Physician Assistant / Nurse Practitioner Sub-Investigator
Behavioral Health Market Context
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Job Description
ntribute to advancing medical science by promoting diversity in clinical trial research and ensuring high-quality, patient-centered research.
Practice Info
• Clinical research site located in Maplewood, MN
• Conducts clinical research trials involving pulmonology and respiratory care, sleep, endocrine, metabolic, obesity, and general medicine
• Led by Dr. Charlene McEvoy
• Strategically located in a diverse metro area that is home to vibrant communities, including Somali, Hmong, Latino, African American, and Native American populations
• Partners with pharmaceutical sponsors and CROs
Responsibilities
• Ensure the safety and welfare of each study subject
• Have in-depth knowledge of all research protocols
• Screen potential study subjects according to the protocol's specific inclusion and exclusion criteria
• Conduct medical history interviews and physical examinations throughout the subject's study participation
• Review EKG's and lab results
• Provide medical care as needed during a subject's participation in a clinical trial
• Provide home based on-call availability per Artemis standard policy
• Attend Investigator Meetings on behalf of Principal Investigator as needed
Compensation
• Competitive and dependent upon years of experience as an Investigator in clinical research
Shift & Schedule
• Full-time Regular Employee
• Mondays through Fridays, 8:00am-5:00pm
• Onsite in Maplewood, MN (no opportunities for remote or hybrid)
Requirements
• Minimum of two years of experience as a licensed physician assistant, family or non-acute adult nurse practitioner treating a wide variety of therapeutic areas for the adult and geriatric patient population required (internal medicine, family medicine, urgent care, emergency medicine)
• Current and unencumbered license to practice as an NP or PA in the state of Minnesota required
• Prior experience within the clinical research industry highly preferred
• Commitment and ability to deliver excellent customer service
• Excellent communication, punctual and responsible
• Extremely well organized
• Excellent verbal and written communication skills
• Trustworthy, reliable; attentive to details
• Mature and pleasant demeanor
• Willingness to learn new tasks and grow with the company
Practice Info
• Clinical research site located in Maplewood, MN
• Conducts clinical research trials involving pulmonology and respiratory care, sleep, endocrine, metabolic, obesity, and general medicine
• Led by Dr. Charlene McEvoy
• Strategically located in a diverse metro area that is home to vibrant communities, including Somali, Hmong, Latino, African American, and Native American populations
• Partners with pharmaceutical sponsors and CROs
Responsibilities
• Ensure the safety and welfare of each study subject
• Have in-depth knowledge of all research protocols
• Screen potential study subjects according to the protocol's specific inclusion and exclusion criteria
• Conduct medical history interviews and physical examinations throughout the subject's study participation
• Review EKG's and lab results
• Provide medical care as needed during a subject's participation in a clinical trial
• Provide home based on-call availability per Artemis standard policy
• Attend Investigator Meetings on behalf of Principal Investigator as needed
Compensation
• Competitive and dependent upon years of experience as an Investigator in clinical research
Shift & Schedule
• Full-time Regular Employee
• Mondays through Fridays, 8:00am-5:00pm
• Onsite in Maplewood, MN (no opportunities for remote or hybrid)
Requirements
• Minimum of two years of experience as a licensed physician assistant, family or non-acute adult nurse practitioner treating a wide variety of therapeutic areas for the adult and geriatric patient population required (internal medicine, family medicine, urgent care, emergency medicine)
• Current and unencumbered license to practice as an NP or PA in the state of Minnesota required
• Prior experience within the clinical research industry highly preferred
• Commitment and ability to deliver excellent customer service
• Excellent communication, punctual and responsible
• Extremely well organized
• Excellent verbal and written communication skills
• Trustworthy, reliable; attentive to details
• Mature and pleasant demeanor
• Willingness to learn new tasks and grow with the company
Qualifications
- •Minimum of two years of experience as a licensed physician assistant, family or non-acute adult nurse practitioner treating a wide variety of therapeutic areas for the adult and geriatric patient population required (internal medicine, family medicine, urgent care, emergency medicine)
- •Current and unencumbered license to practice as an NP or PA in the state of Minnesota required
- •Commitment and ability to deliver excellent customer service
- •Excellent communication, punctual and responsible
- •Extremely well organized
- •Excellent verbal and written communication skills
- •Trustworthy, reliable; attentive to details
- •Mature and pleasant demeanor
- •Willingness to learn new tasks and grow with the company
Benefits
- •Strategically located in a diverse metro area that is home to vibrant communities, including Somali, Hmong, Latino, African American, and Native American populations
- •Competitive and dependent upon years of experience as an Investigator in clinical research
- •Full-time Regular Employee
- •Mondays through Fridays, 8:00am-5:00pm
- •Onsite in Maplewood, MN (no opportunities for remote or hybrid)
Responsibilities
- •This role involves conducting clinical research trials across various therapeutic areas, including pulmonology, respiratory care, sleep, endocrine, metabolic, obesity, and general medicine
- •The successful candidate will contribute to advancing medical science by promoting diversity in clinical trial research and ensuring high-quality, patient-centered research
- •Conducts clinical research trials involving pulmonology and respiratory care, sleep, endocrine, metabolic, obesity, and general medicine
- •Partners with pharmaceutical sponsors and CROs
- •Ensure the safety and welfare of each study subject
- •Have in-depth knowledge of all research protocols
- •Screen potential study subjects according to the protocol's specific inclusion and exclusion criteria
- •Conduct medical history interviews and physical examinations throughout the subject's study participation
- •Review EKG's and lab results
- •Provide medical care as needed during a subject's participation in a clinical trial
- •Provide home based on-call availability per Artemis standard policy
- •Attend Investigator Meetings on behalf of Principal Investigator as needed
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