Job Title: Clinical Trial Specialist

Job Description

As a Clinical Trial Specialist, you will be integral to the protocol activation process, ensuring the initiation and activation of new clinical trial protocols. This includes the preparation and review of study tools, verification of approvals, and collaboration with the Protocol Activation office. You will also be responsible for study accrual processes, including prescreening potential subjects, reviewing patient charts for eligibility, and obtaining informed consent in accordance with regulatory standards. Additionally, your clinical nursing responsibilities will involve direct patient care, protocol management, and coordination of interdisciplinary care to ensure adherence to treatment plans and protocol requirements. You will also maintain compliance with institutional, state, and federal regulations throughout the research project lifecycle and actively participate in continuous professional development.

Hard Skills2-3 years of experience as a clinical research coordinatorExperience with Oncore Study-start up task listProficiency in using computerized systems like Sunrise Disease/Clinical Manager, IDX, TDS, and Medical Records databaseExperience in handling Case Report Forms (CRF) and database queriesSoft SkillsStrong collaboration and communication skillsAbility to educate and train peersProactive problem-solving skillsDetail-oriented with strong organizational skillsJob 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

Join a visionary organization committed to being a leader in scientific discovery and patient care, aimed at improving outcomes for cancer patients. You will work in a dynamic setting alongside dedicated professionals, with a focus on cutting-edge patient-centered care and innovative research. The environment encourages transdisciplinary engagement and continuous learning, with a commitment to expanding our understanding of cancer and developing new therapies. Our team consists of 100 FTEs, operating in Newark and other sites across the state, actively managing 300 trials with a long-term goal of significantly increasing subject enrollment.

Please send your resume to gpacheco@ actalentservices.com if interested!

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.