with research staff and PI to ensure all aspects of the study are in accordance with the Code of Federal Regulations, Good Clinical Practice, and MUSC Policies.
• 10% - Detects issues related to data capture, collection or management and suggests solutions. Respond promptly to resolving any data query issues such as inconsistent data collection from participants, incorrect reports, malfunctions in databases or other technology for data collection utilized in multiple studies. Coordinate and manage tracking of all research participants including but not limited to, recruitment and advertisement tracking and retention rates.
• 10% - Provide oversite and management of protocol supply inventory including study mailing materials, study devices, and handles all shipping for participant supplies.
• 10% - Ensure recruitment and timeline goals for studies are met. Under minimal to no supervision, develops and implements strategies to increase research participation, retention, and follow up rates, such as advertisements across new social media platforms, participant reminders via email/text, and consulting with other MUSC research teams/recruitment companies. Takes a proactive approach to addressing issues and barriers to study enrollment, recruitment and follow-up.
• 5% - Works collaboratively with research staff from multiple study sites to ensure consistency in procedures, addressing issues and maintaining data integrity and high data quality and appropriate progress on studies.

MUSC Minimum Training and Experience Requirements: A bachelor’s degree and two years of relevant program experience.

Preferred Training and Experience: A bachelor’s degree and 2 years of relevant program experience, with at least one full-time clinical research position. A background in human subjects research is required. Ability to collect, organize, and analyze information in a clear and concise manner. Ability to think critically, proactively address potential issues and solutions, and effectively manage time and tasks through exceptional organizational skills. Ability to establish and maintain effective working relationships with physicians, sponsors, other health care professionals, other research teams, administrative staff, etc. A background in research, including in the development of electronic research databases within REDCap is strongly preferred. Previous experience with managing staff or serving in a supervisory role is preferred.

Additional Job Description

Minimum Requirements: A bachelor’s degree and two years of relevant program experience. Physical Requirements: (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.

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