Sr Clinical Research Assistant

Brown Medicine•Cranston, RI

2d•$48,069 - $79,373•Onsite

About The Position

Under general supervision and in accordance with established policies and procedures, performs scientific investigative research related to patient care. Research activities include reviewing relevant literature, participating in the design of experimental protocols, and developing methods to meet research objectives. The role interviews patients, maintains study records, enters and analyzes data, and participates in qualitative and quantitative analyses. It may also involve assisting with presentations and publications, performing EKGs and taking vital signs during research monitoring, and processing and shipping blood and tissue samples as required by protocol. The position may provide functional guidance to subordinate research staff assigned to the project. Work is at Rhode Island Hospital, 593 Eddy Street, Providence, Rhode Island. The schedule is Monday through Friday, 8:30 a.m. to 5:00 p.m., with an eight-hour workday. Driving is not required. The laboratory environment may involve exposure to human and animal serum, chemical reagents, animal subjects, and radioactive materials. Brown University Health employees are expected to role model the values of Compassion, Accountability, Respect, and Excellence and demonstrate the Success Factors of Instill Trust and Value Differences, Patient and Community Focus, and Collaborate.

Requirements

Bachelor’s degree in applied or life sciences, or a related area, including coursework in research methodologies and microcomputer systems.
Two to three years of progressively more responsible, related experience in the research field.
Experience demonstrating effective working knowledge of statistics, computer programming, and research methodology.
In-depth knowledge of the scientific field in which the research is conducted.

Responsibilities

Identify patients who meet clinical research study inclusion criteria and verify protocol eligibility requirements.
Participate with the research investigator in designing experimental protocols to meet research objectives.
Develop research methodologies within the parameters of protocols and objectives to support quantitative and qualitative evaluation and interpretation of data.
Establish and maintain study records; interview patients or family members, explain the study, gather information, and facilitate informed consent.
May schedule patient appointments and contact patients to complete documentation.
Review medical records and abstract information; request and follow up on missing data, including laboratory test results.
Monitor adherence to study protocols and alert physicians to issues such as unperformed laboratory tests or failure to follow medication protocols.
Collect and organize patient data, enter data, and create, modify, and maintain study databases.
Tabulate, graph, chart, and analyze data using statistical methods, including computer-assisted analyses such as linear regression, frequencies, and cross-tabulation.
Write non-complex computer programs to reformat information and create files.
Participate in qualitative and quantitative analysis and interpretation of study results with the principal investigator and other research professionals; may recommend protocol modifications based on initial findings.
May provide functional guidance to subordinate research staff, clarify protocol requirements, help resolve issues, and support their professional development in interpreting statistical trends.
May assist in writing presentations and papers for publication based on research performed.
Review relevant literature and maintain and enhance professional expertise through educational opportunities and participation in related teams and conferences.
May perform research-based EKGs, take vital signs, spin blood, and ship blood and tissue products in accordance with protocol specifications.