NORTHERN BIOMEDICAL RESEARCH INC dbaNorthernB logo

Research Supervisor

NORTHERN BIOMEDICAL RESEARCH INC dbaNorthernB

Norton Shores, MIOnsitePosted 33 days ago
Full TimeMid LevelResearch & ScientistCRO
Original posting ↗

Summary

Supervisors are responsible for the direct oversight and development of their team while maintaining day-to-day operations for their department. They actively support tasks as needed and oversee scheduling and cross-functional collaboration to ensure efficient workflow. They implement policies, processes, and procedures that affect staff and operations, while clearly communicating expectations, aligning team activities with business objectives and driving continuous improvement.

Job description

Role Summary

Supervisors are responsible for the direct oversight and development of their team while maintaining day-to-day operations for their department. They actively support tasks as needed and oversee scheduling and cross-functional collaboration to ensure efficient workflow. They implement policies, processes, and procedures that affect staff and operations, while clearly communicating expectations, aligning team activities with business objectives and driving continuous improvement.

Role Responsibilities

  • Provide quality oversight of study conduct through scheduling, planning, training, data review, archival, and general project management.
  • Ensure that all direct reports adhere to standard operating procedures (SOPs), protocols, and applicable regulatory guidelines, assuming full responsibility for their compliance.
  • Identify and provide the resources necessary for staff to complete functions.
  • Serve as the liaison between staff, other departments/groups, and management to communicate expectations and business needs.
  • Oversee performance, development, training needs, and accomplishments for all direct reports.
  • Assure timely and compliant performance of required equipment maintenance activities.
  • Develop and maintain Standard Operating Procedures (SOPs).
  • Communicate expectations, departmental policies, procedures, and business needs to direct reports.
  • Track departmental metrics.
  • Recognize, initiate, and lead process improvement activities.
  • Coordinate the support of outside contractors or vendors.
  • Perform routine and complex technical procedures and functions as needed.
  • Other duties as assigned.

Role Requirements

  • Bachelor’s degree in Life Sciences or a related discipline preferred.
  • An equivalent combination of education, experience, and/or leadership role experience may be accepted as a satisfactory substitute for the specific education and experience listed above.
  • Minimum of 3 years of relevant lab experience required.
  • Minimum of 1 year of management experience is preferred.
  • Proficiency with Microsoft Office applications and ability to learn and use additional applications.
  • Excellent written and oral communication skills.
  • Excellent understanding of study design and protocols.
  • Advanced understanding of laboratory operations, federal regulations, and data handling in a GLP environment.
  • Ability to resolve complex issues.

Behavioral Expectations

  • Time Management
  • Conflict Resolution
  • Decision Making
  • Team Player
  • Adaptable
  • Ability to Multi-Task and Work in a Fast-Paced Environment

Special Requirements

The role will spend approximately 75% in an office setting and 25% in the laboratory. There will be exposure to human and animal potentially infectious materials and chemicals. Ability to don and wear personal protective gear for extended periods of time, including N95 masks and respirators. Physical Requirements: Ability to lift and carry up to 50lbs. Flexibility to work beyond typical work schedule including, but not limited to, evenings, weekends, and extended shifts with short notice on an as-needed basis.

Requirements

  • Bachelor’s degree in Life Sciences or a related discipline preferred
  • Minimum of 3 years of relevant lab experience required
  • Minimum of 1 year of management experience is preferred
  • Proficiency with Microsoft Office applications
  • Excellent written and oral communication skills
  • Excellent understanding of study design and protocols
  • Advanced understanding of laboratory operations, federal regulations, and data handling in a GLP environment
  • Ability to resolve complex issues

Company overview

Northern Biomedical Research Inc, operating as Northern Bio, is a preclinical contract research organization (CRO) specializing in non-GLP and GLP-compliant research services for pharmaceutical and biotechnology companies. Founded in 1993 and headquartered in Michigan with three research facilities across the state, the company focuses on targeted drug delivery, molecular biology, and bioanalysis to support drug development. Northern Bio offers expertise across multiple therapeutic areas including neuroscience, ophthalmology, cardiovascular diseases, metabolic disorders, rare diseases, and surgical models. The company employs advanced surgical techniques and research methodologies to maximize therapeutic impact and facilitate regulatory approval. With a team of 201-500 experienced scientists, operational leaders, and veterinary staff, Northern Bio emphasizes animal welfare through adherence to the 3Rs principles (replacement, reduction, refinement). The organization maintains GLP compliance (21 CFR Part 58) and electronic records compliance (21 CFR Part 11) through its independent quality assurance unit. Northern Bio serves as a collaborative partner to sponsors, providing customized preclinical study solutions and expert guidance throughout the drug development process.

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