ZipRecruiter

Log In

1

Edc Project Manager Jobs in Minnesota (NOW HIRING)

Mobia Medical, Inc.

Clinical Study Manager

Fridley, MN · On-site

$110K - $160K/yr

Experience with EDC systems, CTMS platforms, and clinical trial tracking tools You'll thrive in this role if you are: * Highly organized with strong project management and prioritization skills * A ...

EarthDaily Analytics

Director, Product Management

Osseo, MN · On-site

$165K - $205K/yr

The EDC will be the most powerful global change detection and change monitoring system ever ... project managers and finance, HR, and IT professionals. Our Agro Product Management & Customer ...

Apply Early

Lancesoft

Sr Clinical Research Spec

MN · On-site +1

$50 - $55/hr

Advanced knowledge of clinical trial management systems (CTMS), electronic data capture (EDC), and ... Responsible for entire projects or processes, contributing to work group objectives. * Innovation ...

All JobsEdc Project JobsEdc Project Manager JobsEdc Project Manager Jobs in Minnesota

Edc Project Manager information

Is EDC a good place to work?

An EDC Project Manager typically works in a structured environment that values project management skills, certifications like PMP, and effective communication. The work often involves coordinating teams, managing budgets, and adhering to deadlines, which can provide valuable experience in the field. Overall, the work environment depends on the specific organization and its culture, but project management roles generally offer opportunities for professional growth.

Can I make 100k as a project manager?

Edc Project Managers with significant experience, certifications like PMP, and working in high-demand industries can earn salaries of $100,000 or more annually. Salary levels depend on factors such as location, company size, and project complexity, with senior or specialized project managers more likely to reach or exceed this threshold.

What projects do EDC employees work on?

EDC Project Managers oversee a variety of projects related to economic development, infrastructure, and community improvement initiatives. They coordinate with stakeholders, manage project timelines, budgets, and ensure successful implementation using project management tools and methodologies.

What are some common challenges faced by EDC Project Managers when implementing new electronic data capture systems?

EDC Project Managers often encounter challenges such as ensuring seamless integration of the new system with existing clinical trial workflows, managing diverse stakeholder expectations, and maintaining data quality throughout the study. They must also handle tight timelines and adapt quickly to regulatory changes or sponsor requirements. Effective communication with both technical teams and clinical staff is crucial to overcoming these obstacles and ensuring successful project delivery.

What are the key skills and qualifications needed to thrive as an EDC Project Manager, and why are they important?

To thrive as an EDC Project Manager, you need expertise in clinical data management, project coordination, and a solid understanding of Electronic Data Capture (EDC) systems, usually supported by a degree in life sciences or related fields. Familiarity with EDC platforms like Medidata Rave or Oracle InForm, along with certifications such as PMP or CDISC, is highly valuable. Strong organizational, problem-solving, and communication skills help you effectively lead cross-functional teams and manage client expectations. These competencies ensure successful EDC project delivery, regulatory compliance, and high-quality clinical trial data.

What are EDC Project Managers?

EDC Project Managers are professionals who oversee the planning, execution, and monitoring of projects related to Electronic Data Capture (EDC) systems, primarily within clinical research and pharmaceutical industries. They coordinate between cross-functional teams, manage timelines, ensure regulatory compliance, and address any issues that arise during the data collection process. Their goal is to ensure that EDC systems are implemented efficiently and effectively, supporting the overall success of clinical trials. EDC Project Managers also act as the main point of contact for sponsors and stakeholders, ensuring that project objectives and quality standards are met.

What is the highest paying project manager?

The highest paying project managers are often those in industries like oil and gas, IT, or construction, with salaries exceeding $150,000 annually. Senior project managers with PMP certification and extensive experience in complex projects tend to earn the most, especially in large organizations or specialized sectors.

What is the difference between Edc Project Manager vs Electrical Project Manager?

AspectEdc Project ManagerElectrical Project Manager
CertificationsPMP, OSHA, EDC-specific trainingPMP, OSHA, Electrical licenses
Work EnvironmentEnergy, utility, and infrastructure projectsConstruction, industrial, and commercial electrical projects
Industry UsageCommon in energy distribution and utility sectorsCommon in construction and industrial sectors
Job FocusDistribution systems, substations, and energy deliveryBuilding wiring, electrical systems, and installations

The Edc Project Manager primarily oversees energy distribution and utility infrastructure projects, focusing on energy delivery systems. In contrast, the Electrical Project Manager handles a broader range of electrical construction projects, including commercial and industrial wiring. Both roles require similar certifications but differ in industry focus and project types.

