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Manager Medtech Jobs in Washington (NOW HIRING)

IQVIA

MedTech Site Manager 1

Washington, DC · On-site

$74K - $124K/yr

Position Overview The In-House Clinical Research Associate/MedTech Site Manager 1 will be a critical team member reporting directly to the Director of Clinical Affairs, to support clinical trial ...

IQVIA

MedTech Site Manager 1

Washington, DC

$74K - $124K/yr

Position Overview The In-House Clinical Research Associate/MedTech Site Manager 1 will be a critical team member reporting directly to the Director of Clinical Affairs, to support clinical trial ...

Jj

Capital Key Account manager - East

Washington, DC · On-site +1

MedTech Sales Job Sub Function: Capital Sales -- MedTech (Commission) Job Category: Professional All Job Posting Locations: Baltimore, Maryland, United States, Delaware (Any City), Maryland (Any City ...

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Manager Medtech information

What does a manager Medtech do?

A Manager in Medtech oversees teams and projects within the medical technology industry, ensuring the development, production, and delivery of medical devices or health-related technologies. Their responsibilities often include coordinating cross-functional teams, managing budgets, ensuring regulatory compliance, and driving product innovation. They play a crucial role in aligning business objectives with technological advancements to improve patient outcomes. Additionally, they may interact with stakeholders, healthcare professionals, and regulatory bodies to ensure products meet market and safety standards.

What are the key skills and qualifications needed to thrive as a manager Medtech?

To excel as a Manager Medtech, you need a solid background in medical technology, regulatory compliance, and team leadership, often supported by a degree in biomedical engineering or a related field. Familiarity with quality management systems (such as ISO 13485), medical device regulations (FDA, CE), and project management tools is essential. Strong interpersonal, problem-solving, and strategic planning skills help you guide teams and communicate effectively with stakeholders. These abilities are crucial to ensure product safety, regulatory adherence, and successful project delivery in the competitive medtech industry.

How does a manager Medtech typically collaborate with cross-functional teams to drive successful product development?

A Manager Medtech frequently works alongside R&D, regulatory affairs, marketing, and quality assurance teams to ensure that new medical technologies are developed efficiently and in compliance with industry standards. This role acts as a bridge between technical teams and business stakeholders, coordinating timelines, addressing technical and regulatory challenges, and aligning product features with market needs. Effective communication and strong organizational skills are essential, as the manager must facilitate regular meetings, resolve conflicts, and keep projects on track to meet both innovation and compliance goals.

MedTech Site Manager 1

Washington, DC • On-site

IQVIA
Health Care and Social Assistance • 10K+ employees
Learn more about IQVIAexternal

$74K - $124K/yr

Full-time

Posted 29 days ago

IQVIA rating

8.1

Company rating: 8.1 out of 10

Based on 53 frontline employees who took The Breakroom Quiz

Job description

MCRA is part of IQVIA MedTech. As a trusted CRO and advisory partner, IQVIA MedTech and MCRA deliver integrated lifecycle solutions for the medical device and diagnostics industry. Together, we support innovation from concept to commercialization, offering expertise in regulatory strategy, clinical trial design and execution, market access, and post-market optimization. Our teams combine deep therapeutic knowledge with advanced data and technology to help clients make smarter decisions and thrive in the market. Join our team to help shape the future of MedTech.Position OverviewThe In-House Clinical Research Associate/MedTech Site Manager 1 will be a critical team member reporting directly to the Director of Clinical Affairs, to support clinical trial operations for the firm's clientele. Responsible for management of investigator site and Clinical Research Associate (CRA) activities for assigned studies. The In-House CRA will execute Clinical Affairs functions in accordance with Good Clinical Practice (GCP) guidelines, Standard Operating Procedures (SOPs), and any other applicable regulatory requirements.Position Responsibilities
  • Review and approve research and study regulatory documents required for the implementation, monitoring, and evaluation of clinical trials.
  • Review clinical protocols to ensure collection of data needed for regulatory submissions
  • Contribute to protocol-specific manuals, plans, and documents as needed.
  • Ensure that monitoring activities (remote and on-site) are completed in accordance with company/client SOPs and Clinical Monitoring Plan.
  • Assist project manager with clinical study planning and management, as required.
  • Develop and maintain positive relationships both internal and external to project, including clients, team members, and site personnel (PIs, Study coordinators, etc.).
  • Assist in the identification and recruitment of potential investigators and study sites, as needed.
  • Ensure Trial Master File is accurate and complete throughout the lifecycle of the project.
  • Assist with site training for assigned clinical trials.
  • Assist with site audits and site quality management activities as needed.
  • Maintain current knowledge of GCP and FDA guidance as it relates to clinical research, as well as current clinical related developments in the assigned therapeutic areas.
Required Qualifications
  • Bachelor's degree (B.A./B.S.) in pharmacy, pharmaceutics or a related scientific discipline
  • 2+ years of clinical trial experience. Monitoring experience preferred.
  • Comprehensive knowledge/ fluency of GCPs and clinical monitoring procedures
  • Understanding of therapeutic area for assigned clinical projects.
  • Experience using Electronic Data Capture (EDC) and clinical trial management systems.
  • Possesses strong written and verbal communication and presentation skills.
  • Strong research, analytical, critical-thinking and problem solving skills
  • PC/Technical skills - MS Office, Excel, Word, PowerPoint (Endnote experience is a plus)

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more athttps://jobs.iqvia.com

IQVIA is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other status protected by applicable law. https://jobs.iqvia.com/eoe

IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

The potential base pay range for this role, when annualized, is $74,500.00 - $124,100.00. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.

What IQVIA employees say

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About IQVIA

Sourced by ZipRecruiter

At IQVIA, we are passionate about helping customers and partners improve results and patient outcomes. Everything we do contributes to this vision for creating a healthier world. In today’s healthcare environment, it’s not only about how much data, information, and technology you have at your fingertips – it’s what you do with it. IQVIA is focused on making intelligent connections for customers across the entire healthcare ecosystem to help you drive healthcare forward. Whether that means partnering with novel technology companies to boost patient engagement, leveraging AI & machine learning to accelerate results, or using decentralized trials to reach the right patients wherever they are – we are always looking for smarter ways to move you forward.

Industry

Health care and social assistance

Company size

10,000+ Employees

Headquarters location

Durham, NC, US

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