As a leading contract research organization (CRO), Labcorp Drug Development provides comprehensive drug development solutions for a range of industries. Our services cover the preclinical, clinical and post-market phases of drug development, the product life cycles for medical device and diagnostics and development services paired with regulatory support for the chemical testing and crop protection industries.
Labcorp Drug Development is a global leader in nonclinical safety assessment, clinical trial testing and clinical trial management services. Our unique perspectives are based on decades of scientific, medical and regulatory expertise.
Typical day to day Coordinator tasks include:
Prepare, update, record, collate, distribute, archive and dispose of documents (electronic and physical files)
Be responsible for document processing to electronic Trial Master File (eTMF)
Be involved in validation activities
Distribute and track safety reports (SUSARs)
Be responsible for site invoice requests and invoice processing
We offer you:
work as part of a diverse and stable team
in-depth Onboarding, including personal support from your mentor
flexible working hours, capped overtime and compensatory time off in lieu
a permanent employment contract
travel time = work time
highly competitive compensation packages including Christmas and vacation allowances
regular, merit-based salary adjustments
significant employer contributions to an attractive pension scheme
excellent training and career development opportunities
strong support from Line Management and more than 20'000 colleagues worldwide
the world's most renowned pharmaceutical companies as our satisfied, repeat customers for many years
degree in a relevant field such as life sciences, (veterinary) medicine, pharmacology, biology, chemistry, health care, health management, nursing etc.
in lieu of the above, a completed vocational education or professional experience (e. G. As study nurse, study coordinator) in a relevant field
first professional experience in clinical research / drug development
basic understanding of biology and biological processes
familiarity with and/or practical application of ICH guidelines and GCP
proficient user of IT applications such as MS Office and possibly even clinical software - e. G. Study databases, eTMF (Veeva Vault)
solid organizational and project management skills with a keen attention to detail and a high sense of accountability
excellent communication skills in business fluent German and English - verbal and written - and strong interpersonal skills are a must
Did you know?
In July 2022, Labcorp announced its intention to spin off its clinical development business as a separate public company, subject to the satisfaction of certain customary conditions. Fortrea will become the new brand identity for our Clinical Development business in connection with the spin-off, which is expected in mid-2023.
We believe that the exceptional is possible when you have the right partner, so we are looking for the right people to help build a transformative force in Clinical Development. www. Fortrea. Com
Labcorp is proud to be an Equal Opportunity Employer:
As an EOE/AA employer, Labcorp 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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