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Clinical Research Associate

Remote: 
Full Remote
Contract: 
Full time
Experience: 
Mid-level (2-5 years)
Work from: 
United States

Offer summary

Qualifications:

Bachelor's degree in scientific discipline or healthcare preferred, At least 2 years of on-site monitoring experience, 2-3 years of in-house or remote monitoring experience, Medical device clinical trials experience desirable, In-depth knowledge of GCP and ICH guidelines.

Key responsabilities:

  • Conduct site qualification, initiation, and close-out visits
  • Monitor compliance with clinical trial protocols and regulations
  • Train site staff and manage study-related documentation
  • Coordinate investigator recruitment and obtain regulatory approval
  • Serve as primary contact between RQM+, sponsor, and investigator
RQM+ logo
RQM+ SME https://www.rqmplus.com/
501 - 1000 Employees
About RQM+
RQM+ is the leading MedTech service provider with the world’s largest global team of regulatory and quality experts. Building upon 40 years of regulatory expertise, we also provide comprehensive clinical trial, lab and reimbursement services – reducing risk and supporting market access throughout the entire product lifecycle for medical devices, digital therapeutics and diagnostics. With more former FDA, Medicines and Healthcare Products Regulatory Agency (MHRA) and notified body regulators than any other firm, the RQM+ team has deep expertise in all clinical specialties. RQM+ currently works for 19 of the top 20 medical device manufacturers and seven of the top 10 IVD companies.
See more RQM+ offers

Job description

 RQM+ is the leading MedTech service provider with the world’s largest global team of regulatory and quality experts. Building upon 40 years of regulatory expertise, we also provide comprehensive clinical trial, lab and reimbursement services – reducing risk and supporting market access throughout the entire product lifecycle for medical devices, digital therapeutics and diagnostics. With more former FDA, Medicines and Healthcare Products Regulatory Agency (MHRA) and notified body regulators than any other firm, the RQM+ team has deep expertise in all clinical specialties. RQM+ currently works for 19 of the top 20 medical device manufacturers and seven of the top 10 IVD companies.

The Clinical Research Associate (CRA) participates in the preparation and execution of pre-market to post market clinical trials. Oversees the progress of clinical investigations by conducting site qualification, initiation, and interim close out visits to clinical sites. Monitors clinical trials in accordance with Good Clinical Practices and procedures set forth by RQM+ and sponsors. Works closely with the Clinical Trial Manager (CTM) and/or Lead CRA to ensure all monitoring activities are conducted according to study requirements.

Primary Responsibilities
  • Participates in the investigator recruitment process and performs site qualification visits of potential investigators.
  • Evaluates the capability of the site to successfully manage and conduct the clinical study.
  • Collaborates with the start-up department to coordinate activities with the site in preparation for the initiation of the study.
  • Obtains regulatory documentation for successful implementation, monitoring, and evaluation of clinical trials.
  • Works with start-up, project team and site staff to obtain regulatory (IRB/IEC) approval of study specific documents.
  • Performs study initiation activities, reviewing with the site personnel the protocol, regulatory issues, study procedures, and provides training on completion of the eCRF, monitoring activities and study close-out activities.
  • Trains site staff on the EDC system and verifies site computer system.
  • Assists in resolving any issues to ensure compliance with site file audits in conjunction with ISS.
  • Assures adherence to Good Clinical Practices, investigator integrity, and compliance with all study procedures through on-site monitoring visits.
  • Performs validation of source documentation as required by sponsor and prepares monitoring reports and letters per the timelines defined in RQM+ SOPs by using approved templates and reports.
  • Documents accountability, stability and storage conditions of clinical trial materials as required by sponsor.
  • Performs investigational or commercial product inventory and accountability (as applicable)
  • Ensures return of unused study product to designated location or verifies destruction as required.
  • Reviews the quality and integrity of the clinical data through in-house review of electronic CRF data and on-site source verification.
  • Works with sites to resolve data queries.
  • May review protocols, eCRFs, study manuals and other related documents, as requested by the Clinical Trial Manager and/or Lead CRA.
  • Serves as primary contact between RQM+, sponsor and investigator; coordinates all correspondence; ensures timely transmission of clinical data with the study site and technical reporting, as requested.
  • Performs study close-out visits per the study specific Clinical Monitoring Plan including final study product reconciliation and disposition, site study file reconciliation, data query resolution through to database lock and resolution of outstanding action items.
  • Assists with, and attends, Investigator Meetings for assigned studies.
  • Authorized to request site audits due to data integrity concerns.
  • Attends study-related, company, departmental, and external meetings, as required.
  • Ensures internal and study-related trainings are completed per RQM+ process and/or study timelines, including updating the study level trial management system.
  • Ensures all study deliverables are completed per RQM+ and study timelines.
  • Serves as mentor for junior staff and those new to the company and/or study.
  • Performs other duties, as requested

