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Clinical Trial Specialist

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Actalent

3mo ago

  • Job
    Full-time
    Junior & Mid Level
  • Research & Development
    Healthcare
  • Edison

AI generated summary

  • You need 2-3 years as a clinical research coordinator, experience with Oncore, proficiency in Sunrise/IDX/TDS, CRF handling, strong communication, training skills, and attention to detail.
  • You will prepare and review study tools, verify approvals, prescreen subjects, review eligibility, obtain consent, provide patient care, and ensure compliance with regulations throughout the trial.

Requirements

  • 2-3 years of experience as a clinical research coordinator
  • Experience with Oncore Study-start up task list
  • Proficiency in using computerized systems like Sunrise Disease/Clinical Manager, IDX, TDS, and Medical Records database
  • Experience in handling Case Report Forms (CRF) and database queries
  • Strong collaboration and communication skills
  • Ability to educate and train peers
  • Proactive problem-solving skills
  • Detail-oriented with strong organizational skills

Responsibilities

  • 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.

FAQs

What is the duration of the Clinical Trial Specialist position?

The position is a Contract-to-Hire with a duration of 12 months.

Where is the work site for this position?

This is a hybrid position requiring some days on-site in New Brunswick, New Jersey, and some days remote.

What are the essential hard skills required for this role?

Candidates should have 2-3 years of experience as a clinical research coordinator, experience with Oncore Study-start up task list, proficiency in using computerized systems like Sunrise Disease/Clinical Manager, IDX, TDS, and Medical Records database, and experience in handling Case Report Forms (CRF) and database queries.

What soft skills are important for the Clinical Trial Specialist position?

Strong collaboration and communication skills, the ability to educate and train peers, proactive problem-solving skills, and being detail-oriented with strong organizational skills are important for this role.

What kind of work environment can I expect as a Clinical Trial Specialist?

You will work in a dynamic setting alongside dedicated professionals, with a focus on cutting-edge patient-centered care and innovative research in an organization committed to improving outcomes for cancer patients.

Is continuous professional development encouraged in this role?

Yes, the position emphasizes continuous professional development.

How many trials does the team actively manage?

The team actively manages 300 trials with a long-term goal of significantly increasing subject enrollment.

Will I have direct patient care responsibilities?

Yes, direct patient care is part of the clinical nursing responsibilities for this position.

Who should I contact if I am interested in this position?

Interested candidates should send their resume to gpacheco@actalentservices.com.

Does Actalent promote diversity and inclusion in the workplace?

Yes, Actalent is committed to diversity, equity, and inclusion as integral components of their culture.

What should I do if I need a reasonable accommodation during the application or interview process?

You can request a reasonable accommodation by emailing actalentaccommodation@actalentservices.com for other accommodation options.

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Actalent

An Engineering and Sciences Services Company | People to Possible

Human Resources
Industry
5001-10,000
Employees

Mission & Purpose

Actalent connects passion with purpose. Our scalable talent solutions and services capabilities drive value and results and provide the expertise to help our customers achieve more. Every day, our experts around the globe are making an impact. We’re supporting critical initiatives in engineering and sciences that advance how companies serve the world. Actalent’s global footprint and flexible delivery models ensure access to specialized talent where and when you need it. We promote consultant engagement through professional development and provide experiences to ensure continuous learning. Our people are the difference. Our expertise spans capabilities in engineering including product and manufacturing, systems and software, construction management, environmental, architecture and civil; and power and utilities. We focus on sciences capabilities in laboratory sciences, healthcare, and clinical research. Actalent is an operating company of Allegis Group, the global leader in talent solutions.