SUMMARY: Under general supervision, but following established policies and procedures, performs scientific investigative research in areas related to patient care. Researches literature in the field, participates in the design of experimental protocols and develops new procedures to carry out established research objectives. Interviews patients to gather information, prepares and maintains study record, enters data via computer,. Participates in the qualitative/quantitative analyses of data. May assist in writing presentations and papers for publication based on the research performed. May perform EKG’s and take vital signs during research-based monitoring tests. May also perform blood spinning and shipment of blood and tissue samples as required by protocol.
Brown University Health employees are expected to successfully role model the organization's values of Compassion, Accountability, Respect, and Excellence as these values guide our everyday actions with patients, customers and one another. In addition to our values, all employees are expected to demonstrate the core Success Factors which tell us how we work together and how we get things done. The core Success Factors include: Instill Trust and Value Differences Patient and Community Focus and Collaborate RESPONSIBILITIES:
Provides assistance to Principal Investigators to coordinate clinical research activities related to Department of Geriatrics field of study and investigators specific study. Assists research physician in identification and follow up of patients meeting criteria for inclusion in clinical research studies; ensures protocol eligibility requirements are met. Establishes and/or maintains study record for each participant. Interviews patient and/or family to explain nature of study, elicit cooperation and gather information to complete study questionnaires and other study procedures. Facilitates obtaining informed consent. May schedule patient appointments and call patients to complete documentation. May review medical records to abstract information necessary to complete forms. May request and follow up on missing data such as laboratory test results and the like. Monitors adherence to protocol; alerts physician when laboratory tests ordered have not been performed, medication protocol not followed, etc. May perform research-based EKG’s, vital signs, blood spinning and shipping of blood and tissue products, in accordance with protocol specifications. Collects and organizes patient data into appropriate format to facilitate data entry. Operates computer to enter study information into database. Using pre-packaged software and according to needs of research supervisor, performs computer-assisted statistical analysis such as multiple antecedent variables, linear regression, frequencies, cross tabulations and the like. May write non-complex programs using computer and software –compatible language to reformat information, create new files, etc. Maintains computer equipment, arranges for internal/external service as necessary to effect repairs and maintenance. Prepares related graphs and charts or results of data gathered. Participates in quantitative and qualitative analyses of resultant information. May assist in planning research protocols. Coordinates activities of others assigned to research project to interview patients, compete forms or perform other tasks. Reviews literature pertaining to research being conducted in order to better understand project and gather relevant information. Any other duties as required. Hours may vary to meet study requirements and some on call duty (evening, weekends and overnights) may be required.
MINIMUM QUALIFICATIONS: BASIC KNOWLEDGE: Bachelor’s Degree in Applied or Life Sciences or related area, . EXPERIENCE: Two to three years progressively more responsible and related experience in the clinical research field. Experience should demonstrate effective working knowledge of research methodology and an in-depth knowledge of the scientific field in which the research is being conducted. SUPERVISORY RESPONSIBILITY: Provides functional guidance to subordinate research staff assigned to the project. Job location will include a laboratory environment with possible exposure to human and animal serum chemical reagents, animal subjects and radioactive materials.
*Location states RIH however locations vary based on the needs of the projects and may include RIH, TMH, East Providence Outpatient clinic, Nursing Homes throughout the state of Rhode Island and patient homes. Use of reliable vehicle required
Pay Range:
$48,068.80-$79,372.80EEO Statement:
Brown University Health is committed to providing equal employment opportunities and maintaining a work environment free from all forms of unlawful discrimination and harassment.
Location:
Rhode Island Hospital - 593 Eddy Street Providence, Rhode Island 02903Work Type:
Typically, M-F 7-3:30 but applicant must be flexible adn work different hours or very occasional weekend hours to meet study goals,Work Shift:
DayDaily Hours:
8 hoursDriving Required:
YesSkills Required
- Bachelor's Degree in Applied or Life Sciences or related area
- Two to three years progressively responsible clinical research experience demonstrating research methodology and field knowledge
- Ability to perform EKGs and take vital signs and to process (spin) and ship blood and tissue samples per protocol
- Experience interviewing patients, obtaining informed consent, and abstracting medical record data
- Computer skills including data entry, use of study databases, basic statistical analysis, and ability to write simple programs/scripts
- Ability to work variable hours and occasional on-call shifts including evenings, weekends, or overnights as study requires
- Use of a reliable vehicle / driving required for travel to multiple site locations
- Willingness/ability to work in laboratory environment with possible exposure to human and animal serum, chemical reagents, animal subjects and radioactive materials
