Summary:

Under the general supervision of the Principal Investigator(s) and Clinical Research Coordinator assist in recruitment acquisition and analysis of patient information for multiple clinical research projects.Interviews patients to gather information prepares and maintains study record enters data via computer performs statistical analyses of resultant data.Participates in qualitative/quantitative analyses of resultant data. Reviews relevant literature to gather information; may participate in development of research protocols.

Responsibilities:

Provides assistance to Principal Investigators to coordinate clinical research activities related to department�s field of study and investigators specific study.

Assists research clinician 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 questionnaire. 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.

Collects and organizes patient data into appropriate format to facilitate data entry.Operates computer to enter study information into database.

Collects processes and stores patient biospecimens including maternal hair urine saliva blood placenta and infant meconium saliva urine and cord blood.

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.

Other information:

BASIC KNOWLEDGE:

Bachelor�s Degree in Applied or Life Sciences or related area including courses in research methodologies and microcomputer systems.

EXPERIENCE:

Three to six months on-the-job experience to become familiar with specific research studies.

Knowledge of theory and techniques of research methodology.

Organizational skills to organize and prioritize own efforts on multiple projects and to gather research information format appropriately for computer data entry prepare and maintain records and reports etc.

Interpersonal skills to effectively interact with patients families and hospital professionals to gather and exchange information.

Analytical skills to participate in developing research protocols perform statistical analyses and participate in qualitative/quantitative analyses of research data.

Technical ability to operate and maintain computer system.

Demonstrated knowledge and skills necessary to provide care patients with consideration of aging processes human development stages and cultural patterns in each step of the care process.

WORK ENVIRONMENT AND PHYSICAL REQUIREMENTS:

Often works within a specific department to identify enroll and follow up with research patients.May spend much of the time standing and walking between departments offices Medical Records etc.

INDEPENDENT ACTION:

Perform independently within the department�s policies and practices.Refers specific complex problems to the supervisor when clarification of the departmental policies and procedures are required.

SUPERVISORY RESPONSIBILITY:

None.

Brown University Health is an Equal Opportunity employer. All qualified applicants will receive consideration for employment without regard to race color religion sex national origin age ethnicity sexual orientation ancestry genetics gender identity or expression disability protected veteran or marital status. Brown University Health is a VEVRAA Federal Contractor.

Location: The Miriam Hospital USA:RI:Providence

Work Type: Full Time

Shift: Shift 1

Union: Non-Union

The Miriam Hospital

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Clinical Research Assistant