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Remote Ppd Clinical Research Jobs in Silver Spring, MD

Emmes

Senior Clinical Research Associate

Rockville, MD · On-site +1

... conducts remote and on site monitoring visits such as qualification/pre study visits, site ... Expertise in clinical research operations, including interpretation and implementation of country ...

ICON

Senior Clinical Research Associate

Washington, DC · On-site +1

$110K - $138K/yr

Senior Clinical Research Associate - Oncology - Washington DC ICON is a global healthcare ... Perform remote and on-site monitoring/co-monitoring visits (Site Qualification Visits, Site ...

Emmes

Sr. Clinical Research Associate

Rockville, MD · On-site +1

... conducts remote and on site monitoring visits such as qualification/pre study visits, site ... Expertise in clinical research operations, including interpretation and implementation of country ...

ICON

Senior Clinical Research Associate

Baltimore, MD · On-site +1

Senior Clinical Research Associate - Oncology - Baltimore, MD or Phila, PA ICON is a global health ... Perform remote and on-site monitoring/co-monitoring visits (Site Qualification Visits, Site ...

Emmes

Clinical Research Associate II

Rockville, MD · On-site +1

Overview Clinical Research Associate II US remotely and on-site (80% travel) Emmes Group: Building ... CRA, Project Manager, etc., independently schedules and conducts remote and on-site monitoring ...

Emmes

Clinical Research Associate II

Rockville, MD · On-site +1

Overview Clinical Research Associate II US remotely and on-site (80% travel) Be Part of One Team ... conducts remote and on-site monitoring visits such as qualification pre study visits, site ...

IQVIA

Clinical Trial Rater

Washington, DC · Remote

Flexible, remote work schedule. * Opportunity to contribute to global clinical research. * Collaborate with a team committed to improving patient care and advancing science. #LI-DNP #LI-Remote #LI ...

Emmes

Sr. In-House CRA

Rockville, MD · On-site +1

At Emmes Group , we're shaping the future of clinical research- where human intelligence meets ... May perform remote review and monitoring of Informed Consent Forms and other source documents.

IQVIA

Clinical Trial Psych Rater

Fairfax, VA · Remote

$62K - $156K/yr

Remote/Virtual Hours: Estimated 10-16 hours per month Role: Clinical Specialist About IQVIA IQVIA is a global leader in advanced analytics, technology solutions, and clinical research services ...

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Remote Ppd Clinical Research information

See Silver Spring, MD salary details

$50.7K

$111K

$195.4K

How much do remote ppd clinical research jobs pay per year?

As of Aug 21, 2026, the average yearly pay for remote ppd clinical research in Silver Spring, MD is $110,962.00, according to ZipRecruiter salary data. Most workers in this role earn between $83,700.00 and $126,600.00 per year, depending on experience, location, and employer.

What is a remote PPD Clinical Research professional?

A Remote PPD Clinical Research job involves working for PPD (Pharmaceutical Product Development), a global contract research organization, to support clinical trials and research projects from a remote location. Professionals in this role help design, manage, and monitor clinical studies to ensure compliance with protocols, regulatory standards, and data integrity. Responsibilities may include data management, coordinating with study sites, and supporting trial documentation. Working remotely allows employees to collaborate with international teams and clients while maintaining flexibility. This role is essential in advancing new treatments and therapies to market efficiently and safely.

How does working remotely as a PPD Clinical Research professional impact collaboration with on-site teams and study sites?

As a remote PPD Clinical Research professional, you will collaborate closely with on-site teams, investigators, and study coordinators through virtual communication platforms. While you may not be physically present, regular video calls, emails, and project management tools are used to maintain effective communication and ensure study protocols are followed. Adapting to different time zones and proactively addressing challenges in real-time are common aspects of the role. Strong organizational and interpersonal skills are essential for building trust and maintaining seamless coordination across dispersed teams.

What are the key skills and qualifications needed to thrive as a remote PPD Clinical Research professional?

To excel as a Remote PPD Clinical Research professional, you need a comprehensive understanding of clinical trial processes, regulatory guidelines (such as GCP), and a relevant degree in life sciences or a related field. Familiarity with electronic data capture (EDC) systems, remote monitoring tools, and certifications like ACRP or SOCRA are typically valuable. Strong organizational skills, attention to detail, and effective communication are crucial soft skills for managing studies and collaborating with distributed teams. These competencies ensure compliance, data integrity, and the successful execution of clinical research in a remote environment.

What are the most commonly searched types of Ppd Clinical Research jobs in Silver Spring, MD?

The most popular types of Ppd Clinical Research jobs in Silver Spring, MD are:

What are popular job titles related to Remote Ppd Clinical Research jobs in Silver Spring, MD?

For Remote Ppd Clinical Research jobs in Silver Spring, MD, the most frequently searched job titles are:

What job categories do people searching Remote Ppd Clinical Research jobs in Silver Spring, MD look for?

The top searched job categories for Remote Ppd Clinical Research jobs in Silver Spring, MD are:

What cities near Silver Spring, MD are hiring for Remote Ppd Clinical Research jobs?

Cities near Silver Spring, MD with the most Remote Ppd Clinical Research job openings:

Remote Ppd Clinical Research jobs near you

Clinical Research Assistant

Allen Spolden

Silver Spring, MD • Remote

$45K - $55K/hr

Full-time

Medical, Dental, Vision, Retirement, PTO

Posted 29 days ago

Job description

This is a remote position.

Position Overview

We are seeking a motivated and detail-oriented Clinical Research Assistant to join our growing clinical operations team. In this role, you will support the coordination and administration of clinical research studies while ensuring study documentation, data quality, and regulatory compliance are maintained throughout the research process.

This position is ideal for someone with excellent organizational skills, strong attention to detail, and an interest in contributing to clinical research in a remote environment.

Essential Responsibilities
  • Assist with the day-to-day management of assigned clinical studies.
  • Maintain investigator site files, regulatory binders, and essential study documents.
  • Prepare, review, and file research documentation in accordance with study requirements.
  • Support participant scheduling and study visit coordination.
  • Enter, verify, and reconcile clinical data within electronic research systems.
  • Monitor study timelines and assist with tracking project deliverables.
  • Communicate effectively with investigators, sponsors, study participants, and internal research teams.
  • Identify and escalate documentation discrepancies or protocol deviations when appropriate.
  • Ensure research activities are conducted in compliance with ICH Good Clinical Practice (GCP), study protocols, and applicable regulatory requirements.
  • Perform additional administrative and research support duties as assigned.


RequirementsQualifications
Required
  • Bachelor's degree in Life Sciences, Health Sciences, Nursing, Public Health, or a related discipline, or equivalent healthcare experience.
  • Strong organizational and problem-solving abilities.
  • Excellent verbal and written communication skills.
  • High level of accuracy and attention to detail.
  • Proficiency with Microsoft Office and web-based software applications.
  • Ability to manage multiple priorities while working independently in a remote setting.
Preferred
  • Previous experience supporting clinical research or healthcare operations.
  • Familiarity with ICH-GCP guidelines and FDA regulations.
  • Experience using Electronic Data Capture (EDC), CTMS, or eTMF systems.
  • Knowledge of clinical trial documentation and research workflows.
Work Schedule
  • Full-time
  • Monday through Friday
  • Standard business hours


BenefitsBenefits
  • Competitive salary
  • Comprehensive medical, dental, and vision coverage
  • 401(k) with employer contribution
  • Paid time off and company holidays
  • Remote work environment
  • Professional development and career advancement opportunities