Clinical Research Associate II – Full Service, ONC, Gen Med
Syneos Health
Google Cloud Platform
Senior Field Clinical Research Specialist – RDN
Medtronic
full-time
Posted on:
Location Type: Remote
Location: Remote • Colorado, Missouri • 🇺🇸 United States
Visit company websiteSalary
💰 $108,000 - $162,000 per year
Job Level
Senior
Tech Stack
Google Cloud Platform
About the role
- Provide technical and educational support to physicians globally
- Responsible for clinical trial site management, case coverage, and clinical trial data tracking
- Select sites, perform activation duties, set up protocols, provide training, help enroll participants, support cases, ensure quality data acquisition and perform study closure activities
- Maintain frequent contact with principal investigators, sub-investigators, and research coordinators
- Gain and maintain knowledge of clinical sites to understand and assess investigators' interests and capabilities
- Continuous communication to in-house clinical trial leaders regarding the status and performance of multiple studies
- Assist in the successful conduct of assigned clinical studies consistent with applicable regulations, guidelines, and policies
- Interface with representatives from key functional groups
- Identify and mitigate quality risks and issues for assigned clinical studies
- Oversee follow-up and resolution of site issues
- Assist in control of device allocation, distribution and reconciliation
- Assist with oversight of activities performed by Contract Research Organizations (CROs)
Requirements
- Bachelor’s degree with 4+ years of clinical research/clinical (e.g. field clinical research/clinical specialist/field clinical engineer) experience OR Advanced degree with 2 years of clinical research/clinical (e.g. field clinical research/clinical specialist/field clinical engineer) experience
- Hospital/clinical experience
- Experience in Good Clinical Practice (GCP) and regulatory compliance guidelines for clinical trials
- Certification from a Clinical Research Association (CCRP/CCRC)
- Experience at Medtronic or within the medical device industry
- Experience in the management of clinical devices
- Cardiovascular/cardiac rhythm management device training (e.g., pacemakers & defibrillators)
- Experience in a Cath lab, biomedical engineering, hospital/clinic or medical sales
- Experience in clinical studies and/or trial site management/protocols
- Experience collaborating with cross functional clinical partners/customers, physicians and/or medical sales colleagues in the healthcare industry
Benefits
- Health, Dental and vision insurance
- Health Savings Account
- Healthcare Flexible Spending Account
- Life insurance
- Long-term disability leave
- Dependent daycare spending account
- Tuition assistance/reimbursement
- Simple Steps (global well-being program)
- Incentive plans
- 401(k) plan plus employer contribution and match
- Short-term disability
- Paid time off
- Paid holidays
- Employee Stock Purchase Plan
- Employee Assistance Program
- Non-qualified Retirement Plan Supplement (subject to IRS earning minimums)
- Capital Accumulation Plan (available to Vice Presidents and above, or subject to IRS earning minimums)
Applicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard skills
clinical trial managementdata trackingprotocol setupquality data acquisitionclinical researchGood Clinical Practice (GCP)regulatory complianceclinical device managementcardiovascular device trainingtrial site management
Soft skills
communicationcollaborationproblem-solvingorganizational skillsinterpersonal skills
Certifications
Clinical Research Association Certification (CCRP/CCRC)
