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Remote Medical Device Project Manager Jobs in Ladera Ranch, CA

Diality

Clinical Research Associate

Irvine, CA · Remote

$120K - $135K/yr

This position plays a key role in supporting research projects at Diality, combing responsibilities ... device-specific regulatory pathways. * Experience with managing remote monitoring activities or ...

Glaukos

Cornea Regional Business Manager

San Clemente, CA · Remote

$270K/yr

Minimum 3 years of ophthalmic medical device, surgical device, or pharmaceutical sales experience ... Total Targeted Compensation $270K+ Plus RSU's. #GKOSUS #LI-remote Generous. Innovative. Leadership ...

Glaukos

Cornea Regional Business Manager

San Clemente, CA · Remote

$270K/yr

Minimum 3 years of ophthalmic medical device, surgical device, or pharmaceutical sales experience ... Total Targeted Compensation $270K+ Plus RSU's. #GKOSUS #LI-remote Generous. Innovative. Leadership ...

Socotec

Project Environmental Professional

Irvine, CA · On-site +1

$130K - $150K/yr

Manage project schedules, budgets, deliverables, and client expectations. * Serve as a primary ... day remote/ hybrid schedule SOCOTEC is an Equal Opportunity Employer. SOCOTEC is an Equal ...

esVolta

Project Engineer

Newport Beach, CA · Remote

Our diverse management team has many decades of experience in the renewable energy, utility, and ... Medical, dental and vision care benefits * Monthly cell phone stipend This position is classified ...

esVolta LP

Project Engineer

Newport Beach, CA · On-site

Our diverse management team has many decades of experience in the renewable energy, utility, and ... Medical, dental and vision care benefits * Monthly cell phone stipend This position is classified ...

PM2CM

Cost Engineer Hybrid-Remote

Anaheim, CA · On-site +1

PM2CM, Inc., (Project Management to Construction Management) is a professional services company ... Hybrid-Remote (Tuesday and Wednesday in the office/field) JOB OPPORTUNITY: WE ARE HIRING JUNIOR ...

Argus Medical Management

Patient Care Coordinator

Anaheim, CA · Remote

$18.25 - $24/hr

Provide Remote Patient Monitoring (RPM) and Chronic Care Management (CCM) services to patients ... device logistics, and scheduling initial setup calls. * Provide technical support for our medical ...

IQVIA

Clinical Trial Psych Rater

Carlsbad, CA · Remote

Remote/Virtual Hours: Estimated 10-16 hours per month Role: Clinical Specialist About IQVIA IQVIA ... We partner with the world's leading pharmaceutical, biotechnology, and medical device companies to ...

IQVIA

Clinical Trial Psych Rater

Carlsbad, CA · Remote

Remote/Virtual Hours: Estimated 10-16 hours per month Role: Clinical Specialist About IQVIA IQVIA ... We partner with the world's leading pharmaceutical, biotechnology, and medical device companies to ...

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All JobsMedical Device Project JobsRemote Medical Device Project Manager JobsRemote Medical Device Project Manager Jobs in Ladera Ranch, CA

Remote Medical Device Project Manager information

See Ladera Ranch, CA salary details

$40.9K

$109.2K

$172.2K

How much do remote medical device project manager jobs pay per year?

As of Sep 2, 2026, the average yearly pay for remote medical device project manager in Ladera Ranch, CA is $109,154.00, according to ZipRecruiter salary data. Most workers in this role earn between $83,400.00 and $130,800.00 per year, depending on experience, location, and employer.

What does a remote medical device project manager do?

A Remote Medical Device Project Manager oversees the planning, execution, and completion of projects related to medical devices, all while working remotely. They coordinate cross-functional teams, manage timelines and budgets, ensure regulatory compliance, and communicate with stakeholders to keep projects on track. Their role is crucial for ensuring that new medical devices are developed efficiently and safely, meeting both company goals and industry standards.

What are the key skills and qualifications needed to thrive as a remote medical device project manager?

To thrive as a Remote Medical Device Project Manager, you need strong project management skills, a background in engineering or life sciences, and knowledge of medical device regulations, often supported by a PMP certification or similar credential. Familiarity with project management tools like Microsoft Project, collaboration platforms, and regulatory submission systems (such as FDA eCTD) is commonly required. Exceptional communication, leadership, and problem-solving abilities help in leading cross-functional remote teams and managing stakeholders. These skills are crucial for ensuring regulatory compliance, timely product development, and effective coordination in a dispersed work environment.

What are some common challenges faced by remote medical device project managers, and how can they be addressed?

Remote Medical Device Project Managers often face challenges such as coordinating cross-functional teams across different time zones, maintaining clear communication with stakeholders, and ensuring regulatory compliance from a distance. These challenges can be addressed by establishing regular virtual meetings, using project management tools to track progress, and implementing standardized documentation practices. Building strong relationships with team members and fostering an open communication culture are also key to overcoming these hurdles and ensuring project success.

What is the difference between Remote Medical Device Project Manager vs Remote Medical Device Quality Assurance Specialist?

