Job Description

Work Schedule

Standard (Mon-Fri)

Environmental Conditions

Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Office, Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.)

Job Description

Senior Study Lead

Department: Biopharmaceuticals

Location: Middleton, Wisconsin

This is a fully onsite role based at our GMP Laboratory in Middleton, WI. We welcome applicants from all locations within the US. Please note that relocation assistance is not provided for this position, and any relocation costs will be the responsibility of the candidate. Must be legally authorized to work in the United States without sponsorship. Must be able to pass a comprehensive background check, which includes a drug screening.

At Thermo Fisher Scientific, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our customers to make the world healthier, cleaner and safer. We provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through research, development and delivery of life-changing therapies. With clinical trials conducted in 100+ countries and ongoing development of novel frameworks for clinical research through our PPD clinical research portfolio, our work spans laboratory, digital and decentralized clinical trial services. Your determination to deliver quality and accuracy will improve health outcomes that people and communities depend on – now and in the future.

Our PPD® Laboratory Services team has a direct impact on improving patient health through the expertise of scientists, industry thought-leaders and therapeutic experts. As the world leader in serving science, our laboratory professionals bring their commitment to accuracy and quality to deliver groundbreaking innovations.

Role Overview

The Senior Study Lead is responsible for overseeing and managing multiple complex or large-scale routine projects (release, stability or quality control), ensuring seamless interaction with clients and internal leadership to communicate project updates, milestones, and strategic priorities. This role delivers high-quality outputs, conducts thorough reviews and evaluations of data, and prepares comprehensive protocols and reports.

The Senior Study Lead is accountable for managing quality records and ensuring strict adherence to regulatory guidelines and scientific standards for routine testing, including release, stability, and quality control projects. The Senior Study Lead holds decision-making authority for routine investigations, deviations, and risk-based assessments, ensuring scientifically sound and compliant outcomes. Leveraging extensive knowledge of laboratory systems, regulatory guidelines, and quality requirements, the Senior Study Lead provides expert oversight of routine testing, supports data trend evaluation, and proactively identifies risks or improvement opportunities. This role actively collaborates with cross-functional teams, including internal stakeholders, quality assurance, and SMEs, to align on project goals and drive successful outcomes.

The Senior Study Lead also mentors Study Lead team members and analysts, fosters audit readiness, and contributes to a culture of continuous improvement, scientific excellence, and ethical conduct. This role is accountable for driving routine study delivery, documentation, and client alignment, but may consult with Staff Scientist + for scientific conclusions on method-related decisions as well as overall study quality, client satisfaction, and successful delivery of complex or high-impact programs beyond individual project execution, and serves as a primary escalation point for complex technical and client-related issues associated with routine testing.

What you will do

• Independently draft and/or approve detailed and comprehensive technical documents, perform meticulous data/report reviews, and provide constructive feedback and guidance to Study Lead to ensure high-quality deliverables.
• Design and manage robust project study plans and complex program strategies, ensuring technical accuracy, high-quality outcomes, and alignment with client expectations and business objectives.
• Proactively identify solutions for technical challenges associated with routine testing, develop innovative and effective solutions, and mentor scientists in advanced problem-solving methods to enhance overall project outcomes.
• Identify and eliminate obstacles, develop strategic improvement plans, and continuously identify opportunities to optimize laboratory processes and project efficiency.
• Lead and oversee the execution and coordination of routine projects using established methods.
• Identify improvement opportunities and collaborate with internal stakeholders to evaluate and implement changes.
• Hold decision-making authority for routine investigations, deviations, and risk-based assessments, ensuring scientifically sound, compliant, and well-documented outcomes.
• Communicate complex technical information concisely and effectively with clients, lead technical visits and discussions, and prepare for audits or site visits to ensure compliance and client satisfaction.
• Lead audit readiness efforts by ensuring studies, documentation, and processes are inspection-ready; serve as a key contact during audits and drive resolution of audit observations, including CAPAs and systemic improvements.
• Review and/or approve client deliverable documents including routine protocols, reports, and quality records to ensure quality and compliance.
• Develop and evaluate technical Key Performance Indicators (KPIs), collaborate closely with clients and internal stakeholders to drive continuous improvement, and ensure alignment with project goals and regulatory standards.
• Support comprehensive contract reviews, evaluate scientific proposals with a critical eye, provide well-informed recommendations, and accurately estimate resource needs to support project planning and execution.
• Train and mentor Study Lead and other staff on compliance, audit readiness, and unbiased problem-solving techniques, promote ethical behavior and integrity, and actively support continuous improvement initiatives to foster a culture of excellence.
• Accountable for overall study quality, data integrity, and compliance across assigned programs, ensuring alignment with GMP, regulatory requirements, and internal standards.

