Sacred Heart University
and the job listing Expires on January 16, 2026
Our fast paced, dynamic research group is looking fan exceptional Research Assistant to join our team. We are one of the leading private sites for research in Dermatology in the country and offer excellent opportunities for growth. As a group, we believe in investing in our employees, developing their skills and facilitating their potential . The ideal candidate will be a medical assistant or certified phlebotomist, with research experience and will posses the essential skills and abilities listed below. We offer a competitive salary and benefits with room for growth within the company.
Under general supervision, the Clinical Research Assistant aids the CRC in patient visits and all protocol associated requirements including to but not limited to collecting and entering clinical data, sample collection, processing and shipment, administrative tasks, patient recruitment, advertising, patient database management.
Essential Skills and Abilities
Ability to understand and follow basic scientific research protocols and procedures and complex detailed technical instructions with detailed accuracy
Proficiency and adaptability with technology: Excel, Word, PowerPoint, Outlook and database management, experience with Electronic Data Capture (EDC), Interactive Voice/Web Response System (IVRS/IWRS) and Clinical Trial Management Software (CTMS) systems a plus
Flexible and composed demeanor in a fast paced setting with the ability to interact effectively with all levels of management and staff
Exceptional organizational, interpersonal and multitasking skills
Responsibilities
Aids in collecting, documenting and logging clinical research data according to the study protocol, sponsor guidelines and FDA requirements
Collects, processes, and ships clinical specimen per protocol and IATA guidelines
Performs administrative tasks, including but not limited to all protocol requirements for patient visits, scheduling patient visits, obtains medical records as needed and fulfills study drug accountability requirements
Assisting in the setup, operation and maintenance of research equipment/instruments
Aids in basic clinical evaluations including blood pressure, pulse and EKGs, reviews current and changes to medications and documents adverse events
Supports the preparation of presentations and scientific publications as needed
Supports the overall goals of the company
Performs other related duties
Education and Experience #J-18808-Ljbffr
Our fast paced, dynamic research group is looking fan exceptional Research Assistant to join our team. We are one of the leading private sites for research in Dermatology in the country and offer excellent opportunities for growth. As a group, we believe in investing in our employees, developing their skills and facilitating their potential . The ideal candidate will be a medical assistant or certified phlebotomist, with research experience and will posses the essential skills and abilities listed below. We offer a competitive salary and benefits with room for growth within the company.
Under general supervision, the Clinical Research Assistant aids the CRC in patient visits and all protocol associated requirements including to but not limited to collecting and entering clinical data, sample collection, processing and shipment, administrative tasks, patient recruitment, advertising, patient database management.
Essential Skills and Abilities
Ability to understand and follow basic scientific research protocols and procedures and complex detailed technical instructions with detailed accuracy
Proficiency and adaptability with technology: Excel, Word, PowerPoint, Outlook and database management, experience with Electronic Data Capture (EDC), Interactive Voice/Web Response System (IVRS/IWRS) and Clinical Trial Management Software (CTMS) systems a plus
Flexible and composed demeanor in a fast paced setting with the ability to interact effectively with all levels of management and staff
Exceptional organizational, interpersonal and multitasking skills
Responsibilities
Aids in collecting, documenting and logging clinical research data according to the study protocol, sponsor guidelines and FDA requirements
Collects, processes, and ships clinical specimen per protocol and IATA guidelines
Performs administrative tasks, including but not limited to all protocol requirements for patient visits, scheduling patient visits, obtains medical records as needed and fulfills study drug accountability requirements
Assisting in the setup, operation and maintenance of research equipment/instruments
Aids in basic clinical evaluations including blood pressure, pulse and EKGs, reviews current and changes to medications and documents adverse events
Supports the preparation of presentations and scientific publications as needed
Supports the overall goals of the company
Performs other related duties
Education and Experience #J-18808-Ljbffr