AspectRemote Medical Device Project ManagerRemote Medical Device Quality Assurance Specialist
CertificationsPMP, CAPM, or equivalent project management certificationsISO 13485 Lead Auditor, CQE, or similar quality assurance certifications
Work EnvironmentOversees project timelines, teams, and deliverables remotely within medical device companiesEnsures compliance, audits, and quality processes remotely in medical device manufacturing or development
Employer & Industry UsageUsed by medical device firms managing product development projects remotelyCommon in companies focusing on quality standards and regulatory compliance remotely

The Remote Medical Device Project Manager focuses on managing project timelines, teams, and deliverables remotely, ensuring successful product development. In contrast, the Remote Medical Device Quality Assurance Specialist concentrates on maintaining quality standards, conducting audits, and ensuring regulatory compliance remotely. Both roles require specialized certifications and are vital in the medical device industry, often working in similar remote environments but with distinct responsibilities.

What job categories do people searching Remote Medical Device Project Manager jobs in Ladera Ranch, CA look for?

The top searched job categories for Remote Medical Device Project Manager jobs in Ladera Ranch, CA are:

What cities near Ladera Ranch, CA are hiring for Remote Medical Device Project Manager jobs?

Cities near Ladera Ranch, CA with the most Remote Medical Device Project Manager job openings:

Remote Medical Device Project Manager jobs near you

Specialist, Clinical Safety (US Remote)

MicroVention

Aliso Viejo, CA

$105K - $131K/yr

Full-time

Re-posted 25 days ago

Job description


Support clinical safety aspects of MicroVention clinical studies. Job duties:
  • Provide all required clinical safety support to assigned clinical studies, including study safety documentation development, adverse events (AE) review, safety investigations, and startup/management of independent safety committees/ adjudicators.
  • Draft, review, and provide input to the clinical safety components of clinical study protocols, study reports, safety manuals, safety CRFs, study supporting materials, and other related documentation.
  • Review and triage study adverse events and prepare for independent physician or committee review by preparing/tabulating these events, gathering relevant source documentation, and preparing narratives.
  • Schedule and manage the proceedings of physician safety committees including Clinical Events Committees (CECs) and Data Safety Monitoring Boards (DSMBs), as well as the activities of independent Clinical Events Adjudicators (CEAs).
  • Support the selection of physician partners, including CEA/CEC/DSMB delegates and other committee members, and provide all required training.
  • Generate and present reports to physician safety committees as well as reports of committee findings and results.
  • Partner with clinical research project managers and Medical Affairs and Safety Manager to ensure safety startup activities and pace of events adjudication aligns with study timeline and milestones and to provide regular progress updates.
  • Support clinical science and regulatory affairs functions by utilizing medical expertise to provide input to study design, clinical evaluation reports, clinical study reports, literature review, risk management, regulatory submissions, questions from regulatory authorities, scientific analyses, and other scientific documentation.
  • Support clinical project management function by utilizing medical expertise to provide input to protocol development, risk/benefit analyses, adverse events review, adverse events reporting, investigator questions, investigator meetings, clinical study reports, and other related documentation/activities.
  • Minimal domestic travel required (1 - 3 trips per year).
  • Comply with applicable Laws and Regulations, adhere to Quality Management System processes and requirements as well as demonstrate Ethics and Integrity in all matters and at all levels throughout the organization.
  • Perform additional duties as assigned.

Qualifications
  1. RN/BSN or equivalent.
  2. Minimum one (1) to three (3) years of experience providing clinical safety support to regulated clinical device studies or relevant clinical research experience, academic experience, or experience in a hospital setting.
  3. Ability to produce high-quality scientific communications and narratives.
  4. Strong written and verbal communication skills.
  5. Strong interpersonal skills to build effective relationships with geographically diverse physicians and internal business partners.
  6. Strong detail-orientation and organizational/time management skills.
  7. Proficiency in standard computer programs including MS Office (Word, Excel, PowerPoint, Outlook, Teams, etc.).
  8. Ability to maintain strict confidentiality.
Desired Qualifications
  1. MD or foreign equivalent.
  2. Clinical, academic, CRO, or industry experience in a relevant field (neurology, neuroradiology, or neurosurgery).
  3. Knowledge of GCP, FDA, and ICH regulations and guidelines.
  4. Knowledge and experience in the detection, understanding, review, investigation, and assessment of adverse events.
  5. Class III medical device safety experience.
Physical
  • Extended periods of computer use.
  • Extended periods of sitting or standing.
  • Light lifting, up to 25 lbs.
  • May be required within the position to be in an environment that can include radiation exposure (such as in Cathlabs).
  • Minimal domestic travel required (1 - 3 trips per year).
EEO
We are an equal employment opportunity employer. All qualified applicants will receive consideration for employment without regard to race, national origin, gender, age, religion, disability, sexual orientation, veteran status, marital status or any other characteristics protected by law.
Fair Chance Ordinance
If you are applying to perform work for Terumo Neuro in any position which will involve performing at least two (2) hours of work on average each week within the unincorporated areas of Los Angeles County, you can find here a list of all material job duties of the specific job position which Terumo Neuro reasonably believes that criminal history may have a direct, adverse and negative relationship potentially resulting in the withdrawal of a conditional offer of employment.
Terumo Neuro will consider for employment qualified job applicants with arrest or conviction records in accordance with the California Fair Chance Act, Los Angeles County Fair Chance Ordinance for Employers, Fair Chance Initiative for Hiring Ordinance, and San Francisco Fair Chance Ordinance.
Salary Range
$105,067 - $131,333 (Financial compensation packages may be higher/lower than listed, & will ultimately depend on factors including relevant experience, internal equity, skillset, knowledge, geography, education, business needs and market demand)

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