Responsibilities

Coordinate, evaluate, and perform the nursing care of participants and collect data for assigned research projectsMaintain skills in clinical competencies such as physical assessment, phlebotomy, and IV insertionReview all elements of the current institutional IRB approved informed consent document with study candidates and/or legal representativesEnsure patient advocacy and informed consent as an ongoing process, prioritizing the rights, safety, and well-being of trial subjectsManage multiple clinical trial protocols, coordinate the execution and follow-up of each protocol, and perform accurate, legible, and timely documentationManage records, study medication, and test articles in a confidential and secure mannerPromote PI oversight by advising the PI, sub-investigator(s), Supervisor, and/or Clinical Operations Manager of deviations in conduct, patient status, and issues relevant to the integrity of the trial and/or the safety of research subjectsCoordinate the work of support staff, laboratory technicians, and assistants to ensure efficient, timely, and high-quality results and adherence to research protocols

 

Qualifications

Must have a minimum of 2 years of Clinical Research experience within the Oncology therapeutic OR 2 years of Oncology bedside nursing experienceAssociate degree in NursingCurrent, active State of FL license as a Registered NurseBLS certificationDemonstrate skills in clinical competencies, including physical assessment, phlebotomy, IV insertion, and administration of investigational drugs

 

Shift

Monday-Friday 8 am-4:30 /5pm, based on the needs of the business

Pay and Benefits

The pay range for this position is $75000.00 - $98000.00

Benefits from Day One

Paid Days Off from Day One

Career Development

Whole Person Wellbeing Resources

Mental Health Resources and Support

Pet Insurance*

Debt-free Education* (Certifications and Degrees without out-of-pocket tuition expense)

Workplace Type

This is a fully onsite position in Orlando,FL.

Application Deadline

This position will be accepting applications until Jan 2, 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.