What are the responsibilities and job description for the Quality Control Specialist position at QPS Holdings, LLC?
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 Stage Clinical and Phase I IV Clinical Research services. We welcome individuals who want to be part of our growing organization. QPS is an innovative, dynamic organization that strives to employ talented, caring and committed employees who will work collaboratively towards achieving our mission of improving human health and the quality of life. QPS offers challenging and rewarding work in its four core business areas and support functions. Underpinning the operation is a culture that values diversity, innovation and accountability. Employees are encouraged to take responsibility and achieve their best, both as individuals and as team members.
Description
A Quality Control Specialist (QC) is an entry-level position responsible for the maintenance of clinical trial eSource Documentation. This position is responsible for auditing eSource to ensure accuracy, timely reporting to Data Entry to keep on track with contact timelines, Standard Operating Procedures (SOPs), study protocols and Good Clinical Practice (GCP) guidelines.
Responsibilities
QPS is an equal opportunity employer. In accordance with anti-discrimination law, it is the purpose of this policy to effectuate these principles and mandates. QPS prohibits discrimination and harassment of any type and affords equal employment opportunities to employees and applicants without regard to race, color, religion, sex, sexual orientation, gender identity or expression, pregnancy, age, national origin, disability status, genetic information, protected veteran status, or any other characteristic protected by law. QPS conforms to the spirit as well as to the letter of all applicable laws and regulations.
Description
A Quality Control Specialist (QC) is an entry-level position responsible for the maintenance of clinical trial eSource Documentation. This position is responsible for auditing eSource to ensure accuracy, timely reporting to Data Entry to keep on track with contact timelines, Standard Operating Procedures (SOPs), study protocols and Good Clinical Practice (GCP) guidelines.
Responsibilities
- Develop a full understanding of SOPs, study protocols, and lab manuals for multiple clinical trials.
- Effectively organize study information for efficient recall of documentation needed.
- Perform departmental task to remain in compliance with SOPs, study protocols, and lab manuals.
- Audit 100% of eSource documentation to analyze, identify, query and resolve data issues/inconsistencies based on SOPs, study protocols and lab manuals.
- Provide customer service, which includes effective communication with other staff and clients.
- Assist with training new or less-experienced data entry staff on study-specific procedures and data entry guidelines.
- Other duties as assigned.
- Combination of relevant education & experience that provides sufficient knowledge & skills to ensure incumbent’s success in this role, such as:
- High school diploma or equivalent required.
- Previous experience with data entry, data management, or Microsoft Office applications preferred (minimum of 6 months).
- Strong time management and organizational skills with attention to detail.
- Effective written and verbal communication skills.
- Ability to work both independently and collaboratively in a team environment.
- Demonstrated ability to follow through on tasks and consistently meet expectations.
- Job duties may include additional responsibilities as needed and are subject to change.
QPS is an equal opportunity employer. In accordance with anti-discrimination law, it is the purpose of this policy to effectuate these principles and mandates. QPS prohibits discrimination and harassment of any type and affords equal employment opportunities to employees and applicants without regard to race, color, religion, sex, sexual orientation, gender identity or expression, pregnancy, age, national origin, disability status, genetic information, protected veteran status, or any other characteristic protected by law. QPS conforms to the spirit as well as to the letter of all applicable laws and regulations.