Lead LCMS Scientist – Preclinical Method Development

Altasciences; Columbia Township, Northern (MO, KY); Hybrid; USD 90,000 - 130,000; Full time

Benefits offered by this job

Health/Dental/Vision Insurance Plans

401(k)/RRSP with Employer Match

Paid Vacation and Holidays

Paid Sick and Bereavement Leave

Employee Assistance & Telehealth

Training & Development Programs

Employee Referral Bonus Program

Job summary

Altasciences Preclinical Columbia is seeking a scientific leader to join our team on the frontlines of discovery. Lead method development, validate LC-MS/MS assays, and contribute to preclinical and clinical study support.

You will supervise lab staff, ensure GLP compliance, collaborate with clients, manage timelines, and stay current with innovative methodologies in a collaborative, patient-focused environment.

Qualifications

• Advanced degree in chemistry, biology, or pharmaceutical science with hands-on lab experience.
• Willingness to step into leadership roles; prior supervising is a plus.
• Proficient with LIMS and electronic notebooks; strong data management skills.
• Excellent written and verbal communications; able to engage with clients.

Responsibilities

• Develop and validate LC-MS/MS assays for preclinical and clinical studies.
• Analyze study samples with precision to support toxicology endpoints.
• Ensure GLP compliance and meticulous documentation.
• Manage project timelines and coordinate with stakeholders.
• Collaborate with clients to design studies and assays.
• Contribute to method validation and qualification efforts.
• Provide supervision to laboratory staff.

Skills

Supervisory skills

Communication

Project management

Analytical thinking

Education

Bachelor's/Master's/PhD in chemistry, biology or pharmaceutical science

Tools

LIMS

Electronic notebooks

Job description

Altasciences Preclinical Columbia is seeking a scientific leader to join our team on the frontlines of discovery. Lead method development, validate LC-MS/MS assays, and contribute to preclinical and clinical study support.

You will supervise lab staff, ensure GLP compliance, collaborate with clients, manage timelines, and stay current with innovative methodologies in a collaborative, patient-focused environment.