Senior Scientist
2 months ago
Key Responsibilities:
- Could be assigned to assay development, qualification, validation and production expert in multiple assay types and mentor for more junior staff.
- Could have associate scientists and/or scientist I and II reporting to them
- Autonomous and proficient developing, planning, managing, conducting, reporting and troubleshooting multiple assay types to ensure scientific quality, regulatory expectations, and client satisfaction
- Assigned by management on studies and tasks based on scientific competency and training (can include method development, validation or sample analysis projects).
- For validations and sample analysis the Scientist can be assigned as Bioanalytical Principal Investigator and is the first point of contact for PM and/or clients for laboratory services and will manage and conduct method development, qualification , validation and production studies for clinical and non-clinical studies in compliance with the protocol/study plan, amendments, GCP, GLPs, SOPs and Best Practices;
- Manage project and order appropriate material, as needed
- When applicable, provide QC support on studies assigned to other team members in laboratory based on training and competencies
- When applicable, perform data batch review, perform multi-batch trend analysis, complete documentation as required by tracking deviations, events and reports of non-compliance and review or approved Memo to File or SOP/Protocol/Study Plan deviations;
- When applicable, provide a report and/or reporting of results, within study timelines and ensure any deviations/exception events are reflected as appropriate and assure that all analysis conducted is reported and is accurate;
- Manage as to maintain timeline and scheduling commitments
- When applicable review and provide comments and recommendations, as needed, for the bioanalytical portions of preclinical and clinical protocols, study plans, laboratory manuals, Data Transfer Agreements, and/or other document, as needed;
- Support and mentor Analysts in the daily operations for completion of sample analysis and/or validation studies and the analysts work;
- Support and mentor other team members based on expertise,
- Responsible for troubleshooting issues within the studies and be able to resolve them independently via development of appropriate procedure.
- Organize and communicate complex data sets in a clear and concise manner to key stakeholders from diverse backgrounds
- To write, review and updated method SOP as needed
- Participate in meetings with clients, conferences and scientific outreach
- Conduct applicable work in compliance with applicable SOPs, GCPs, GLPs, and observe all company guidelines and policies
- Ideally College degree and/or University degree in Chemistry, Biochemistry, Immunology or applicable field.
- Preferred experience in regulated clinical and/or preclinical studies with typically 3 years of experience.
- Minimal 2 years experience as Scientist II or equivalent.
- Knowledge of regulatory agency guidelines, must understand general SOPs and have excellent knowledge of GLP regulations.
- Good organizational skill, highly flexible, sense of urgency, excellent troubleshooting skills, client oriented, attentive to details
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