Clinical Trial Participant Recruitment Coordinator
4 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 USand 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 Coordinator.
- You will need to be able to commit to working 5 out of 7 days per week and to be open to shift work, including twilight, nights and weekends.
- This is a _zero-hours, Bank Contract position _offering _flexible working hours_._
- This means you will have the _potential to work up to 37 hours per week. However, _you may not be guaranteed these hours every week as these _will vary depending on business needs._
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, and
- 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.
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
- Conduct daily QC of screening Case Report Forms (CRF).
- Ensure that the highest levels of ethical and medical confidentiality are maintained and that volunteer’s records are stored securely with restricted access.
WHO YOU ARE
Prior comparable experience related to clinical trial participants recruitment is ideal, as well as exposure/familiarity wit 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).
- 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 proud to be an Equal Opportunity Employer:
As an EOE/AA employer, Fortrea strives for diversity and inclusion in the workforce and does not tolerate harassment or discrimination of any kind. We make employment decisions based on the needs of our business and the qualifications of the individual and do not discriminate based upon race, religion, color, national origin, gender (including pregnancy or other medical conditions/needs), family or parental status, marital, civil union or domestic partnership status, sexual orientation, gender identity, gender expression, personal appearance, age, veteran status, disability, genetic information, or any other legally protected characteristic. We encourage all to apply.
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