Research Coordinator-Senior

UT Health San Antonio • San Antonio, TX

8d • Onsite

About The Position

Under limited supervision, responsible for planning, directing, and supervising complex administrative and fiscal functions of a unit directly engaged in research. May lead or mentor lower level team members.

Requirements

• Demonstrated knowledge in grant administration, research coordination, data collection, and/or facilitating the patient experience in research projects.
• Working knowledge with electronic health record systems and familiarity with medical terminology.
• Ability to coordinate the diverse components of the project by quality project planning, execution and change control to achieve required balance of time, cost and quality.
• Strong written and verbal communication skills to include the ability to generate high quality, technical writing and written/oral presentations.
• Proficient in using Microsoft Office (Word, Excel, PowerPoint) and databases.
• Detail oriented with meticulous planning, organizational and negotiating skills.
• CPR certification is required.

Nice To Haves

• Phlebotomy skills preferred.
• Knowledge in providing participant compensation and invoicing a study sponsor.
• Knowledge in grant administration, research coordination, data collection, and/or facilitating the patient experience in research projects.
• Knowledge with electronic health record systems and familiarity with medical terminology.
• Ability to coordinate the diverse components of the project by quality project planning, execution and change control to achieve required balance of time, cost and quality.
• Strong written and verbal communication skills to include the ability to generate high quality, technical writing and written/oral presentations.
• Proficient in using Microsoft Office (Word, Excel, PowerPoint) and databases.
• Familiarity with utilizing research portals, such as RedCap.
• Detail oriented with meticulous planning, organizational and negotiating skills.

Responsibilities

• Screens patients for protocol eligibility and participation in clinical trials.
• Participates in the coordination and monitoring of patient treatment.
• Monitors and evaluates patient response to protocol treatment in collaboration with the physician.
• Provides education regarding study activities to patient, relatives and other clinical staff as necessary per protocol.
• Processes human specimens per protocol including blood, urine, sputum, buccal swabs, etc.
• Prepares regulatory documents for Institutional Review Board and/or sponsor.
• Demonstrates competence to perform assigned responsibilities in a manner that meets the age specific and developmental needs of patients served by the department.
• Appropriately adapts assigned assessment and/or service methods to accommodate the unique physical, psychosocial, cultural, spiritual, age specific and other developmental needs of each patient served.
• Responsible for the complete administrative research process for a defined group to include pre/post award activities and regular communications and meetings with faculty and staff.
• Coordinates multiple research protocols and grant submissions; monitors budgets, spending, purchasing and participant payments.
• May conduct literature searches and assist with publications.
• Prepares and submits regulatory documents to the Institutional Review Board to obtain and maintain approval for research studies.
• Monitors ongoing activities to ensure compliance with local, state & federal regulations.
• Coordinates educational sessions and journal review meetings; collaborates to provide education and proctor/mentorship opportunities; may oversee the activities of student associates.
• Maintains research subject files for each study and enters all subject data into research database.
• Performs all other duties as assigned.

What This Job Offers

• Job Type: Full-time
• Career Level: Senior