Website Talent Software Services, Inc.
Talent Software Services, Inc.
Company : Talent Software Services, Inc.
This position is 100% onsite and offers an opportunity to contribute to impactful clinical research projects. The role requires a combination of clinical research coordination and administrative skills to ensure the smooth execution of research studies.
Required Qualifications
Associates Degree
3 years of experience as a Clinical Research Coordinator (CRC)
1 year of experience in Oncology
Basic Life Support (BLS) certification
Proven longevity in previous roles
Interest in transitioning from temporary to permanent employment
Preferred Qualifications
Bachelors Degree
SoCRA or ACRP Certification
Phlebotomy Certification
Medical Assistant Diploma
Primary Duties and Responsibilities
Establish and execute logistical aspects of clinical research projects to achieve objectives, including project planning, resource projection, and developing systems for protocol compliance and patient safety.
Coordinate administrative functions of research studies, including scheduling patient research visits, procedures, and labs, and maintaining consent forms, case report forms, SAE’s, and source documents.
Screen and recruit potential patients for protocol eligibility, present non-medical trial concepts to patients, and support the informed consent process.
Ensure accurate and timely data collection, documentation, entry, and reporting, including resolving queries from sponsors or regulatory entities.
Coordinate institutional, pharmaceutical, and internal audits, facilitate third-party study monitoring, and implement corrective actions as needed.
Compile and report on study information, including protocol activity, accrual data, workload, and other research information; present findings at regular research staff meetings.
Submit adverse events, serious adverse events, protocol deviations, and Safety Letters in accordance with local and federal guidelines in a timely manner.
Identify quality and performance improvement opportunities and collaborate with staff to develop action plans for improvement.
Plan and coordinate strategies to increase research participant enrollment and improve clinical research efficiency.
Provide technical support for grant proposals, publications, presentations, and special projects.
Assist with research project budget development, including identifying and classifying routine care vs. research-related care, and assist with research participant billing and reconciliation.
Attend meetings and conferences related to research activities, including research staff meetings.
Participate in planning, workshops, evaluation meetings, seminars, educational or administrative meetings as necessary or requested.
Participate in training and education of new research personnel.