    • Requirements
  • Bachelor's Degree in scientific discipline or health care preferred.
  • Requires at least 2 years of year of on-site monitoring experience.
  • 2-3 years in-house or remote monitoring experience
  • Medical Device clinical trials experience is highly desirable
  • Equivalent combination of education, training and experience considered
  • In-depth knowledge of, and skill in applying, applicable clinical research regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines. MedTech regulations and active experience preferred.
  • Strong therapeutic and protocol knowledge as provided in company training.
  • Computer skills including proficiency in the use of Microsoft Word, Excel and PowerPoint and use of a laptop computer and mobile technology required.
  • Written and verbal communication skills including command of English language.
  • Organizational and pragmatic problem-solving skills
  • Effective time and financial management skills
  • Ability to establish and maintain effective working relationships with coworkers, managers, sponsor staff and sites.
  • Ability to travel up to 50%

    • Behaviours
  • Action-Oriented, Approachability, Building Effective Teams, Business Acumen, Career Ambition, Composure, Courage (Managerial), Customer Focus, Decision Quality, Informing, Integrity & Trust, Interpersonal Savvy, Planning

    • Supervisory Responsibilities
  • This position does not have supervisory responsibilities.
    • Being an industry leader in Medtech is just the beginning for RQM+. We consider our employees our biggest asset and we invest heavily in ongoing learning and development. Providing a rewarding place to work is rooted deep in our core values. From an industry leading compensation package to a deeply engrained focus on work life balance, RQM+ has a unique offering for regulatory and quality professionals. At RQM+, you are not just another employee, you are a member of RQM+ family. Make your impact today! 

    We invite you to apply if you have an interest in learning more about our organization and beginning your journey with us.


    Job Opportunity Verification
    At RQM+, we prioritize the security of our job applicants. To ensure a safe application process:
    All legitimate RQM+ job opportunities are listed on our official careers page: rqmplus.com/careers
    Every candidate going through the interview process will participate in a voice and/or video interview.
    Exercise caution with unsolicited job offers or requests for sensitive information.

    Required profile

    Experience

    Level of experience: Mid-level (2-5 years)
    Spoken language(s):
    EnglishEnglish
    Check out the description to know which languages are mandatory.

    Hard Skills

    Educational TherapyMedical DevicesOnline CommunicationDecision ScienceProject CollaborationData VerificationClinical ResearchRegulatory DocumentsCareer DevelopmentFinancial ManagementCustomer CentricityGood Clinical Practices (GCP)Application MonitoringFDA Regulations

    Other Skills

    • Courage
    • Motivational Skills
    • Relationship Management
    • Microsoft PowerPoint
    • Composure
    • Trustworthiness
    • Planning
    • Organizational Skills
    • Business Acumen
    • Microsoft Word
    • Non-Verbal Communication
    • Microsoft Excel
    • Time Management
    • Social Intelligence
    • Training And Development
    • Action Oriented
    • Team Building
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