Nurse Practitioner (Clinical Research)
55–75 an hour
Behavioral Health Market Context
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Job Description
and accessible. They focus on on large-volume recruitment and retention of diverse and specialty patient populations, and have an experienced team with extensive physician partnerships help deliver high-quality data across a wide range of therapeutic areas!
The Role
The Sub-Investigator (Clinical Research NP) is responsible for oversight and execution of clinical trials that test new medications on the behalf of sponsor/pharmaceutical companies. You will work in an oncology clinic to promote Good Clinical Practice and follow research protocols assigned alongside the PI. You will work along a lead Physician (Principal Investigator) have a team of skilled coordinators, managers, and assistants as well.
• Evaluate and screen potential subjects based on study eligibility criteria
• Perform and review medical procedures in accordance with the clinical study protocol
• Complete all documentation, paper and electronic
• Provide oversight and ensures proper delegation of duties to appropriate staff
• Provide and maintain updated study related documentation
• Evaluate and report safety reports, protocol noncompliance and any other protocol specific reports.
• Medical management of patients on trial
• Administering medications including IV
• Tracking and management of adverse events
• Monitoring
Qualifications
• Board Certified Nurse Practitioner
• Ability to dedicate a full time schedule on site in Chesterfield, MO
• Prior experience working in Clinical Research
The Role
The Sub-Investigator (Clinical Research NP) is responsible for oversight and execution of clinical trials that test new medications on the behalf of sponsor/pharmaceutical companies. You will work in an oncology clinic to promote Good Clinical Practice and follow research protocols assigned alongside the PI. You will work along a lead Physician (Principal Investigator) have a team of skilled coordinators, managers, and assistants as well.
• Evaluate and screen potential subjects based on study eligibility criteria
• Perform and review medical procedures in accordance with the clinical study protocol
• Complete all documentation, paper and electronic
• Provide oversight and ensures proper delegation of duties to appropriate staff
• Provide and maintain updated study related documentation
• Evaluate and report safety reports, protocol noncompliance and any other protocol specific reports.
• Medical management of patients on trial
• Administering medications including IV
• Tracking and management of adverse events
• Monitoring
Qualifications
• Board Certified Nurse Practitioner
• Ability to dedicate a full time schedule on site in Chesterfield, MO
• Prior experience working in Clinical Research
Qualifications
- •Board Certified Nurse Practitioner
- •Ability to dedicate a full time schedule on site in Chesterfield, MO
- •Prior experience working in Clinical Research
Benefits
- •$55 - $75/hr based on experience and qualifications
- •Monday - Friday 8am - 4pm schedule
Responsibilities
- •Work on Research studies in Neurology, Pulmonology, Endocrinology, and Vaccine!
- •The Sub-Investigator (Clinical Research NP) is responsible for oversight and execution of clinical trials that test new medications on the behalf of sponsor/pharmaceutical companies
- •You will work in an oncology clinic to promote Good Clinical Practice and follow research protocols assigned alongside the PI
- •You will work along a lead Physician (Principal Investigator) have a team of skilled coordinators, managers, and assistants as well
- •Evaluate and screen potential subjects based on study eligibility criteria
- •Perform and review medical procedures in accordance with the clinical study protocol
- •Complete all documentation, paper and electronic
- •Provide oversight and ensures proper delegation of duties to appropriate staff
- •Provide and maintain updated study related documentation
- •Evaluate and report safety reports, protocol noncompliance and any other protocol specific reports
- •Medical management of patients on trial
- •Administering medications including IV
- •Tracking and management of adverse events
- •Monitoring