Key Requirements

Education and Experience

• Bachelor's degree or equivalent and relevant formal academic / vocational qualification.
• Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to 8+ years experience) or equivalent combination of education, training, and experience.

In some cases, an equivalency, consisting of a combination of appropriate education, training and/or directly related experience, will be considered sufficient for an individual to meet the requirements of the role.

Knowledge, Skills, and Abilities:

• Advanced knowledge of routine analytical testing, instrumentation, and laboratory systems, with the ability to troubleshoot established methods.
• Strong understanding and application of regulatory requirements (e.g., GMP, FDA guidelines), with the ability to advise on compliance and risk mitigation strategies.
• Expertise in data evaluation, including trend analysis, outlier detection, and interpretation of complex data sets to support scientific and operational decisions.
• Demonstrated leadership in managing multiple complex or large-scale routine projects, balancing priorities, resolving conflicts, and meeting challenging deadlines.
• Highly proficient in Microsoft Office applications (Word, Excel, PowerPoint, Teams, SharePoint), with functional skills in Power BI for data visualization and reporting.
• Skilled in the use of laboratory information management systems (LIMS) and data collection software relevant to analytical testing environments.
• Excellent written and verbal communication skills, with the ability to draft high-quality technical documents and clearly communicate complex scientific information to clients and internal stakeholders.
• Strong technical writing skills, including authorship and/or review of protocols, reports, and quality records.
• Ability to conduct root cause analyses, lead investigations, and develop effective corrective and preventive action plans.
• Demonstrated capability to train, mentor, and coach junior staff and Study Lead team members, fostering problem-solving, audit readiness, and compliance awareness.
• Proven ability to identify and implement process improvements, drive innovation, and support continuous improvement initiatives across routine testing operations.
• Strong attention to detail, data integrity, and documentation practices in compliance with internal SOPs and external regulatory standards.
• Ability to build and maintain positive relationships with internal teams and clients, manage expectations, and influence project outcomes through collaboration and trust.
• Demonstrated ability to give and receive constructive feedback in a professional and solutions-oriented manner.
• High level of integrity and confidentiality, with a consistent focus on ethical behavior, scientific rigor, and quality.

Work Environment

Thermo Fisher Scientific values the health and wellbeing of our employees. We support and encourage individuals to create a healthy and balanced environment where they can thrive. Below is listed the working environment/requirements for this role:

• Able to communicate, receive, and understand information and ideas with diverse groups of people in a comprehensible and reasonable manner.
• Able to work upright and stationary and/or standing for typical working hours.
• Able to lift and move objects up to 25 pounds.
• Able to work in non-traditional work environments.
• Able to use and learn standard office equipment and technology with proficiency.
• May have exposure to potentially hazardous elements, including infectious agents, typically found in healthcare or laboratory environments.
• Able to perform successfully under pressure while prioritizing and handling multiple projects or activities.

Our Mission is to enable our customers to make the world healthier, cleaner and safer. Watch as our colleagues explain 5 reasons to work with us. As one team of 100,000+ colleagues, we share a common set of values - Integrity, Intensity, Innovation and Involvement - working together to accelerate research, solve complex scientific challenges, drive technological innovation and support patients in need. #StartYourStory with PPD, part of Thermo Fisher Scientific, where diverse experiences, backgrounds and perspectives are valued.

Apply today! http://jobs.thermofisher.com

Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.

Accessibility/Disability Access

Job Seekers with a Disability: Thermo Fisher Scientific offers accessibility service for job seekers requiring accommodations in the job application process. For example, this may include individuals requiring assistance because of hearing, vision, mobility, or cognitive impairments. If you are a job seeker with a disability, or assisting a person with a disability, and require accessibility assistance or an accommodation to apply for one of our jobs, please submit a request by telephone at 1-855-471-2255*. Please include your contact information and specific details about your required accommodation to support you during the job application process.

*This telephone line is reserved solely for job seekers with disabilities requiring accessibility assistance or an accommodation in the job application process. Messages left for other purposes, such as not being able to get into the career website, following up on an application, or other non-disability related technical issues will not receive a response.