Clinical Trial Administrator

Company: Quotient Sciences

  • Location: Miami, United States
  • Seniority: Mid level
  • Employment type: Full-time
  • Posted: Yesterday
  • Offer language: English

Job description

Quotient Sciences: Molecule to Cure. Fast.

Quotient Sciences is a leading drug development and manufacturing accelerator, helping biotech and pharma companies bring new medicines to patients faster. With over 35 years of experience and a track record of success, we provide Drug Product (CDMO) and Clinical (CRO) services across the entire development pathway, including formulation development, clinical pharmacology, clinical trials, and commercial product manufacturing.

Our proprietary and disruptive platform – “Translational Pharmaceutics®” – integrates Drug Product Manufacturing and Clinical Testing to eliminate silos in the drug development process. This in turn reduces costs, improves outcomes, and significantly accelerates drug development times.

Why Join Us

Because every day counts when bringing new medicines to patients. Our 1,000+ experts across the US, UK, and beyond are united by science, agility, and a culture that turns ideas into impact—fast.

The Role

  • The Clinical Trial Administrator, is responsible to provide administrative support for the Project Management group and to lead the study review activities and communications on allocated projects
  • To comply & adhere to GCP guidelines and regulations as required of this role

Main Tasks And Responsibilities

  • Assist in the preparation and formatting of study documentation, including but not limited to informed consent forms, source documents, and client deliverables.
  • Investigator Site File and eTMF set up and maintenance
  • Complete and initiate TMF QC (paper and electronic)
  • Set up and filing into client Trial Master Files (electronic or paper) where requested by clients
  • Maintain delegation logs by coordinating with internal teams to ensure accuracy and timely updates for new and terminated staff.
  • Maintain training logs and ensure training compliance for all personnel listed on delegation logs.
  • Manage file note control, including creation, review, and filing.
  • Ensure all regulatory documentation is audit-ready and compliant with archiving requirements.
  • Support study review board submissions by uploading administrative documents, study updates, and required correspondence.
  • Process Spanish regulatory documents and communicate approvals to the screening team.
  • Notify staff of updated or newly released documents via secure file systems.
  • Assist with study closeout activities, including archiving.
  • Maintain and perform quality control (QC) of the volunteer clinical RSVP database.
  • Manage laboratory requisitions and collaborate with Data Management to support query resolution.
  • Support eSource User Acceptance Testing (UAT) activities.
  • Set up of admission binders
  • Breakdown of files ready for archiving
  • Assists with all other duties as assigned
  • Assist with the hosting and support of sponsor monitors during site visits and with related action items

Job Demands

The Job May Involve The Following

  • Very high concentration of work
  • Strict and tight deadlines
  • Having to juggle a range of tasks/issues simultaneously
  • Working in a hazardous environment with high requirement to follow safety procedures
  • Working outside normal working hours
  • Needing to respond to client demands

The Candidate

  • High School Diploma or equivalent
  • Relevant work experience in a pharmaceutical company/CRO would be an advantage
  • Computer literate, proficient in Microsoft Windows
  • Proficient in Information Technology
  • Highly organized and efficient
  • Ability to communicate effectively; people-oriented personality

Application Requirements

When applying for a position with Quotient Sciences to be able to work in our organization you must be aged 18 years or over and not have been debarred by the FDA. If you indicate you are under the age of 18 or have been debarred then your application will be automatically declined.

Our Commitment to Diversity, Equity and Inclusion

Quotient Sciences are advocates for positive change and conscious inclusion. We strive to create a diverse Quotient workforce and develop a workplace culture that provides a sense of acceptance for every person within our organization. As a global employer, we recognize the value in having an organization that is a true reflection and representation of our society today.

Specifically we will not discriminate on the basis of race, color, creed, religion, gender, gender identity, pregnancy, marital status, partnership status, domestic violence victim status, sexual orientation, age, national origin, alienage or citizenship status, veteran or military status, disability, medical condition, genetic information, caregiver status, unemployment status or any other characteristic prohibited by federal, state and/or local laws.

This applies to all aspects of employment, including hiring, promotion, demotion, compensation, training, working conditions, transfer, job assignments, benefits, layoff, and termination.

Our Approach to AI in Recruitment

At Quotient Sciences, we use technology, including AI-enabled tools, to support parts of our recruitment process and help create an efficient, consistent, and inclusive candidate experience. Any use of AI is subject to human oversight, and hiring decisions are made by people, not technology.

While we embrace innovation, our recruitment process remains deeply human. Candidates who progress through our recruitment process are supported by a dedicated recruitment contact, and many of our selection processes include in-person interviews. We believe the best hiring decisions come from real conversations, giving candidates the opportunity to meet future colleagues, experience our culture and showcase their strengths beyond their application.

We recognize that candidates may choose to use AI tools when preparing applications. We encourage the responsible use of technology to support research, preparation, and drafting. However, applications should reflect your own skills, experiences, and perspectives. Throughout the recruitment process, we assess authenticity, critical thinking, technical capability, and the unique contribution you can bring to Quotient Sciences. Content generated entirely by AI may not provide an accurate representation of your suitability for the role.

Courses that can help you get this job

Similar offers

  • Clinical Trial Associate

    €7,060–7,800 / month

    Company: Cardurion Pharmaceuticals

    Offer language: English Posted:Today
    • Location: Burlington, United States
    • Seniority: Mid level
    • Employment type: Full-time
  • Company: Infotree Global Solutions Agency

    Offer language: English Posted:Today
    • Location: California, United States
    • Work mode: Remote
    • Seniority: Mid level
    • Employment type: Contract
  • Company: ICON Strategic Solutions

    Offer language: English Posted:Today
    • Location: Miami, United States
    • Seniority: Senior
    • Employment type: Full-time
  • Sr. Clinical Research Associate

    €7,430–9,660 / month

    Company: CareDx, Inc.

    Offer language: English Posted:Today
    • Location: Brisbane, United States
    • Work mode: Remote
    • Seniority: Senior

Get Started. It's FREE

Fill out the form to get started today for FREE: Access all features and preview up to 5 courses of your choice for 2 weeks!

Register

Get started today for FREE: Access all features and preview up to 5 courses of your choice for 2 weeks!

A password will be sent to your email address.

By requesting free demo, you confirm that you have read and understood the privacy policy and you agree to receive marketing communications from AIDIFY regarding product updates, offers, and insights. You can unsubscribe at any time.