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Tandem Intermediate LLC logo

Nurse Practitioner/Sub-Investigator

Tandem Intermediate LLC·Viera, Florida

$120,000 - $135,000/yr·Full Time·On Site·2-5 yrs·Posted 4 months ago
Practice for this role

About the role

The Sub-Investigator provides direct medical care and oversight for patients within a clinical trial setting, including performing physical exams and administering investigational products. They collaborate with the Principal Investigator to ensure protocol compliance and accurate documentation of clinical data.

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.

Posting details

Employment type
Full Time
Work arrangement
On Site
Experience
2-5 yrs
Salary
$120,000 - $135,000/yr
Location
Viera, Florida
Posted
Mar 6, 2026
Application
Employer website
Tandem Intermediate LLC logo

Hiring organization

Tandem Intermediate LLC

Tandem Clinical Research is a multi-therapeutic, independent and dedicated clinical research site. Our team has conducted more than 350 trials in phases I-IV. Our trained and dedicated staff works diligently to provide you with timely and accurate data. With clinics in Marrero...

Salary listed on 1 job
IndustryResearch Services
TypePrivately Held
Size11-50 employees
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Market context

Florida advanced-practice roles stay competitive

In Florida, advanced-practice roles typically see steady demand in settings that need licensed Nurse Practitioners with broad patient-care skills. These positions are competitive because employers often look for board certification, current BLS, and experience with both adult and pediatric IV therapy, while benefits such as medical, dental, vision, disability coverage, and tuition reimbursement can strengthen an offer. Review the AI-summarized requirements and benefits here to save time, then confirm your license, certification, and pediatric/adult care experience match the posting before applying.

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