This job is closed
Applications are no longer available for this announcement. Explore current related opportunities below.
Job description
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.
PI70c294d
Who can apply
Review the original listing for work authorization, qualifications and employer requirements.