Scientific Coordinator - Bioanalytical Chemistry
Listed on 2026-07-04
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Research/Development
Clinical Research, Research Scientist, Medical Technologist & Lab Technician -
Healthcare
Clinical Research, Medical Technologist & Lab Technician
Provide protocol and direct support to Research Scientist and Sponsors with all aspects of data management. Assist with management of QA audit and assure necessary corrections and follow-up take place.
ESSENTIAL DUTIES AND RESPONSIBILITIES- Interact regularly with Research Scientists and Sponsors: respond to sponsor‑requests for information.
- Assure a full understanding of assigned projects and results, including objectives, timelines and reporting requirements.
- For clinical studies: maintain master inventory list.
- Document and communicate discrepancies to Sponsor and resolve as appropriate.
- Work with Sponsors, Data Managers and Research Scientist to coordinate data transfer agreements.
- Create data transfer files and provide to Sponsor and Data Managers. Reconcile discrepancies as needed.
- Tabulate study data and generate report tables.
- Extract information from study data to generate results and conclusions in conjunction with the Research Scientist.
- Under direction of the Research Scientist, receive, review and QC reports and make recommended corrections as appropriate.
- Assemble data package and ensure data is GLP compliant prior to QA submission.
- Assist with QA audits and assure necessary corrections and follow‑up take place.
- Support in documentation of deviations and help in drafting new SOPs. Assist in the maintenance and communication of departmental systems and SOPs.
- Perform all other related duties as assigned.
- Education:
Bachelor's degree (B.A./B.S.) or equivalent in science or related discipline. - Experience:
2-4 years related experience in a laboratory or scientific research environment. Requires analytical thinking skills and a good understanding of scientific processes. - Certification/Licensure:
None. - Other:
Knowledge of Good Laboratory Practice (GLP) regulations. Familiar with scientific protocols and reports and all components required for completeness. Computer skills including MS Office software and database management. Strong organizational skills and attention to detail.
The pay range for this position is $29.00/hour. Salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location.
BENEFITSBenefit offerings may include bonus/incentives based on performance, 401K, paid time off, stock purchase program, Health and wellness coverage, employee and family wellbeing support programs, and work‑life balance flexibility.
EQUAL EMPLOYMENT OPPORTUNITYCharles River is an equal opportunity employer and is committed to providing equal employment opportunities for all qualified applicants and employees without regard to race, color, sex, religion, national origin, ancestry, age, mental or physical disability, family status, pregnancy, military or veteran status, or any other characteristic protected by federal, state, or local laws.
It is unlawful in some states (including Massachusetts) to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.
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