Laboratory Specialist II
Altasciences
Summary
The Laboratory Specialist II is responsible for the processing and assisting with the management of biological samples collected during clinical trials. The Laboratory Specialist II will ensure tasks performed are conducted within compliance of study protocol, Good Clinical Practices (GCP) and Standard Operating Procedures (SOPs).
Job description
About The Role
The Laboratory Specialist II is responsible for the processing and assisting with the management of biological samples collected during clinical trials. The Laboratory Specialist II will ensure tasks performed are conducted within compliance of study protocol, Good Clinical Practices (GCP) and Standard Operating Procedures (SOPs).
What You'll Do Here
- Ensure the confidentiality of clinical trial participants and sponsors is respected, while maintaining a high level of quality within the department.
- Report procedural deviations, issues and/or problem resolutions to appropriate supervisory team members.
- Understand protocol driven timed study events, which may include but are not limited to, centrifugation, study and clinical diagnostic sample handling/processing, storing samples and acceptable windows (protocol and/or SOP driven) for the timed events.
- Coordinate with external vendors (i.e. shipment couriers, central lab).
- Act as a mentor to the Laboratory Specialist I team members.
- Assist with maintaining equipment used in sample management (i.e. freezers, refrigerators, centrifuges) and document accordingly.
- Assist in the resolution of data queries.
- Other tasks assigned by management.
What You'll Need to Succeed
- High School Diploma or GED required; college degree and related work experience preferred
- Minimum of 3-6 years of related experience
- Ability to read and interpret technical documents and industry specific manuals.
- Ability to write advanced reports and correspondence.
- Ability to speak effectively before groups of customers or employees of the organization.
- Excellent verbal and written communication skills.
- Well developed interpersonal skills are required.
- Personal/professional integrity and proven discretion in handling confidential information.
- Ability to develop strong trusting relationships in order to gain support and achieve results.
- Capable of managing multiple conflicting priorities.
- Must be self-directed, motivated, and have a willingness to take the initiative to identify and anticipate study needs and make recommendations for implementation to management.
- Detail oriented, well organized, customer service focused and ability to work in fast-paced environment.
Holiday/Weekend/Evening Work Hours: Ability to work overtime, holidays, weekends, and evening hours as needed
Requirements
- High School Diploma or GED required
- College degree and related work experience preferred
- Minimum of 3-6 years of related experience
- Ability to read and interpret technical documents and industry specific manuals
- Ability to write advanced reports and correspondence
- Ability to speak effectively before groups of customers or employees
- Excellent verbal and written communication skills
- Well developed interpersonal skills
- Personal/professional integrity and proven discretion in handling confidential information
- Ability to develop strong trusting relationships
- Capable of managing multiple conflicting priorities
- Self-directed, motivated, and willing to take initiative
- Detail oriented, well organized, customer service focused
- Ability to work in fast-paced environment
- Ability to work overtime, holidays, weekends, and evening hours as needed
- Must be legally authorized to work in the United States
Benefits
- Health Insurance
- Dental Insurance
- Vision Insurance
- 401(k) Matching
- RRSP Matching
- Paid Vacation
- Paid Holidays
- Paid Sick Leave
- Bereavement Leave
- Employee Assistance Program
- Telehealth Programs
- Training & Development
- Employee Referral Bonus
Company overview
Altasciences is a forward-thinking, mid-size contract research organization (CRO) and contract development manufacturing organization (CDMO) that provides integrated, full-service solutions for early phase drug development. Founded in 1992 and owned by Novo Holdings A/S, the company offers pharmaceutical and biotechnology companies a proven, flexible approach to preclinical and clinical pharmacology studies. Their comprehensive services include preclinical safety testing, clinical pharmacology and proof of concept studies, bioanalysis, formulation development, manufacturing and analytical services, program management, medical writing, biostatistics, and data management. With over 1,800 employees across eight facilities in the U.S. and Canada, Altasciences has established itself as a trusted partner for drug development from lead candidate selection through clinical proof of concept and beyond. The company's integrated CRO/CDMO model enables seamless transitions between development phases, reducing complexities, mitigating risks, and accelerating timelines for clients ranging from startups to global pharmaceutical leaders.