Sr. Clinical Operations Manager

16 Minutes ago • 10 Years + • $129,375 PA - $207,000 PA
Operations

Job Description

The Senior Clinical Operations Manager leads the coordination and execution of clinical studies, ensuring strict compliance with regulatory requirements (ISO, GCP, FDA) and Philips procedures. This role involves managing complex negotiations, providing updates to senior management, and driving continuous improvement in clinical trial processes while maintaining alignment with Philips standards and timelines. The manager also serves as a subject matter expert for study sites and investigators, reviews documentation, and develops study plans.
Good To Have:
  • Knowledge and experience with peripheral vascular.
Must Have:
  • Lead and oversee all aspects of clinical study management, ensuring strict compliance with regulatory requirements (ISO, GCP, FDA) and Philips procedures.
  • Serve as a subject matter expert and primary resource for study sites and investigators.
  • Review and verify study documentation, data, and deliverables for accuracy, completeness, and regulatory compliance.
  • Develop study plans and protocols, manage cross-functional relationships, and facilitate communication.
  • Monitor study progress, conduct data analysis, manage risks, and deliver timely updates and recommendations to senior management.
  • 10+ years of experience in clinical research with some experience leading medical device clinical trials.
  • Knowledge and experience with cardiac or coronary is required.
  • Strong knowledge of all relevant regulations, standards, and guidelines (ISO, GCP, etc.).
  • Familiarity with Cath Lab Operations is required.
  • Bachelor’s degree or higher in a related field, or nursing background with extensive clinical research experience in the cardiac space.
  • Expert level independent contributor able to multi-task and prioritize, taking a proactive approach to drive efficiency.
  • Willing and able to travel up to 25%.
Perks:
  • Generous PTO
  • 401k (up to 7% match)
  • HSA (with company contribution)
  • Stock purchase plan
  • Education reimbursement

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Job Title

Sr. Clinical Operations Manager

Job Description

Senior Clinical Operations Manager (Plymouth, MN local)

The Senior Clinical Operations Manager leads the coordination and execution of clinical studies, collaborating with stakeholders to optimize operations and ensure regulatory compliance. This role manages complex negotiations, provides updates to senior management, and drives continuous improvement in clinical trial processes while maintaining alignment with Philips standards and timelines.

Your role:

  • Leads and oversees all aspects of clinical study management, ensuring strict compliance with regulatory requirements (ISO, GCP, FDA) and Philips procedures, including site assessments, monitoring, training, and data integrity.
  • Serves as a subject matter expert and primary resource for study sites and investigators, providing guidance on protocol, regulatory standards, and best practices for clinical research involving medical devices.
  • Reviews and verifies study documentation, data, and deliverables for accuracy, completeness, and regulatory compliance, proactively addressing issues and discrepancies to maintain study quality.
  • Develops study plans and protocols, manages cross-functional relationships, and facilitates communication among internal departments and external collaborators to achieve project objectives and optimize study processes.
  • Monitors study progress, conducts data analysis, manages risks, and delivers timely updates and recommendations to senior management, ensuring alignment with budgets, schedules, and continuous improvement goals.

You're the right fit if:

  • You’ve acquired 10+ years of experience in clinical research with some experience leading medical device clinical trials. Knowledge and experience with peripheral vascular strongly preferred; cardiac or coronary experience and knowledge required.
  • Your skills include strong knowledge of all relevant regulations, standards, and guidelines (ISO, GCP, etc.). Familiarity with Cath Lab Operations is required.
  • You have a bachelor’s degree or higher in a related field. Will also consider nursing backgrounds with extensive clinical research experience in the cardiac space.
  • You must be able to successfully perform the following minimum Physical, Cognitive and Environmental job requirements with or without accommodation for this position.
  • You’re an expert level independent contributor who is able to multi-task a prioritize based on business needs, and take a proactive approach to drive efficiency in clinical research operations. You are willing and able to travel up to 25% as required by business needs.

How we work together

We believe that we are better together than apart. For our office-based teams, this means working in-person at least 3 days per week. Onsite roles require full-time presence in the company’s facilities. Field roles are most effectively done outside of the company’s main facilities, generally at the customers’ or suppliers’ locations.

This is a field-based role with a preference to hire someone local to Plymouth, MN who can be onsite 2 days per week.

Philips Transparency Details

The pay range for this position in Minnesota is $129,375 to $207,000.

The actual base pay offered may vary within the posted ranges depending on multiple factors including job-related knowledge/skills, experience, business needs, geographical location, and internal equity.

In addition, other compensation, such as an annual incentive bonus, sales commission or long-term incentives may be offered. Employees are eligible to participate in our comprehensive Philips Total Rewards benefits program, which includes a generous PTO, 401k (up to 7% match), HSA (with company contribution), stock purchase plan, education reimbursement and much more. Details about our benefits can be found here.

At Philips, it is not typical for an individual to be hired at or near the top end of the range for their role and compensation decisions are dependent upon the facts and circumstances of each case.

Additional Information

US work authorization is a precondition of employment. The company will not consider candidates who require sponsorship for a work-authorized visa, now or in the future.

Company relocation benefits will not be provided for this position. For this position, you must reside in or within commuting distance to Plymouth, MN**.

#LI-PH1

This requisition is expected to stay active for 45 days but may close earlier if a successful candidate is selected or business necessity dictates. Interested candidates are encouraged to apply as soon as possible to ensure consideration.

Philips is an Equal Employment and Opportunity Employer including Disability/Vets and maintains a drug-free workplace.

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