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28 days old

Clinical Research Analyst

WIRB-Copernicus Group (WCG)

General Information

Location: Cary, NC, Madison, WI

Organization: PharmaSeek, LLC

Job Type: Full Time - Regular

Description and Requirements

SUMMARY OF POSITION: The Clinical Research (CR) Analyst is responsible for assisting research institutions with budget development and negotiation, coverage analysis, and clinical trial management system services. The Clinical Research Analyst will complete these critical functions in a manner designed to expedite the conclusion of the start-up process for our clients while maintaining a high level of quality.

VACCINATION REQUIREMENT:

To be considered for U.S.-based positions unless currently employed by WCG, where permitted by applicable law (including any applicable reasonable accommodation, medical or religious exemption), candidates must have received or be willing to receive the COVID-19 vaccine by start date.

EDUCATION REQUIREMENTS:

       Bachelors degree or higher in Science, Mathematics, or another related field.

QUALIFICATIONS/EXPERIENCE:

  • Ability to work in a performance-driven environment: a proactive, results-driven and goal-oriented approach.
  • Demonstrated ability to learn and apply technical and scientific product-related information in a consultative manner.
  • Excellent attention to detail and highly organized.
  • Ability to understand clinical terms and descriptors and strong investigative skills with ability to think outside the box.
  • Excellent communication (oral/written) and interpersonal skills.
  • Proficient in Microsoft Office.

ESSENTIAL DUTIES/RESPONSIBILITIES: To perform this job successfully, an individual must be able to perform each essential duty and responsibility satisfactorily. The requirements listed below are representative of the knowledge, skills, and/or ability required.

  • Develop coverage analysis for clinical trials (50%).
    • Read and analyze clinical trial protocols to identify required tests/procedures.
    • Code each procedure per the applicable CPT/HCPCS coding guidelines.
    • Interpret Medicare policies to determine what procedures are billed to the sponsor and which are billed to Medicare/private insurance.
    • Identify appropriate research modifiers to be placed on claims.
  • Build comprehensive clinical trial budgets based on clients preferred pricing methodologies (20%).
  • Negotiate clinical trial budgets on behalf of research institutions (20%).
  • Build protocols within clients clinical trial management system (5%).
  • Other duties as assigned by supervisor. These may, on occasion, be unrelated to the position described here (5%).

SUPERVISORY RESPONSIBILITIES: None.

TRAVEL REQUIREMENTS: None.


IND123
Posted: 2021-08-26 Expires: 2021-09-27

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Clinical Research Analyst

WIRB-Copernicus Group (WCG)

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