Clinical Research Specialist, Emergency Department
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
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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