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Remote Operations Research Jobs in Maryland (NOW HIRING)

  • Medical

  • Life

Summary: The Senior Clinical Research Associate (Sr. CRA) is an experienced clinical operations ... remote). * Actively participate in site feasibility assessments and site selection processes.

New

Clinical Research Associate II

Rockville, MD · On-site +1

  • Medical

  • Retirement

CRA, Project Manager, etc., independently schedules and conducts remote and on-site monitoring ... Knowledgeable in clinical research operations, including interpretation and implementationof ...

Senior Data Scientist

Fort George G Meade, MD · On-site +1

$150K - $220K/yr

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

Meade Posting Date 07/24/2026 Security Clearance Required - TS/SCI + Poly Remote Type N/A Time Type ... Conduct assessments of clients' preparedness to integrate data analytics into their operations ...

Senior Data Scientist

Fort George G Meade, MD · On-site +1

$150K - $220K/yr

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

Meade Posting Date 07/24/2026 Security Clearance Required - TS/SCI + Poly Remote Type N/A Time Type ... Conduct assessments of clients' preparedness to integrate data analytics into their operations ...

Senior Project Manager

Indian Head, MD · On-site +1

$135K - $150K/yr

... research and development capabilities and ongoing production operations. Candidates must be eager ... This position does not allow for a remote or hybrid work schedule. As a Senior Project Manager at ...

DevOps Engineer

Bethesda, MD · On-site +1

$170 - $225K/hr

  • Medical

  • Retirement

  • PTO

... research and development cycles. Have impact as part of a mission-focused, solutions-oriented, and ... Percentage of remote work will vary based on client requirements/deliverables. Responsibilities ...

$79K - $107K/yr

Remote - US Interested applicants must reside in one of the following approved states: Arizona ... operational excellence. This role is meaningful because you will transform the way millions of ...

Showing results 21-40

Remote Operations Research information

What is the difference between Remote Operations Research vs Remote Data Analyst?

AspectRemote Operations ResearchRemote Data Analyst
Required CredentialsAdvanced degree in Operations Research, Mathematics, or related fieldBachelor's or Master's in Data Science, Statistics, or related field
Work EnvironmentCollaborative teams, often in consulting or corporate settings, with complex problem-solvingData-focused roles in various industries, analyzing datasets to inform decisions
Industry UsageLogistics, manufacturing, supply chain, consultingFinance, marketing, healthcare, technology
Common Search/ComparisonRemote Operations ResearchRemote Data Analyst

Remote Operations Research involves applying advanced analytical methods to optimize complex systems, often requiring specialized degrees. Remote Data Analysts focus on interpreting data to support business decisions, with a broader range of educational backgrounds. Both roles are in high demand and often work remotely across various industries, but they differ in scope and technical depth.

What are the most commonly searched types of Operations Research jobs in Maryland?

The most popular types of Operations Research jobs in Maryland are:

What are popular job titles related to Remote Operations Research jobs in Maryland?

For Remote Operations Research jobs in Maryland, the most frequently searched job titles are:

What job categories do people searching Remote Operations Research jobs in Maryland look for?

The top searched job categories for Remote Operations Research jobs in Maryland are:

What cities in Maryland are hiring for Remote Operations Research jobs?

Cities in Maryland with the most Remote Operations Research job openings:

Infographic showing various Remote Operations Research job openings in Maryland as of June 2026, with employment types broken down into 76% Full Time, and 24% Part Time. Highlights an 100% Remote job distribution.

Director of Quality Assurance - REMOTE

i4 Search Group Healthcare

Baltimore, MD • Remote

$80K - $100K/yr

Full-time

Medical, Dental, Vision, Retirement, PTO

Re-posted 5 days ago


Job description

Job Description: Director of Quality Assurance


Location: Remote (U.S.-Based) - Any Location

Employment Type: Full-Time


Position Summary

We are seeking an experienced and detail-oriented Director of Quality Assurance to lead regulatory operations supporting clinical research activities. This role will oversee a team of Clinical Research Coordinators (CRCs) and regulatory staff while ensuring compliance with federal regulations, sponsor requirements, institutional policies, and Good Clinical Practice (GCP) guidelines.

The Regulatory Affairs Supervisor will serve as a key liaison between investigators, sponsors, contract research organizations (CROs), and regulatory agencies to support the successful execution of clinical trials from study startup through closeout.


Key Responsibilities

Regulatory Leadership & Oversight

  • Supervise and mentor regulatory coordinators and Clinical Research Coordinators (CRCs).
  • Ensure compliance with FDA regulations, ICH-GCP guidelines, HIPAA requirements, and institutional policies.
  • Oversee preparation, submission, and maintenance of regulatory documents for clinical trials.
  • Manage regulatory activities throughout the study lifecycle, including startup, amendments, continuing reviews, reportable events, and study closeout.
  • Maintain regulatory binders, essential documents, and study files to ensure audit readiness.


Clinical Trial Management Support

  • Collaborate with Principal Investigators, study teams, sponsors, and CROs to facilitate regulatory compliance and study execution.
  • Review study protocols, informed consent documents, investigator brochures, and sponsor communications.
  • Support site initiation, monitoring, audit, and closeout activities.
  • Track regulatory milestones and ensure timely submissions and approvals.


Team Supervision

  • Provide leadership, training, onboarding, and performance management for CRCs and regulatory personnel.
  • Establish workload priorities and ensure timely completion of regulatory deliverables.
  • Develop standard operating procedures (SOPs) and best practices to improve operational efficiency.
  • Foster a culture of quality, accountability, and continuous improvement.


Quality & Compliance

  • Conduct internal audits and quality reviews of study documentation.
  • Identify compliance risks and implement corrective and preventive actions (CAPAs).
  • Serve as a regulatory subject matter expert during sponsor audits, FDA inspections, and institutional reviews.
  • Monitor regulatory changes and communicate updates to research staff.


Required Qualifications

  • Bachelor's degree in Life Sciences, Healthcare Administration, Public Health, Nursing, Pharmacy, or related field.
  • 5+ years of experience supporting clinical research and regulatory affairs.
  • 2+ years of supervisory or team leadership experience.
  • Strong knowledge of:
  • FDA regulations
  • ICH-GCP guidelines
  • Human Subjects Protection requirements
  • IRB processes
  • Clinical trial operations
  • Experience managing regulatory submissions for multiple clinical studies.
  • Excellent organizational, communication, and project management skills.


Preferred Qualifications

  • Certified Clinical Research Professional (CCRP), Certified Clinical Research Coordinator (CCRC), or equivalent certification.
  • Experience with oncology, device, pharmaceutical, or multisite clinical trials.
  • Familiarity with CTMS, eRegulatory systems, and electronic document management platforms.
  • Experience supporting FDA inspections and sponsor audits.


Benefits

  • Fully remote work environment
  • Competitive salary
  • Medical, dental, and vision insurance
  • Paid time off and holidays
  • 401(k) with company match
  • Professional development opportunities
  • Career growth within a collaborative research organization


Ideal Candidate:

The ideal candidate is a proactive regulatory professional with strong clinical research experience who enjoys leading teams, ensuring compliance, and supporting high-quality clinical trial execution in a fast-paced remote environment.