Laboratory Sample Coordinator, Leeds
Leeds | www.pharmiweb.jobs |
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 early-stage Clinical Research Organizations in the world, operating four ultramodern Clinical Research Units in the UK and US, the jewel of 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 Early Clinical research (and 7 minutes walking from the train station!)
And this is where you come in because the laboratory in the Clinic is expanding and now seeking our next Laboratory Sample Coordinator.
• This is an office-based, full-time and permanent jobs, working hours are 37 hours per week, five days over seven.
• You will be required to work a mix of shifts, including weekend, twilight and night (compensated with flexi time or overtime pay.)
WHO YOU ARE
• You have professional experience in sample management within a laboratory setting or familiarity with basic laboratory techniques, procedures, equipment and instrumentation.
• Educated to GCSE standard or equivalent.
Nice to have:
• Exposure to ICH-GCP, cGMP and/or GLP settings.
We need someone who thrives and is familiar working in an environment that is:
• Fast paced: where no deviations from the study protocol are allowed, and meeting deadlines is crucial.
• Changing priorities constantly demanding quick adaptation and prioritization skills.
• Attention to detail focused, emphasizing accuracy in data analysis
• Team-oriented culture where collaboration and communication are key.
• Technology-driven, with data management done directly into electronic systems.
ON A NORMAL DAY, YOU WILL...
Learn. And grow. No two days will be the same because you will be exposed to a wide variety of Therapeutic Indications and study types (from single and multiple ascending dose, first-in-human, to food effect, drug to drug interactions, etc.)
The core of your work will be supporting international Phase 1 clinical trials. All our teams in Drapers Yard live to answer one question: “ is the drug safe? ” Under this framework, you will:
• Coordinate the storage and shipment of samples according to study protocol and Lab Manual requirements.
• Dispatch samples to external laboratories globally.
• Ensure adherence to correct shipping procedures in compliance with international regulations for biohazardous and dangerous goods.
Our expectations are significant: from managing a wide variety of study design and protocol specifications concurrently, to calibrating Lab equipment, monitoring temperature, and navigating global custom requirements, you will oversee the shipment of thousands of samples daily.
... and the rewards too: This team is gaining increasing relevance across the organization. You will participate in international projects among our clinics to globally align sample coordination enhancing efficiencies. There is genuine potential for grow over time into team leadership or training roles.
DISCOVER THE FORTREA CAREER ADVANTAGE
You will have the clinical trial participants next door! Under the same roof, we have: a 100 beds clinic, a cutting-edge cGMP pharmacy and a state-of-the-art Lab.
Witness firsthand clinical research unfolding in real time. When the drug you worked with gets approved, you know you´ll touch many patient´s lives around the world.
Join us in fulfilling our mission to enable life-changing healthcare solutions. Apply now and embark on a extraordinary scientific journey with Fortrea.
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. For more information about Fortrea, visit www.fortrea.com.
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.
For more information about how we collect and store your personal data, please see our Privacy Statement.
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 early-stage Clinical Research Organizations in the world, operating four ultramodern Clinical Research Units in the UK and US, the jewel of 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 Early Clinical research (and 7 minutes walking from the train station!)
And this is where you come in because the laboratory in the Clinic is expanding and now seeking our next Laboratory Sample Coordinator.
• This is an office-based, full-time and permanent jobs, working hours are 37 hours per week, five days over seven.
• You will be required to work a mix of shifts, including weekend, twilight and night (compensated with flexi time or overtime pay.)
WHO YOU ARE
• You have professional experience in sample management within a laboratory setting or familiarity with basic laboratory techniques, procedures, equipment and instrumentation.
• Educated to GCSE standard or equivalent.
Nice to have:
• Exposure to ICH-GCP, cGMP and/or GLP settings.
We need someone who thrives and is familiar working in an environment that is:
• Fast paced: where no deviations from the study protocol are allowed, and meeting deadlines is crucial.
• Changing priorities constantly demanding quick adaptation and prioritization skills.
• Attention to detail focused, emphasizing accuracy in data analysis
• Team-oriented culture where collaboration and communication are key.
• Technology-driven, with data management done directly into electronic systems.
ON A NORMAL DAY, YOU WILL...
Learn. And grow. No two days will be the same because you will be exposed to a wide variety of Therapeutic Indications and study types (from single and multiple ascending dose, first-in-human, to food effect, drug to drug interactions, etc.)
The core of your work will be supporting international Phase 1 clinical trials. All our teams in Drapers Yard live to answer one question: “ is the drug safe? ” Under this framework, you will:
• Coordinate the storage and shipment of samples according to study protocol and Lab Manual requirements.
• Dispatch samples to external laboratories globally.
• Ensure adherence to correct shipping procedures in compliance with international regulations for biohazardous and dangerous goods.
Our expectations are significant: from managing a wide variety of study design and protocol specifications concurrently, to calibrating Lab equipment, monitoring temperature, and navigating global custom requirements, you will oversee the shipment of thousands of samples daily.
... and the rewards too: This team is gaining increasing relevance across the organization. You will participate in international projects among our clinics to globally align sample coordination enhancing efficiencies. There is genuine potential for grow over time into team leadership or training roles.
DISCOVER THE FORTREA CAREER ADVANTAGE
You will have the clinical trial participants next door! Under the same roof, we have: a 100 beds clinic, a cutting-edge cGMP pharmacy and a state-of-the-art Lab.
Witness firsthand clinical research unfolding in real time. When the drug you worked with gets approved, you know you´ll touch many patient´s lives around the world.
Join us in fulfilling our mission to enable life-changing healthcare solutions. Apply now and embark on a extraordinary scientific journey with Fortrea.
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. For more information about Fortrea, visit www.fortrea.com.
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.
For more information about how we collect and store your personal data, please see our Privacy Statement.
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