Company

Swedish AmericanSee more

addressAddressRockford, IL
type Form of workFull-Time
CategoryEducation/Training

Job description

POSITION SUMMARY:

To support the implementation and management of clinical trials research at UW-Health NIL/SwedishAmerican. This includes but is not limited to: thorough and accurate trial subject data collection and entry into appropriate computer software; coordination of molecular and genomic testing; assists in maintaining research subject files; coordination of and assistance with monitoring visits; assists in maintaining protocol files; administrative support to the Research team.

EDUCATION/TRAINING:

Bachelor’s degree preferred with a preferred focus in biology, health science, or related fields.

LICENSURE/CERTIFICATION:

Certified Clinical Research Professional (CCRP), Certified Clinical Research Associate (CCRA), or Certified Clinical Research Coordinator (CCRC) preferred; other certifications may be considered

EXPERIENCE/SKILLS/ABILITIES:

Must be proficient in using Microsoft Office programs, database setup and management, and the use of electronic medical records. Excellent problem-solving, organizational, and communication skills (includes verbal and written communication) are required. Must be detail oriented and have the ability to work in a fast-paced environment with multiple, simultaneous projects and deadlines. Must be self-motivated and able to work independently. Successful candidates must demonstrate dependability, flexibility, and maturity. Candidates must be effective at building interpersonal relationships with constructive interactions, be clear and effective communicators, promote and create collegial environments that value accountability.

ESSENTIAL FUNCTIONS:

  • Works as a part of research team to collect, abstract, and interpret subject data from the medical record and subject themselves. Records and enters data as outlined in protocol. Resolves data queries and verifies the accuracy of all data.
  • Creates and maintains study protocol files, ensuring all documents are up to date and accurate.
  • Follows all applicable organizational, state, and federal policies and regulations governing human subject research. Performs quality reviews and audits as necessary.
  • As a part of the Research Team, coordinates and facilitates sponsor monitoring visits.
  • Serves as the point of contact for molecular and genomic testing conducted at facility. Includes receipt of orders, initiation of testing, entering information using online portals, monitoring for results, and sending results to provider. Serves as liaison between facility and testing companies.
  • Provides administrative support to Research Team, which may include but is not limited to creation of and updating department standards of practice; development of standard work for Research related processes; requesting and receiving specimen kits; assists with annual applications and recertification as necessary.
  • Other responsibilities as assigned.
  • Our Commitment to Diversity, Equity, and Inclusion

    UW Health is committed to being a diverse, inclusive and anti-racist workplace and is an Equal Employment Opportunity, Affirmative Action employer. Our integrity shines through in patient care interactions and our daily work practices as we work to embrace the knowledge, unique perspectives and qualities each employee and faculty member brings to work each day. Applications from Black, Indigenous and People of Color (BIPOC) individuals, LGBTQ+ and non-binary identities, women, persons with disabilities, military service members and veterans are strongly encouraged. EOE, including disability/veterans.


    PI234327838

    Refer code: 7771313. Swedish American - The previous day - 2024-01-08 13:22

    Swedish American

    Rockford, IL
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