What are popular job titles related to Edc Project Manager jobs in Minnesota? For Edc Project Manager jobs in Minnesota, the most frequently searched job titles are:
What job categories do people searching Edc Project Manager jobs in Minnesota look for? The top searched job categories for Edc Project Manager jobs in Minnesota are:
What cities in Minnesota are hiring for Edc Project Manager jobs? Cities in Minnesota with the most Edc Project Manager job openings:
Edc Project Manager jobs near you

Clinical Study Manager

Mobia Medical, Inc.

Fridley, MN • On-site

$110K - $160K/yr

Full-time

Medical, Dental, Vision, Retirement, PTO

Posted 17 days ago

Job description

About Mobia Medical
Mobia Medical is a commercial-stage medtech company delivering breakthrough stroke recovery solutions. The company's Vivistim® Paired VNS™ Therapy is the first and only FDA-approved implantable solution designed to improve function in chronic ischemic stroke survivors with moderate to severe upper limb impairments. Vivistim® Paired VNS™ Therapy combines targeted vagus nerve stimulation with functional movement to promote neuroplasticity and improve the brain's ability to relearn motor skills. Mobia Medical is mobilizing patients, providers, and care partners to establish a better way forward in stroke care.
About the role
The Clinical Study Manager is a key member of the Clinical Affairs team, responsible for leading the operational execution and management of clinical studies that support the company's clinical development programs.
In this role, you will partner closely with Clinical, Regulatory, Data Management, Biostatistics, and cross-functional teams to ensure clinical studies are executed efficiently, compliantly, and with high-quality data outcomes. You will play a critical role in supporting feasibility, pivotal, and post-market studies while driving operational excellence and maintaining strong relationships with investigational sites and external partners.
What you'll do
Lead clinical study execution and operations
  • Manage clinical studies from start-up through close-out, ensuring timelines, deliverables, and study objectives are achieved
  • Develop and manage study timelines, enrollment plans, tracking tools, and operational deliverables
  • Support implementation of monitoring plans, enrollment initiatives, and risk mitigation strategies
  • Identify and proactively resolve operational, enrollment, compliance, and data quality challenges

Drive site management and investigator engagement
  • Support site qualification, initiation, interim monitoring, and close-out activities
  • Build and maintain strong relationships with investigators, research coordinators, and study personnel
  • Coordinate investigator meetings and site training activities
  • Ensure investigators and site staff are trained on protocols, investigational devices, EDC systems, and regulatory requirements
  • Support enrollment and retention initiatives while ensuring protocol adherence and informed consent compliance

Ensure data quality and regulatory compliance
  • Ensure accurate, complete, and timely collection of clinical trial data
  • Monitor study metrics and trends to identify risks or quality concerns
  • Identify protocol deviations, safety concerns, and noncompliance issues and ensure appropriate escalation and resolution
  • Support audit and inspection readiness activities
  • Assist with preparation of study reports, annual reports, and clinical documentation submissions

Collaborate cross-functionally and support continuous improvement
  • Partner with Data Management, Biostatistics, Regulatory, and Clinical teams to support study execution and reporting
  • Manage and oversee CROs, vendors, and external study partners to ensure high-quality deliverables
  • Contribute to process improvement initiatives within Clinical Operations

Qualifications
What you bring:
  • Bachelor's degree in life sciences, nursing, engineering, or related scientific discipline required
  • Advanced degree preferred
  • 5+ years of clinical research experience in medical device, biotechnology, or pharmaceutical industries
  • 3+ years of clinical study management or clinical operations experience
  • Experience supporting feasibility, pivotal, and/or post-market clinical studies
  • Strong understanding of clinical trial operations, site management, and study execution

Preferred qualifications:
  • Experience supporting multicenter clinical trials
  • Experience managing CROs and external vendors
  • Strong knowledge of FDA regulations, GCP, and clinical research compliance requirements
  • Experience with EDC systems, CTMS platforms, and clinical trial tracking tools

You'll thrive in this role if you are:
  • Highly organized with strong project management and prioritization skills
  • A collaborative team player who works effectively across cross-functional groups
  • A proactive problem solver who can identify and mitigate study risks
  • Detail-oriented with a strong commitment to data quality and regulatory compliance
  • An effective communicator who builds trusted relationships with study sites and internal stakeholders

Equal Opportunity Employer
Mobia Medical provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state or local laws.
Benefits
Mobia Medical provides a comprehensive benefits program to employees. It includes medical, dental and vision plans along with an FSA. Employees may participate in the company 401(k) plan with company matching. The company offers an unlimited Paid Time Off (PTO) program and approximately 18 paid company holidays per year.
Apply now
The pay range for this role is:
110,000 - 160,000 USD per year (US National)

Apply