Clinical Trial Participant Recruitment Selection Coordinator, Bank Contract, Leeds
3 weeks ago
As a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access and technology solutions across more than 20 therapeutic areas. With over 19,000 staff conducting operations in more than 90 countries, Fortrea is transforming drug and device development for partners and patients across the globe.
As one of the largest Clinical Research Organizations in the world, we have recently brought to life four ultramodern Clinical Research Units in the UK and US… and the jewel in the crown is our facility at Drapers Yard Leeds . A brand new, world class, state-of-the-art 65,000 ft² clinic with 100 beds (and growing), fully dedicated to Phase I Clinical research (and 7 minutes walking from the train station)
And this is where you come in because we are expanding and now seeking our next Clinical Trial Participant Recruitment Selection Coordinator.
You will need to be able to commit to working 5 out of 7 days per week (usually Mond to Fri), but also be open to shift work, including twilight, nights and weekends. This means you will have the you may not be guaranteed these hours every week as these
WHY IS THIS A SPECIAL OPPORTUNITY?
You will gain a profound insight into how clinical trials are executed as you will:
Interact with multiple departments Witness firsthand clinical research as it is being conducted in real time.When the drug you worked with gets approved, you know you´ll touch many patient´s lives around the world.
Support us on our mission “To help make life-changing healthcare solutions possible”. Apply now and be part of an extraordinary journey.
ON A NORMAL DAY, YOU WILL…
You will support our teams in their participant recruitment efforts, ensuring the correct eligibility of participants in the right clinical trial. You will:
Be the focal point preparing and collating complex and diverse screening data coming to you from different teams, and Communicate this to the appropriate group (from physicians to pathologists or study managers), to ensure the accurate and fast selection of subjects for specific studies.As the person acting as a central hub of subjects´ information and for answering questions within Fortrea and from clients, you will:
Streamline the daily process of gathering & presenting participants´ laboratory results and collating screening data to physicians for medical review and acceptance of subjects for study. Determine the panel of eligible and standby subjects for specific studies after receiving completed data from the physicians. Conduct daily QC of screening Case Report Forms (CRF). Maintain exquisite documentation and accurate record keeping of the process: from organizing, overseeing and compiling CRF workbooks, managing subject ID codes and other info to CRFs or ICFs, to maintenance of the post screening data archiving process relating to screening data, tests and measurement results. Ensure that the highest levels of ethical and medical confidentiality are maintained and that volunteer’s records are stored securely with restricted access.One of your main goals will be ensuring that our clinic screening capacities are used to its maximum potential, achieving the maximum number of participants for check-in as possible daily. Communication with participants will be the other key goal and you will co-ordinate the subjects callback process.
WHO YOU ARE
Prior comparable experience related to clinical trial participants recruitment is ideal, as well as exposure/familiarity with using CRFs, ICFs or Lab Sample management. However, we want to hear from you if you bring other experiences gained in a clinical setting (either at a Clinical Pharmacology Unit like ours, a CRO or a hospital environment).
University/college degree (life science, pharmacy or related subject). Able to demonstrate working knowledge of Microsoft Office (Outlook, Word, Excel)You will be responsible for a wide range of work assignments, so must be well organized, and able to liaise and manage the communication flow between multiple teams and several projects at the same time.
Fortrea is actively seeking motivated problem-solvers and creative thinkers who share our passion for overcoming barriers in clinical trials. Our unwavering commitment is to revolutionize the development process, ensuring the swift delivery of life-changing ideas and therapies to patients in need. Join our exceptional team and embrace a collaborative workspace where personal growth is nurtured, enabling you to make a meaningful global impact.
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Leeds, Leeds, United Kingdom LEE Fortrea Clinical Research Unit Limited Full timeAs a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access and technology solutions across more than 20 therapeutic areas. With over 19,000 staff...
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Leeds, United Kingdom Fortrea Full timeAs a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access and technology solutions across more than 20 therapeutic areas. With over 19,000 staff...
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