The Senior Scientist ensures study design; execution and reporting align with regulatory and client project specifications. The Senior Scientist provides critical client consultation throughout study life cycle and ensures lab compliance to study design. This role will support Electrophysiology projects including cardiac safety screening in a GLP-compliant electrophysiology lab and serve as a Principal Investigator for regulated studies. This role requires technical expertise portfolio leadership leadership competencies and proficiency in client communication within a contract research organization.
Senior Scientist Regulatory Cardiac Safety / Electrophysiology (Scientist II) responsibilities include but are not limited to the following :
The Senior Scientist is a scientific leadership position responsible for providing guidance and alignment between our customer base the industry at large commercial teams and service operations. This role is a hands-on laboratory-based role and will be collaborative and influential in a broad network of business functions in support of delivering high quality services to our valued customers and driving business growth brand recognition and alignment with Eurofins core competencies. This position will train and mentor junior staff responsible to take informed decision to move projects ahead set direction champion change and directly contribute to achieving departments goals and strategies.
- Develops client and stakeholder relationships through technical leadership and collaboration
- Manages client projects in all phases of study life cycle from study design to reporting
- Provides guidance and oversight for compliance and scientific integrity of the studies to ensure that studies are performed in a compliant manner
- Understands and follows all procedures and processes required for work performed under Regulatory Compliance (i.e. GxP FDA / GLP and GCP OECD CLIA etc.) and completes annual GLP training
- Directs investigations of service operations such as deviation reports non-conforming reports corrective action reports etc. Produces documentation according to established standards
- Drafts and approves operations documents to assure consistency with regulatory standards and requirements. (I.e. SOPs batch records training records etc.)
- Responsible for data generation review analysis review and ensuring accuracy and integrity of reporting
- Provides scientific guidance that supports technical writing and final review of Validation Plans and Reports as required
- Supports client services team in generating proposals RFPs study plans and scope of work preparation. Assists pricing team in completing custom pricing and cost analysis
- Completes required training and supports 100% of Employee Health and Safety requirements
- Manages responsible use of confidential IT and business systems as required
- Ensures accurate data management and reporting with the highest integrity and manages quality control on project data and reports
- Accountable for delivering to unit and site key performance metrics (quality delivery on time)
- Supports site goals and demonstrates Eurofins competencies as defined in the job plan
- Provides training to colleagues and external end users when required
- Performs other duties as assigned
Qualifications :
Basic Minimum Education Qualifications :
M.A. or M.S. with minimum 5 years relevant experience
OR
Ph.D. with minimum 3 years relevant experience
Basic Minimum Qualifications :
Demonstrated experience in manual patch clamp electrophysiology in a GLP-compliant laboratory is a plus.Scientific expertise in Ion Channel electrophysiology and applications to execute safety pre-clinical studies.Technical experience and knowledge in supporting compound cardiac safety profiling within drug discovery programs from early drug discovery to IND submission life cycle.Experience developing client relationships supporting technical correspondence drafting and presenting scientific proposals to clients.Experience in drafting and executing equipment and method validation according to 21CFR11 compliance.Authorization to work in the United States indefinitely without restriction or sponsorship.The Ideal Candidate Possesses the Following :
Demonstrates a positive attitude capacity for team environment and exhibits a genuine interest in drug discovery in support of advancing human health.Excellent interpersonal verbal and written skills including ability to prepare detailed scientific reports and group presentations.Demonstrates a working understanding of international regulatory requirements and aptitude to stay relevant on topical scientific publications.Ability to support project management plan and coordinate multiple projects simultaneously with appropriate allocation of available resources.Demonstrated experience in working effectively with lab operations business development marketing and outsourcing stakeholders.Experience with leading and influencing cross-functional teams effectivelyAdditional Information :
Position is full-time with overtime as needed. Candidates currently living within a commutable distance of St. Charles MO are encouraged to apply.
Excellent full time benefits including comprehensive medical coverage dental and vision optionsLife and disability insurance401(k) with company matchPaid vacation and holidaysEurofins USA Discovery Services is a Disabled and Veteran Equal Employment Opportunity employer.
Remote Work : No
Employment Type : Full-time
Key Skills
Laboratory Experience,Mammalian Cell Culture,Biochemistry,Assays,Protein Purification,Research Experience,Next Generation Sequencing,Research & Development,cGMP,Cell Culture,Molecular Biology,Flow Cytometry
Experience : years
Vacancy : 1