Clinical Investigation Technician 2 Target Openings 40 Hour Rotating BWH Sleep Medicine

QUALIFICATIONS:

1.BS or BA in health science biology neuroscience psychology or related area or equivalent experience preferred.

2.College undergraduate course work. Prefer individuals with science or patientcare background and interest in scientific research.

3. Must be flexible to a work schedule involving day/evening/night/weekend shifts based on demands of the research protocols.

SKILLS/ ABILITIES/ COMPETENCIES REQUIRED:

1.Must possess good organizational and interpersonal skills.

2.Familiarity with Windowsbased computers required. Must be able to continually learn new computer skills and update existing skills.

3.Ability to maintain positive working relationships with coworkers and work cooperatively with peers.

4.Ability to work effectively as a member of a research team. Display initiative and sound judgment in crisis or unexpected situations. Take on additional work when required

5.Able to prioritize and manage time efficiently.

6.Ability to follow directions carefully and once trained to work with a minimum of direct supervision.

WORKING CONDITIONS:

During research studies nights overnights and weekend shifts will be required.

Busy laboratory environment. Occasional intense periods of work can be associated with particular scientific deadlines. May require the lifting carrying of specimens or supplies and the pushing pulling cart of specimens or supplies.

Potential exposure to bloodborne diseases through contact with biological specimens.

Brigham and Womens Hospital is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race sex color religion national origin sexual orientation protected veteran status or on the basis of disability.

GENERAL SUMMARY/ OVERVIEW STATEMENT:

The Medical Chronobiology Program investigates the mechanisms underlying the daily variation in disease severity including the morning peak in heart attacks and investigates the consequences of circadian disturbances such as in shift work.

Working under the supervision of a Research Manager or Principal Investigator and following established policies and procedures provides assistance on clinical research studies. May be responsible for the following activities: recruiting and evaluating subjects for studies; collecting organizing and analyzing research data; scheduling subjects for study visit; maintaining and updating data generated by the study while using specific equipment and assays during the inlaboratory portions of research protocols which will include combinations of day/evening/ night/weekend shifts.

PRINCIPAL DUTIES AND RESPONSIBILITIES:

Under the supervision of a Research Manager and/or Principal Investigator the Research Assistant will be responsible for protocols being carried out by the Medical Chronobiology Program in the Division of Sleep Medicine.

1.Provide assistance on clinical research studies as per study guidelines and protocols that will include combinations of day/evening/night/weekend shifts.

2.Recruit and evaluates potential study subjects per protocol guidelines. Per protocol instructions post advertisements for subject recruitment conducts telephone interviews and schedules patient for study visit and screening. May be required to perform clinical tests such as EKGs blood pressure measurement Hip Waist ratio etc.

3.Interact with patients/subjects with regard to study including patient education procedural instruction and followup.

4.Responsible for collecting data. May be required to input data do analysis and run various reports. Maintain subjects records as part of record keeping function.

5.Helps with mailing various study information or packets to study participants.

6.Answer any telephone calls and inquiries regarding study protocol. Refer study participants when appropriate to Research Manager and/or Principal Investigator.

7.Monitor and set up any needed equipment for study protocols.

8.Assists with performing measurements of several study parameters on human subjects while using specific equipment and assays during the inlaboratory portions of research protocols such as:

Noninvasive blood pressure and heart rate assessment from finger (Portapress) or brachial artery (Spacelabs) assessment of resting metabolic rate (Calorimeter) heart rate and blood pressure responses to changes in posture (Tilt Table Test) blood vessel function using noninvasive ultrasound (Brachial ultrasound) velocity of blood flow through the brain vessels (Transcranial Doppler) electrocardiography and having subjects perform exercise on treadmill and/or stationary bicycle (Exercise Tests).

9.Demonstrates professionalism and respect for subject rights and individual needs.

10.Collaborates with hospital personnel to ensure proper of research protocols.

11.Monitors supplies and equipment necessary to conduct protocols.

12.Performs all other functions in order to complete research protocols. May be requested to assist investigators in the preparation of IRB amendments and continuing reviews SOPs progress reports grant proposals and manuscripts as needed.

13.Coordinates inlab visits:

a. Responsible for coordinating the inpatient staffing arrangements of the research studies for which you are the primary recruiter. This includes working with the Principal Investigator Project Leader Division staff CCI staff and the study candidates to schedule studies.

b. Ensure proper equipment and procedures are in place before a study to monitor data quality and monitor procedural adherence on a regular basis.

14.May be responsible for maintaining and organizing freezers.

15.May be responsible for coordinating and planning meetings and Journal Clubs taking notes and making agendas.

16.May be responsible for maintaining equipment and supplies and serving as the contact for outside vendors and training entities.

17.Arranges and sends out blood samples when needed.

18.Performs other duties as required.