Nurse Practitioner/Physician Assistant Sub-Investigator
Somers Point, NJFull-time
Behavioral Health Market Context
Apply Nowvia Marit Health
Job Description
fessionals to advance clinical knowledge.
Practice Info
• Clinical trial setting
Responsibilities
• Perform physical examinations and assess patients' medical histories in a clinical trial setting.
• Interpret and analyze lab test results to monitor patient health and make clinical decisions.
• Oversee and monitor patient health status throughout the trial, ensuring patient safety and compliance with protocol requirements.
• Educate patients and their families on the clinical trial process, including treatment plans and potential risks.
• Administer medications and oversee the safe administration of investigational products, ensuring adherence to clinical protocols.
• Perform venipuncture and phlebotomy procedures for laboratory testing as required by study protocols.
• Prepare, initiate, and monitor IV infusions (including investigational product infusions), ensuring safe administration, accurate documentation, and appropriate patient monitoring.
• Conduct medical procedures such as IV line placement, injections, and other tasks as required by the study protocol.
Requirements
• Nurse Practitioner Medical License or Physician Assistant License
• Proven experience in a clinical or healthcare setting, with a focus on patient care and medical research.
• Strong phlebotomy and IV infusion skills, with demonstrated competency in patient monitoring during and after procedures.
• Strong problem-solving skills and the ability to make sound clinical decisions.
• Excellent communication skills, with the ability to effectively interact with patients, families, and other healthcare professionals.
• Detail-oriented with a commitment to accuracy in medical documentation and patient monitoring.
• Team player with a positive attitude and dedication to advancing clinical knowledge and patient care.
• A strong passion for clinical research, patient advocacy, and advancing medical practices.
Practice Info
• Clinical trial setting
Responsibilities
• Perform physical examinations and assess patients' medical histories in a clinical trial setting.
• Interpret and analyze lab test results to monitor patient health and make clinical decisions.
• Oversee and monitor patient health status throughout the trial, ensuring patient safety and compliance with protocol requirements.
• Educate patients and their families on the clinical trial process, including treatment plans and potential risks.
• Administer medications and oversee the safe administration of investigational products, ensuring adherence to clinical protocols.
• Perform venipuncture and phlebotomy procedures for laboratory testing as required by study protocols.
• Prepare, initiate, and monitor IV infusions (including investigational product infusions), ensuring safe administration, accurate documentation, and appropriate patient monitoring.
• Conduct medical procedures such as IV line placement, injections, and other tasks as required by the study protocol.
Requirements
• Nurse Practitioner Medical License or Physician Assistant License
• Proven experience in a clinical or healthcare setting, with a focus on patient care and medical research.
• Strong phlebotomy and IV infusion skills, with demonstrated competency in patient monitoring during and after procedures.
• Strong problem-solving skills and the ability to make sound clinical decisions.
• Excellent communication skills, with the ability to effectively interact with patients, families, and other healthcare professionals.
• Detail-oriented with a commitment to accuracy in medical documentation and patient monitoring.
• Team player with a positive attitude and dedication to advancing clinical knowledge and patient care.
• A strong passion for clinical research, patient advocacy, and advancing medical practices.
Qualifications
- •Nurse Practitioner Medical License or Physician Assistant License
- •Proven experience in a clinical or healthcare setting, with a focus on patient care and medical research
- •Strong phlebotomy and IV infusion skills, with demonstrated competency in patient monitoring during and after procedures
- •Strong problem-solving skills and the ability to make sound clinical decisions
- •Excellent communication skills, with the ability to effectively interact with patients, families, and other healthcare professionals
- •Detail-oriented with a commitment to accuracy in medical documentation and patient monitoring
- •Team player with a positive attitude and dedication to advancing clinical knowledge and patient care
- •A strong passion for clinical research, patient advocacy, and advancing medical practices
Benefits
Responsibilities
- •As a Sub-Investigator, you will be a vital member of the clinical research team, dedicated to upholding the highest standards of patient care throughout clinical trials
- •This role involves conducting physical examinations, interpreting lab results, and performing essential clinical procedures
- •You will provide direct medical care and patient education, while collaborating with other healthcare professionals to advance clinical knowledge
- •Perform physical examinations and assess patients' medical histories in a clinical trial setting
- •Interpret and analyze lab test results to monitor patient health and make clinical decisions
- •Oversee and monitor patient health status throughout the trial, ensuring patient safety and compliance with protocol requirements
- •Educate patients and their families on the clinical trial process, including treatment plans and potential risks
- •Administer medications and oversee the safe administration of investigational products, ensuring adherence to clinical protocols
- •Perform venipuncture and phlebotomy procedures for laboratory testing as required by study protocols
- •Prepare, initiate, and monitor IV infusions (including investigational product infusions), ensuring safe administration, accurate documentation, and appropriate patient monitoring
- •Conduct medical procedures such as IV line placement, injections, and other tasks as required by the study protocol
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