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Cordis · 1 month ago

Senior Field Specialist, Clinical Research (Remote/National Travel)

United States

Full-time

Remote

Mid, Senior Level

$76K/yr - $145K/yr

3+ years exp

Cordis, in partnership with Selution, specializes in revolutionary healthcare technology for treating coronary and peripheral artery diseases. The Senior Field Specialist, Clinical Research role involves providing case support to physicians, conducting training, and ensuring quality data acquisition for clinical studies in a designated territory.

Health CareHealth DiagnosticsMedical

No H1B

Responsibilities

Perform Physician and hospital staff training and procedural case coverage to ensure safe and effective use of the device

Present clinical study training materials based on investigational plans including study protocol, IFU, core lab manuals and case report forms

Provide field support for clinical studies by participating in site selection, site initiation and activation, supporting cases, ensuring quality data acquisition throughout follow up and performing study closure activities

Address clinical research site needs by maintaining frequent contact via email/phone/on-site visits with PI's and research coordinators

Responsible for gaining and maintaining knowledge of clinical sites in a given geographical area to best understand and assess investigators interests and capabilities

Manage key study sites (investigators and research staff) and serve as 'live' point of contact with the site for communication with SELUTION CSM, CRA, and CRO team

Partner with SELUTION clinical research teammates to meet business needs in the field including site CIP questions, re-training, case coverage, data entry/query resolution and escalation of critical issues

Administrative activities including evaluating metrics, data entry into trackers, documentation of activities and site feedback to SELUTION study teams

Assist with overall successful conduct of assigned clinical studies consistent with applicable regulations, guidelines and policies

Identify and mitigate quality risks and issues for assigned clinical studies with oversight from study management team

Assist with oversight of activities performed by CRO

Maintain in-depth knowledge of current study protocols, process and procedures to assist sites and facilitate study management team efforts

Qualification

Clinical research experienceCardiovascular proceduresTrainingEducationCoronary interventionsPeripheral interventionsCommunication skillsTeam collaborationProblem-solving

Required

Ability to travel 75%+ within designated geographic territory

Minimum 3 years' experience with cardiovascular procedures in clinical research in this same role or as a nurse or tech as radiology tech or Cath lab tech

Minimum 3 years' experience working directly with physicians and healthcare professionals

Experience in coronary or peripheral interventions

Ability to travel (at least 75%) to company and clinical trial sites