Job Title : Clinical Trial Specialist
Job Description
As a Clinical Trial Specialist, you will be integral to the initiation, activation, and ongoing management of clinical trials.
You will collaborate with various departments to prepare and review study tools, verify necessary approvals, and translate finalized protocol treatment plans.
You will ensure timely prescreening of potential subjects, obtain informed consent, and provide backup support for patient registration.
Additionally, you will manage protocol-specific orders, coordinate patient care, and ensure accurate documentation. Your role will also involve grading adverse events, completing Serious Adverse Event forms, and supporting monitoring visits and audits.
You will maintain high standards of professional responsibility and performance, while staying current with continuing education and regulatory requirements.
Hard Skills
2-3 years clinical research coordination experience
1 year oncology required
Bachelor's degree in Nursing preferred
Experience with Oncore Study-start up task list
Experience in handling Case Report Forms (CRF) and database queries
Soft Skills
Collaboration
Effective communication
Problem-solving
Teamwork
Professional responsibility
Continuing education and skill building
Job Type
This is a Contract-to-Hire position with a duration of 12 Month(s).
Work Site
This is a hybrid position requiring some days on-site in New Brunswick, New Jersey and some days remote.
Work Environment
Our vision is to be a statewide, national, and world leader in scientific discovery, transdisciplinary engagement, translation, patient care, and education that improves outcomes for cancer patients and populations.
We achieve this through innovative research, patient-centered care, and education. The work environment includes clinical operations with disease-specific groups, research administration, quality assurance, informatics, education, and finance.
The team currently consists of 100 FTEs, with a goal of enrolling 5,000 subjects per year across multiple sites. The organization manages 300 active trials and aims to enroll 2,500 active subjects long-term, covering all phases of adult and pediatric trials.
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@ (%20actalentaccommodation@) for other accommodation options.
Compensation Information :
$0.0 / - $0.0 /
Starting At : 0.0
Up To : 0.0
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