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Study Coordinator - Ophthalmology

Remote: 
Full Remote
Contract: 
Experience: 
Mid-level (2-5 years)
Work from: 
Texas (USA), United States

Offer summary

Qualifications:

Minimum 2 years in clinical research, Experience as Study Nurse/Coordinator, Completed degree in natural sciences, Knowledge of ICH-GCP Guidelines, Familiar with ophthalmology clinical studies.

Key responsabilities:

  • Oversee daily functions of clinical trials
  • Coordinate between staff, patients, and sponsors
  • Maintain adherence to FDA GCP/ICH guidelines
  • Manage subject study data accurately
  • Complete case report forms timely
TFS HealthScience - Contract Research Organization logo
TFS HealthScience - Contract Research Organization https://www.tfscro.com/
501 - 1000 Employees
See more TFS HealthScience - Contract Research Organization offers

Job description



  • TFS HealthScience is a leading global mid-size Contract Research Organization (CRO) that partners with biotechnology and pharmaceutical companies throughout their entire clinical development journey. Our expertise includes full service-capabilities, resourcing and Functional Service (FSP) solutions.

    Join Our Team as a Study Coordinator

    About This Role

    The Study Coordinator is responsible for coordination and supervision of clinical studies in various indications. This role will be the primary contact person for sponsors, potential clients and external service provider at clinics as well as for patients

    As part of our SRS team you will be dedicated to one of our partners. an emerging gene therapy company.

    This role will be onsite in Houston, Texas

    Key Responsibilities

    • Oversee daily functions of multiple clinical trials
    • Work with the Principal Investigator, site staff, patients, Sponsors.
    • Adhere to the guidelines of FDA GCP/ICH as well as study protocol and company SOPs.
    • Obtain informed consent under the guidance of the PI.
    • Coordinate patient visits from screening to follow up.
    • Ensure subjects meet all inclusion/exclusion criteria and have been properly consented prior to screening and enrolment into any clinical trial.
    • Coordinate, record and manage subject study data by maintaining accurate and complete source.
    • Complete case report forms and queries in a timely manner

    Qualifications

    • Minimum of 2 years relevant experience in clinical research or other healthcare environment
    • Professional experience as Study Nurse/Study Coordinator or completed full university degree in a natural science field
    • Experience in Ophthalmology
    • Good knowledge of ICH-GCP Guidelines
    • Good regulatory skills
    • Knowledge about clinical studies

    What We Offer

    We provide a competitive compensation package, comprehensive benefits, and the opportunity for personal and professional growth in a rewarding environment. You’ll be joining a team that values collaboration, innovation, and making a difference in the lives of patients

    A Bit More About Us

    Our journey began over 27 years ago in Sweden, in the city of Lund. As a full-service, global Contract Research Organization (CRO), we build solution-driven teams working towards a healthier future. Bringing together over 800 professionals, TFS delivers tailored clinical research services in more than 40 countries with flexible clinical development and strategic resourcing solutions across key therapeutic areas including Dermatology, Neuroscience, Oncology, and Ophthalmology.

    Our core values of Trust, Quality, Passion, Flexibility, and Sustainability are our guiding light serving as the framework for decision-making at all levels of the organization. They assist us in attracting and retaining valuable talent who share our sentiments, resulting in high employee engagement and satisfaction. By aligning on these fundamental values, we cultivate a unified force, geared towards innovation and excellence. This collective effort propels us towards our shared goal and fosters a culture of mutual respect and collaboration. Together we make a difference.

    Required profile

    Experience

    Level of experience: Mid-level (2-5 years)
    Spoken language(s):
    English
    Check out the description to know which languages are mandatory.

    Other Skills

    • Problem Solving
    • Natural Sciences
    • Verbal Communication Skills

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