Nurse Practitioner/Sub-Investigator

Tandem Intermediate LLC; Marrero (LA); On-site; USD 90,000 - 140,000; Full time

Job summary

Tandem Intermediate LLC is seeking a Sub-Investigator to join our clinical research team. The role combines direct medical care with patient education, ensuring high-quality trial conduct and patient safety.

As an advanced practice clinician, you will perform physical exams, interpret labs, administer investigational products, and collaborate with physicians and staff to advance clinical knowledge while maintaining strict regulatory compliance.

Qualifications

• Requires NP or PA licensure and clinical research experience.
• Strong phlebotomy and IV infusion skills with patient monitoring.
• Excellent communication and meticulous clinical documentation.

Responsibilities

• Perform physical examinations and assess patient medical histories.
• Interpret lab results and monitor patient health throughout the trial.
• Oversee patient safety and ensure protocol compliance.
• Educate patients and families on trial processes, risks, and care plans.
• Administer medications and oversee investigational product administration.
• Perform venipuncture and IV infusions as required by study protocols.
• Document clinical data in compliance with regulatory standards.
• Collaborate with the Principal Investigator and clinical trial team.

Skills

Phlebotomy

IV Infusion

Patient Monitoring

Clinical Research

Communication

Education

Nurse Practitioner License

Physician Assistant License

Tools

Phlebotomy equipment

Job description

About this position

Description:

The Sub-Investigator will serve as a key member of the clinical research team in a clinical trial setting. As an advanced practice medical professional, you will be responsible for ensuring the highest standards of patient care throughout the clinical trial process. Your primary role will involve conducting physical examinations, interpreting lab test results, overseeing patients’ health, and performing essential clinical procedures while working closely with other healthcare professionals. You will be expected to provide both direct medical care and education to patients, as well as contribute to the advancement of clinical knowledge through research and professional collaboration.

Key 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.
• Monitor and provide safety observations during and after medication or infusion administration to ensure patient well-being and manage any adverse reactions.
• Collaborate with the Principal Investigator and other members of the clinical trial team to ensure effective execution of study protocols.
• Ensure proper documentation of clinical data in accordance with regulatory and ethical standards.
• Maintain a clear, open line of communication with other healthcare professionals to ensure integrated, patient-centered care.
• Participate in regular meetings and discussions to review patient progress, study outcomes, and other relevant clinical findings.
• Stay informed on the latest developments in medical research and clinical practices, advancing personal and professional knowledge.

Additional Responsibilities

This job description includes core responsibilities but is not limited to the items listed above. The Sub-Investigator may be assigned additional duties as necessary to support the clinical trial and research efforts. These may include, but are not limited to, assisting in protocol design, supporting regulatory submissions, mentoring junior staff, and participating in educational and research initiatives.

Requirements:

License/Certification Requirements

• Nurse Practitioner Medical License or
• Physician Assistant License

Qualifications

• 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.

Preferred Skills

• Previous experience in clinical trials or research settings.
• Familiarity with regulatory guidelines and ethical practices in clinical research.
• Ability to educate patients and staff on clinical protocols and research procedures.