Description

\t\t\t\t\t

The PI agrees to assume the overall responsibility for the study conduct. By doing so, inherently agrees to:• Personally conduct or supervise the research• Ensure that each individual to whom a task is delegated is qualified by virtue of education, training, and experience to perform each of their delegated tasks• Protect the rights, safety and welfare of the participants who will be under their care. To do this they are agreeing that the research:o Is conducted in accordance with all federal regulatory requirements, state law and Pinnacle Clinical Research policies (including SOPs)o Is conducted in accordance with the IRB approved plano That they will ensure the accuracy, security and integrity of the research data and the subsequent analysis of that data. Duties and Responsibilities: • Review and hold expert knowledge of study related activities and protocols. • Assume all responsibilities and obligations as an Investigator, per Title 21 part 312 and FDA Form 1572.• Adhere to study protocols, FDA regulations, and Good Clinical Practice (GCP) at all times. • Maintain study sponsor and clinical trial confidentiality.• Performs study related procedures such as physical examinations, informed consent, subject history, adverse events, test article handling, appointment scheduling, records review, treatment coordination, collecting vital signs, and subject health assessments. Reviews and adjudicates all lab, imaging and biopsy findings. • Assists in the preparation for study monitor visits.• Performs subject screening and recruitment. • Provides some weekend coverage to facilitate study visits per protocol.• Provides after-hours phone call coverage as needed.• Oversee Sub-Investigators and recruitment team.

\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t

Additional Skills & Qualifications

\t\t\t\t\t

Summary: The Clinical Research Physician Investigator or PI is responsible for administering activities to facilitate clinical research and providing clinical support for the conduct and oversight of clinical trials•\tLicensed in Nevada•\tSomeone that can basically hit the ground running and has experience as a PI in pharma sponsored trials.•\tWill consider relo for the right candidate.•\tSalary $300k

\t\t\t\t\t

Experience Level

\t\t\t\t\t

Expert Level

Pay and Benefits

The pay range for this position is $300000.00 - $300000.00

Relocation assistance will be offered to Las Vegas location. Details to be negotiated though recruitment process.

Workplace Type

This is a fully onsite position in Las Vegas,NV.

Application Deadline

This position will be accepting applications until Jan 11, 2025.

About Actalent

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.

Diversity, Equity & Inclusion

At Actalent, diversity and inclusion are a bridge towards the equity and success of our people. DE&I are embedded into our culture through:

Hiring diverse talent Maintaining an inclusive environment through persistent self-reflection Building a culture of care, engagement, and recognition with clear outcomes Ensuring growth opportunities for our people

The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.

If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.