CTMS Analyst (Remote)

WIRB-Copernicus Group

$73K — $114K *
US-AnywhereRemote in Cary, NC
Healthcare
Less than 5 years of experience
Job Overview by Ladders

Qualifications

  • Bachelor's degree preferred; equivalent experience considered.
  • Proven ability to thrive in a results-driven environment.
  • Strong understanding of clinical trial protocols and financial structures.
  • Experience in CTMS calendar builds and financial entry required.
  • Excellent organizational skills with strong attention to detail.
  • Strong investigative and critical thinking capabilities.
  • Effective verbal and written communication skills.

Responsibilities

  • Provide expert calendar builds and financial entries using clinical trial protocols.
  • Collaborate with teams to ensure alignment of budgets and agreements with protocols.
  • Revise deliverables accurately to reflect amendments and client changes.
  • Conduct internal quality reviews of work completed by team members.
  • Deliver exceptional customer service through effective communication and guidance.
  • Solve problems collaboratively with internal and site client teams.
  • Perform additional duties as directed by the supervisor.

Benefits

  • Opportunity to work remotely with a flexible schedule.
  • Supportive work culture focused on collaboration and communication.
  • Access to professional development and training opportunities.
  • Health and wellness benefits available to employees.
Full Job Description
General Information

Location: Cary, NC, Remote

Organization: PharmaSeek, LLC

Job Type: Full Time - Regular

Description and Requirements

The expected base salary range for this position is $73,350-$114,000. This salary range may vary based on the candidate's qualifications, experience, skills, education, and geographic location.

JOB SUMMARY: The CTMS Business Analyst is responsible for providing high-quality calendar builds and accurate financial entry services (service deliverables) for site clients who utilize a Clinical Trial Management System for clinical research financial oversight and patient enrollment management. WCG SSU services are culminated by the CTMS service deliverables, triggering the start date for site study activation. As such, timely and accurate CTMS service deliverables are imperative to meet the increasing demands on research sites to decrease study activation timelines, which directly affects site funding.

ESSENTIAL DUTIES/RESPONSIBILITIES:To perform this job successfully, an individual must be able to perform each essential duty and responsibility satisfactorily. The accountabilities listed below are representative of the knowledge, skills, and/or ability required.
  • Provide expert level calendar builds and financial entry utilizing industry expertise and incorporating site client requirements. Specific duties may vary depending on team assignments and business needs:
    • Read, analyze, and interpret clinical trial protocols to develop a comprehensive CTMS mapping plan.
    • Collaborate with internal WCG teams and site client to ensure billing determinations, sponsor budget, and clinical trial agreement are congruent with the clinical trial protocol and site client requirements prior to building calendar or entering financials in the CTMS platform.
    • Accurately revise previous deliverables to align with amendments and changing client preferences.
    • Review work completed by others as a part of the internal quality review process.
  • Manage site clients with exceptional customer service through industry expertise, guidance, and frequent communications.
  • Consultatively solve problems with internal WCG and site client teams to obtain consensus for best practices.
  • Other duties as assigned by supervisor. These may, on occasion, be unrelated to the position described here.
  • Attendance, time management and attendance are essential functions of the position.

EDUCATION REQUIREMENTS: Bachelor's degree in related field preferred. Equivalent combination of significant work experience in related field, education, and skills to perform the job may be considered in lieu of a relevant degree. Coverage analysis and research budget development experience preferred.

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.
  • Ability to work independently while providing a high-quality product within designated timelines.
  • Strong ability to read and interpret complex clinical trial protocols.
  • Prior experience with building calendars and entering financials into a CTMS platform.
  • Excellent attention to detail and highly organized.
  • Ability to understand clinical terms and descriptors and strong investigative and critical thinking skills.
  • Excellent communication (oral/written) and interpersonal skills.
  • Preferred but not required:
    • Familiarity with the clinical trial start-up process
    • Experience with oncology calendar builds and financial entry
    • Familiarity with research billing guidelines (e.g. Medicare NCD 310.1) and/or general healthcare billing processes (coding, Medicare regulations, etc.).

TRAVEL REQUIREMENTS:
• 0% - 5%

5% - 10%

10% - 20%

20% - 50%

>50%

Physical and Sensory Requirements: The physical and sensory requirements described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be offered to individuals with disabilities to assist in performing the essential functions of the position. Work activities involve light to moderate physical effort (for example, sitting in one place for extended periods of time, standing, walking, bending, lifting lightweight objects, intermittent to sustained periods of keyboarding). Majority of time is spent in a seated position with frequent opportunity to move about at will. Activities require a variety of easy muscle movements. Work activities involve a frequent need to concentrate on a variety of sensory inputs for moderate to lengthy durations at a time requiring diligence and attention to interpret effectively. There will be a need to attend to single or simultaneous tasks where accuracy of details is important. The need for detailed and precise work is high.

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