REQUIRED WORK EXPERIENCE:

1) 2 years of clinical research experience or HS/AD with 1+ years of clinical research experience

PREFERRED WORK EXPERIENCE:

1) None Listed

SKILLS AND COMPETENCIES:

Seeks/completes additional research education and training.
Human Subjects Protection training (CITI) and any additional training as specified by the IRB prior to beginning any actual work on research protocols.
IATA certification is needed if job responsibilities include shipping of diagnostic specimens.
Develops/ maintains relationships with Sponsors, Colleagues, and BMC Departments
Knowledge of biology, chemistry, mathematics, documentation, and records management. Data utilization, complex problem solving, critical thinking, resource management, and writing skills.
Solid Computer Skills, including Databases.
A basic understanding of data collection and research principles is preferred.
May possess knowledge of medical terminology.
May possess working knowledge of State & Federal Regulations as they relate to research.
Highly detail-oriented individual with excellent interpersonal and time management skills.

EDUCATION:

GED or HiSET (Required)

1) Assists with moderately complex study tasks in accordance with protocol guidelines.
2) Performs Level I responsibilities with a higher level of problem resolution, analytical ability and self-direction.
3) Coordinate patient visits to the clinic. Organize study participant charts and files.
4) Collect required data from study coordinators and research nurses and enter it into clinical research forms and into a computerized database.
5) Generate letters to be sent to study participants.
6) Under the direction of the study coordinator or principal investigator, assist in enrolling patients in research studies. Contact patients as required after initial contact to obtain additional information.
7) Provide general clerical support to CRCs, sub-investigators, and investigators.
8) Order and maintain a log of stipend checks and/or gift certificates to be distributed to study participants.
9) Compile outreach packets, recruitment, and specimen collection kits
10) May have other responsibilities, including maintenance of refrigerator/freezer logs, inventory/ordering of study supplies, budget tracking, etc.
11) Contribute to the preparation, submission, and maintenance of regulatory documents.
12) Performs actual study tasks as directed.
13) Accurately compiles information and data.
14) May assist with sponsor/CRO visits.
15) Adheres to protocol, IRB, HIPAA, and regulatory requirements.