Clinical Research Specialist, Emergency Department

Beth Israel Lahey Health

Burlington, VTFull-time

Behavioral Health Market Context

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Job Description

 supervision and guidance to Clinical Research Coordinators. May serve as a project manager or team lead with supervisory responsibilities. Performs diverse duties requiring analysis, sound judgment and a high level of knowledge of specific protocols. Maintains interdisciplinary relationship with participating physicians and clinical departments. Interacts with study participants diagnosed with various medical conditions and diagnoses.

Responsibilities
• coordinating multiple research studies by implementing study protocols in accordance with regulatory, departmental and institutional requirements
• Provides mentoring, direction, supervision and guidance to Clinical Research Coordinators
• May serve as a project manager or team lead with supervisory responsibilities
• Performs diverse duties requiring analysis, sound judgment and a high level of knowledge of specific protocols
• Maintains interdisciplinary relationship with participating physicians and clinical departments
• Interacts with study participants diagnosed with various medical conditions and diagnoses

Requirements
• Bachelor’s degree required; Master’s degree preferred. 5+ years of relative experience. In absence of a Bachelor’s degree, will consider 8+ years of relevant work experience in addition to the experience noted below.
• 5+ years of direct work-related experience in a research setting; proven leadership ability and ability to successfully work independently with little to no direction; proven ability to comprehend and apply regulations
• Strong verbal and written communication, multi-tasking, attention to detail, organizational and leadership skills
• Proven ability to function independently, set priorities, take direction and initiative
• Ability to travel nationally to other research sites, attend investigator meetings and educational conferences as required
• Ability to communicate clearly and effectively and work collaboratively in small teams
• Ability to act as a team leader creating a collaborative and respectful team environment and improving workflows
• Ability to provide a high level of customer service to patients, colleagues, professional staff and external contacts to offer ideas, identify issues, obtain information or deliver services
• Ability to interact with study participants with various diseases compassionately and respectfully
• In the absence of any of these skills, demonstrates the ability to be thoroughly trained to meet organizational standards

Nice-to-haves
• CCRP/CCRC Certification, or equivalent certification, preferred.
• supervisory experience a plus
• Epic experience a plus

Qualifications

  • 5+ years of relative experience
  • In absence of a Bachelor’s degree, will consider 8+ years of relevant work experience in addition to the experience noted below
  • 5+ years of direct work-related experience in a research setting; proven leadership ability and ability to successfully work independently with little to no direction; proven ability to comprehend and apply regulations
  • Strong verbal and written communication, multi-tasking, attention to detail, organizational and leadership skills
  • Proven ability to function independently, set priorities, take direction and initiative
  • Ability to travel nationally to other research sites, attend investigator meetings and educational conferences as required
  • Ability to communicate clearly and effectively and work collaboratively in small teams
  • Ability to act as a team leader creating a collaborative and respectful team environment and improving workflows
  • Ability to provide a high level of customer service to patients, colleagues, professional staff and external contacts to offer ideas, identify issues, obtain information or deliver services
  • Ability to interact with study participants with various diseases compassionately and respectfully
  • In the absence of any of these skills, demonstrates the ability to be thoroughly trained to meet organizational standards

Benefits

    Responsibilities

    • Functioning independently with minimal supervision and direction, will be responsible for coordinating multiple research studies by implementing study protocols in accordance with regulatory, departmental and institutional requirements
    • Provides mentoring, direction, supervision and guidance to Clinical Research Coordinators
    • May serve as a project manager or team lead with supervisory responsibilities
    • Performs diverse duties requiring analysis, sound judgment and a high level of knowledge of specific protocols
    • Maintains interdisciplinary relationship with participating physicians and clinical departments
    • Interacts with study participants diagnosed with various medical conditions and diagnoses
    • coordinating multiple research studies by implementing study protocols in accordance with regulatory, departmental and institutional requirements
    • Provides mentoring, direction, supervision and guidance to Clinical Research Coordinators
    • May serve as a project manager or team lead with supervisory responsibilities
    • Performs diverse duties requiring analysis, sound judgment and a high level of knowledge of specific protocols
    • Maintains interdisciplinary relationship with participating physicians and clinical departments
    • Interacts with study participants diagnosed with various medical conditions and diagnoses


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