Do you want to be part of an organization that is making a difference in the lives of millions of people worldwide? If so, we want to hear from you!
Our Senior Specialist, Sample Report Management is a key contributor for the smooth operation of the Sample Management Team (SMT) within QPS's Translational Medicine (TLM) department. Sample Management ensures that client samples and other controlled materials are received, stored, distributed, tracked and returned safely, securely and without loss or damage. The process is regulated and vital to the success of clinical trials around the world.
This role requires attention to detail, organization, multi-tasking, and comfort interacting with people at all levels of the organization; we seek a team member who can share responsibilities and do what is needed in the moment - especially in a dynamic environment.
QPS' Story:
Since its inception, QPS has been assisting pharmaceutical, biotechnology and medical device companies with their drug development efforts by providing a full range of Neuropharmacology, DMPK, Toxicology, Bioanalysis, Translational Medicine, Early Phase Clinical and Phase II - IV Clinical Research services. To meet the needs of our clients, we strive to employ talented, caring and committed individuals who will work collaboratively towards achieving our mission of improving human health and the quality of life.
Team members enjoy challenging and rewarding work and are encouraged achieve their best. Underpinning the operation is a culture that values diversity, innovation, accountability, teamwork and a friendly atmosphere where performance is recognized and rewarded. We provide unique company benefits, training, and advancement opportunities. Most importantly, we value each of our team members as employees and as individuals.
If this sounds like your ideal work environment, then we would love to speak with you, so apply today! Please visit our website (www.qps.com) for more information and to see all current openings.
The Job
Work Location
Requirements
Combination of relevant education and experience that provides sufficient knowledge and skills to ensure incumbent's success in this role, such as:
University/college degree in a relevant scientific discipline and/or
Demonstrated experience in CRO, Clinical Research or another relevant field
Experience in an FDA-related or other regulated industry laboratory is preferred
Organized, with good detail-orientation
Proficient with MS Office, including Excel
Good interpersonal skills
Why You Should Apply
QPS, LLC is an Equal Employment Opportunity/Affirmative Action Employer. In accordance with federal, state, and local laws, we recruit, hire, promote and evaluate all personnel without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, citizenship status, physical disability, protected veteran status, or any other characteristic protected by law. Job applicants and present employees are evaluated solely on ability, experience, and the requirements of the job. In addition, QPS, LLC is a federal contractor and desires priority referrals of protected veterans.