Clinical Project Associate Jobs in Three Rivers, MI

An Associate Director within the Molecular Biology discipline is responsible for providing general oversight and management of staff that execute in vitro, molecular and/or cell-based assays supporting Discovery through Clinical work. This individual is expected to provide leadership and guidance for staff development; verify staff compliance with regulatory and other requirements; develop efficient and scientifically valid processes and procedures; provide budget oversight, and contribute to quality metrics, performance metrics, and project risk assessments. They will demonstrate effective communication with both on-site and off-site peers as well as with Sponsors. They may function as a Principal Investigator, Individual Scientist and/or Project Scientist if required. They may manage cross discipline interdependencies in collaboration with leadership as well as provide mentorship. 

• Efficiently perform supervisory responsibilities in accordance with organizational policies and applicable laws to include interviewing, hiring, training and developing employees
• Effectively demonstrates the behaviors and performance characteristics as described in the CRL DNA
• Develop organizational strength by hiring, identifying and developing personnel who are scientifically and/or technically strong
• Establishes a positive culture and atmosphere to maintain good retention and low turnover using available tools and metrics (e.g. Glint survey results)
• Provides effective short- and long-term solutions that support continuous improvement
• Maintain critical thinking, troubleshooting and time management skills aligned with needs of operational areas
• Consistently demonstrates role model leadership and effective communication skills through informal discussions with peers, supervisor, team, cross-site, and externally with collaborators and sponsors
• Ensure laboratory tasks and operations are executed in compliance with SOPs, protocols, regulatory requirements as needed
• Accurately review and approve Standard Operating Procedures (SOPs), protocols, policies, best practices and study procedures
• Maintain contemporaneous knowledge of regulatory requirements
• Effectively plans, assigns and directs work within one operational area with expanded scope and/or complexity
• Establishes and actively monitors performance metrics for operational area
• Demonstrates consistent enforcement of policies with employees and manages performance based on the requirements of the employee’s role.  Effectively applies progressive discipline as required
• Actively communicates and effectively collaborates and builds strong working relationships with multiple departments within site
• Effectively assists in providing accurate costing estimates for components of applicable studies
• Skillfully oversees the design, conduct, interpretation and reporting of studies as required by operational area
• Effectively utilizes project management systems
• Effectively leads implementation of new procedures and refinement of existing procedures to meet current and future business needs
• Effectively aligns operational resources with the current needs in one operational area
• Actively manages cross-service line interdependencies in collaboration with organizational leadership
• Effectively leads planning (resource management, budgets and study coordination) as well as track budgets and spend vs. revenue for one operational area
• Actively collaborates and consults with prospective Sponsors, providing scientific expertise and developing ongoing Sponsor relationships
• Provides effective leadership, expert consultation and mentorship to cross-functional company teams

• Bachelor’s degree in a scientific field
• CRO experience preferred
• 11-14 years of relevant experience
• 5 years of management experience required
• Experience with Immuno Toxicology Assays, Molecular Biology & Flow Cytometry is required

 Other: 

• Ability to communicate verbally and in writing at all levels inside and outside the organization
• Basic familiarity with Microsoft Office Suite
• Computer skills, commensurate with Essential Functions, including the ability to learn a validated system
• Ability to work extended hours beyond normal work schedule to include, but not limited to evenings, weekends, extended shifts, and/or extra shifts, sometimes on short notice
• Ability to work under specific time constraints
   

Workplace Requirements:

• While performing the duties of this job, the employee must be able to perform general office and/or laboratory procedures, which require, talking, hearing, standing, or sitting for long periods of time, typing/entering data into a computer, using appropriate instruments, reaching with hands and arms, and wearing safety equipment (PPE) according to OSHA regulations and company standards.
• Specific vision abilities required by this job include close vision, color vision, depth perception, and the ability to adjust focus.
• General office working conditions, the noise level in the work environment is usually quiet.While performing the duties of this job the employee may occasionally be required to wear protective clothing (goggles, face shield, surgical mask, cap, gloves, scrubs, boots), work near toxic or caustic chemicals, work with biohazards, and/or work with live animals with risk of exposure to allergens and/or zoonotic diseases.
• The employee may occasionally be exposed to fumes or airborne particles, unpleasant odors, and/or wet, humid and/or extreme temperature conditions.
• All employees are required to satisfactorily perform the essential duties and responsibilities of their position.
• The essential duties and responsibilities listed above are not intended to be construed as an exhaustive list of all responsibilities, duties and skills required. Duties and responsibilities may change without notice.
• Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions of this job or as otherwise required to comply with applicable law.  

Must be authorized to work in the United States without a sponsor visa.

This position is 100% on site.

The pay range for this position is $140-150k/year. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location.