- Ensure the confidentiality of clinical trial participants and sponsors is respected.
- Maintain and advocate a high level of quality and customer service within the department.
- Record, track and ensure the resolution of data queries.
- May assist in sponsor/regulatory audits.
- May document and/or report clinical trial related deviations (i.e. SOP, protocol).
- Understand protocol driven timed study events and acceptable collection windows (protocol and/or SOP driven) for the timed events.
- Proactively communicate issues and/or problem resolutions to departmental supervisors and managers.
- Complete and/or maintain training as required per jobs needs.
- Perform general administrative tasks when required.
- High School Diploma or GED required; college degree and related work experience preferred.
- Good Communication
- Detail oriented
- Well organized
- Customer service focused
- Able to work in fast-paced environment
- Health/Dental/Vision Insurance Plans
- 401(k)/RRSP with Employer Match
- Paid Vacation and Holidays
- Paid Sick and Bereavement Leave
- Employee Assistance & Telehealth Programs
- Training & Development Programs
- Employee Referral Bonus Program
- Job Family OS-2
- Pay Type Hourly
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Clinical Quality Control Associate I - Overland Park, United States - Altasciences
Description
Your New CompanyAt Altasciences we allmove in unison to assist and work in the discovery, development, and manufacturing of new drug therapies to get them faster to people who need them. No matter your role, we all play an important part and you will have a significant impact on the health and well-being of people across the globe. By living our values of Employee Development, Customer Focus, Quality and Excellence, Respect and Integrity, we look to foster a passionate and collaborative work environment and we are looking for talented and enthusiastic people, like you, to join our growing team Whether you're a recent college graduate or seeking your next career opportunity, it's time to discover your future at Altasciences. We are better together and together We Are Altasciences.
About The Role
The Clinical Quality Control Associate I is responsible for the quality control (QC) review of clinical trial data and assisting the Quality Systems team with QC related tasks. The Clinical Quality Control Associate I will conduct tasks performed within compliance of study protocol, Good Clinical Practices (GCP) and Standard Operating Procedures (SOPs).
What You'll Do Here
Benefits
Altasciences offers a wide variety of benefits to help our employees live healthy and fulfilling lives both at and outside of work.
Altasciences' Benefits Package Includes:
MOVING IN UNISON TO DELIVER A BIG IMPACT WITH A PERSONAL TOUCH
Altasciences is an equal opportunity employer committed to diversity and inclusion. Our goal is to attract, develop and retain highly talented employees from diverse backgrounds, allowing us to benefit from a wide variety of experiences and perspectives. All qualified applicants will receive consideration for employment without regard to age, race, color, religion, creed, sex, sexual orientation, gender identity, national origin, disability or any other protected grounds under applicable legislation. Reasonable accommodations for persons with disabilities during the recruitment process are available upon request. Altasciences warrants adherence to applicable labor laws, including non-use of forced, prison or child labor, in violation of US and Canada laws, in its operations or supply chain.
Join us at Altasciences
Other details
