Clinical Research Manager - CRM

Medtronic; Minneapolis (MN); Remote; USD 129,000 - 195,000; Full time

Job summary

A leading company in healthcare technology is seeking a Clinical Research Manager to oversee clinical studies and manage a team. This remote role involves ensuring compliance with regulatory requirements, leading studies, and developing strategies for product approvals. Candidates should possess a Bachelor’s degree and significant clinical research experience.

Benefits

Competitive salary

Flexible benefits

Additional perks

Qualifications

• At least 5 years of Clinical Research experience or an advanced degree with 3 years of experience.
• Strong leadership and teamwork skills.

Responsibilities

• Oversee all clinical activities related to clinical studies.
• Develop and implement regulatory strategies for product approvals.
• Manage clinical programs and budgets.

Skills

Leadership skills

Global teamwork experience

Knowledge of GCPs

Regulatory guidelines

Clinical trial management

Education

Bachelor’s degree

Advanced degree (Masters, PhD, MD)

Job description

Join to apply for the Clinical Research Manager - CRM role at Medtronic

We anticipate the application window for this opening will close on - 28 May 2025.

At Medtronic, you can begin a lifelong career of exploration and innovation, helping to champion healthcare access and equity for all. You’ll lead with purpose, breaking down barriers to innovation in a more connected, compassionate world.

A Day in the Life

Location: Remote position within the United States

Travel: up to 25% (domestic and may include international travel).

In this role as a Clinical Research Manager (CRM), you will oversee all clinical activities related to one or more clinical studies, managing daily in-house activities. This is a people leadership role. The CRM reports to the US Sr. Clinical Research Director and manages a team of Clinical Research Specialists at various levels.

Responsibilities may include:

• Leading clinical studies and regulatory affairs related to product approval, ensuring studies are scientifically valid, meet regulatory requirements, and are conducted ethically.
• Developing and implementing regulatory strategies for timely product approvals worldwide.
• Ensuring regulatory submissions are accurate and compliant.
• Representing Medtronic in the country/region, building relationships with internal and external stakeholders.
• Leading execution of local and global studies across multiple therapies.

Additional responsibilities:

• Managing clinical programs, preparing study documentation, supervising investigator training, and overseeing study accuracy.
• Developing and managing budgets.
• Overseeing resources and priorities, supervising staff, and interfacing with regulatory agencies.
• Performing supervisory duties and collaborating with field staff and other departments.
• Overseeing activities of CROs and supporting post-clinical activities and market launches.

Must Have (Minimum Requirements):

• Bachelor’s degree.
• At least 5 years of Clinical Research experience or an advanced degree with 3 years of experience.

Nice to Have (Preferred Qualifications):

• Advanced degree (Masters, PhD, MD).
• Leadership skills, global teamwork experience, and prior experience in medical device clinical trials.
• Knowledge of GCPs, regulatory guidelines, and clinical trial management.

Physical Job Requirements

Employees must meet physical demands to perform essential functions, with accommodations available for disabilities.

Benefits & Compensation

Competitive salary, flexible benefits, and additional perks. Salary range: $129,600 - $194,400 annually.

About Medtronic

Medtronic is a leader in healthcare technology, committed to innovation and diversity, with a mission to improve lives globally.