Job Details
Operational Data Steward Lexington, MA
Must be able to work on a W2
Bioanalytical Data reviewer/ Quality Control - Contractor
This position is responsible for the quality control of all nonGLP data generated in the Nonclinical Pharmacology group.
Key Responsibilities:
Work closely with scientists within the ADME group to verify bioanalytical data generated using HPLC-FD and LC-MS/MS.
Work closely with scientists within the in-vivo pharmacology group to verify in-vivo and Pharmacodynamic (qPCR) data.
Review and verify all data to ensure accuracy, completeness, and compliance with internal guidelines and acceptance criteria.
Generate reports/checklist for all QC findings, along with subsequent discussions with relevant scientists in order to resolve issues.
Interpret data and provide insight for in-vivo studies, ensuring alignment with study objectives and protocols.
Collaborate with cross-functional teams to support raw data verification.
Ensure data integrity and quality by adhering to internal and other regulatory guidelines. .
Enhance QC initiatives through the identification and implementation of best practices in data review and analysis.
Qualifications:
Strong analytical skills with a keen eye for detail.
Familiarity with analytical software s.
Familiarity with regulatory guidelines and standards related to bioanalytical data review.
Excellent communication and collaboration skills.
Experience:
Prior experience in quality control of Scientific data.
Minimum of 1 year experience with data review/QC, preferred 3-5 years of experience.
Education:
A degree in a relevant scientific discipline, such as Biochemistry, Biotechnology, Pharmacology, or related fields
Term & Start
- 12-month contract
- FT, M-F 40hr/week
- Pay Rate: $32/HR ($64K Annually)
- Onsite in Lexington, MA Hybrid 3 days a week