Job description
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 growing Clinical Research Services (CRS) department, has an immediate opening for a proven project management professional with pharmaceutical or CRO experience in the area of clinical research. In this role, you will be responsible for: coordinating and facilitating all project management activities; document management; managing study supplies; as well as quality control, finance and general responsibilities related to each assigned clinical research project.
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, team work 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
Project Management responsibilities to include working in close cooperation with the Project Manager and project team on all aspects of data entry, data flow, data transfer, data security, locking and quality and as well as data cleaning, while ensuring compliance with SOPs, pertinent industry standards, practices, guidelines, regulations and laws; and, evaluating all pertinent clinical data and information with the project team and overseeing the writing or revision of the annual, interim or final reports to the IRB
Documents management responsibilities to include anticipating document needs for each of the assigned Investigative Sites and ensuring adequate quantities are prepared for the timely initial distribution and subsequent re-supply of Investigative Sites throughout the duration of the clinical research project.
Quality Control management responsibilities to include ensuring the achievement and maintenance of compliance with all pertinent SOPs, industry standards, practices, guidelines, regulations and laws related to clinical research projects.
Financial management responsibilities to include Reconciling Investigator Sites’ and/or Vendor’s invoices Assisting the Project Manager in the Investigator and/or Vendor payment process
Requirements
- High School Diploma or equivalent, with some administrative experience in an environment requiring confidentiality and discretion
- Bachelor’s degree in related scientific discipline a plus
- 3 years pharmaceutical or CRO industrial experience in the area of clinical research
- Proficiency with MS Office products, including Outlook, Word, Excel and PowerPoint.
- Additional systems/programs/software includes: MS Project, CTMS, MS Access
Why You Should Apply
- Great learning opportunities, especially for those new to the field. Our seasoned professionals are here to support and work with you to explore your learning potential and career goals.
- Structured Career Ladders that provide excellent growth based on your personal aspirations.
- Bonuses and merit increases are a part of the QPS total rewards approach and are linked to individual, team and company performance.
- Solid Benefits package, including Company-matched 401(k), and Company-sponsored Group Life/AD&D and Short and Long-term Disability Insurance
- Park-like setting in Newark, Delaware
- Internal committees designed with the needs and enjoyment of QPS employees in mind.
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.
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