Quality Control Data Reviewer - BioPharma Services USA

Company: Think Research
Location: Saint Louis
Posted on: June 24, 2022

Job Description:

Job Description .
The Company
BioPharma Services Inc. is a subsidiary of Think Research.
BioPharma Services was founded by two surgeons dedicated to advancing medical science to improve the life and spirit of their patients. With this same dedication and vision in mind, these physicians brought life to BioPharma.
Through each success, and even some failures, the perpetual drive to make BioPharma great has been determined by the will and dedication of our people. The will to empower their colleagues, friends and teammates to excel in all facets of clinical research and inspire performance to achieve greatness.
It is with this same culture and brand of excellence that we welcome our clients. To experience the team community that has propelled us into a global leader in medical research, to be a client-focused partner, where people and patients matter.
Again, we invite you to come and meet our people. Our people who have learned that success is better achieved and celebrated as a team than as an individual.
Why Us?
It's not every day that you have the chance to change the way your friends and family are cared for - Make an impact!
Everything we do - and we do it with passion - is to improve the quality of life for patients who benefit from the clinical trials that we perform for global pharmaceutical companies.
We're growing, and so will you with leaders who will support your development through mentorship and other opportunities
Collaborative, creative, dynamic and flexible work environment, with a start-up spirit
The Role
Responsible for reviewing of all study related documentation to ensure the quality, reliability, accuracy, completeness and consistency according to Protocol, SOPs and Regulatory requirements. Other responsibilities as assigned.
You Will Have The Opportunity To:
Review study files after completion and ensure that they are accurate and legible according to protocol, SOPs and regulations
Ensure all prepared study source documents and/or forms are in accordance to protocols, SOPs and regulations
Review all other study related documentation: medical screening files, pharmacy labels and files, final report tabulations and PK STAT input and output as assigned
Observe, on a random basis, clinical procedures during the conduct of studies, sample bundling and shipping process
Provide reports of the reviewed data to relevant personnel/department
Perform other duties as assigned by supervisor
What You Will Bring:
Post-secondary degree in a science or healthcare related discipline, or equivalent work experience.
1-2 years of relevant clinical research experience, knowledge of ICH-GCPs and professional experience working in CRO
Ability to accommodate a flexible work schedule and to adapt to changing priorities; able to work under pressure.
Excellent communication skills
Excellent computer skills
Certification in Clinical Research is an asset.
Think Research and all subsidiaries are proud to be an equal opportunity employer and is committed to creating a diverse and inclusive workplace, free of discrimination and harassment.
We provide equal employment opportunities (EEO) to all employees and applicants regardless of race, colour, religion, gender, gender identity or expression, sexual orientation, national origin, genetics, disability, age, or veteran status.
We are committed to providing accommodations for people with disabilities. Should you require an accommodation, we would like to work with you to meet your needs.
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Keywords: Think Research, St. Louis , Quality Control Data Reviewer - BioPharma Services USA, Other , Saint Louis, Missouri