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Senior Clinical Research Associate Jobs (NOW HIRING)

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 intelligence and clinical research organisation united by a mission to bring new medicines and treatments to ...

Icon plc

Senior Clinical Research Associate

San Diego, CA · Hybrid

$110K - $138K/yr

Senior Clinical Research Associate - Oncology - Southern California ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and ...

Icon plc

Senior Clinical Research Associate

Washington, DC · Hybrid

$110K - $138K/yr

Senior Clinical Research Associate - Oncology - Washington DC ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to ...

WEP Clinical

Senior Clinical Research Associate

The WEP Clinical Senior Clinical Research Associate (Senior CRA) oversees all aspects of clinical monitoring and site management in compliance with GCP, global regulatory requirements, and WEP ...

Emmes

Senior Clinical Research Associate

Rockville, MD · On-site +1

Overview Senior Clinical Research Associate US Remote Emmes Group: Building a better future for us all. Emmes Group is transforming the future of clinical research, bringing the promise of new ...

Getinge

Sr. Clinical Research Associate

Boston, MA · Hybrid

$125K/yr

The Senior Clinical Research Associate is responsible for oversight of the prospective randomized clinical studies conducted by Paragonix Technologies. This position is responsible for managing ...

Getinge

Sr. Clinical Research Associate

Boston, MA · On-site

$125K/yr

The Senior Clinical Research Associate is responsible for oversight of the prospective randomized clinical studies conducted by Paragonix Technologies. This position is responsible for managing ...

Emmes

Sr. Clinical Research Associate

Rockville, MD

Overview Sr. Clinical Research Associate Be Part of One Team, One Purpose. At Emmes Group , we're shaping the future of clinical research- where human intelligence meets cutting-edge technology to ...

PSI CRO

Senior Clinical Research Associate

As a Senior Clinical Research Associate you will work on the frontline of communication with project stakeholders, ensuring timelines, targets and standards of clinical research projects in a variety ...

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Senior Clinical Research Associate information

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$36K

$94.3K

$143.5K

How much do senior clinical research associate jobs pay per year?

As of Jul 24, 2026, the average yearly pay for senior clinical research associate in the United States is $94,314.00, according to ZipRecruiter salary data. Most workers in this role earn between $62,500.00 and $128,000.00 per year, depending on experience, location, and employer.

How much does a CRA II make at Icon?

A CRA II (Clinical Research Associate II) at Icon typically earns between $70,000 and $90,000 annually, depending on experience, location, and certifications. Compensation may also include bonuses and benefits related to clinical trial monitoring and site management.

What is the role of a senior clinical research associate?

A senior clinical research associate (CRA) oversees the conduct of clinical trials to ensure compliance with protocols, Good Clinical Practice (GCP), and regulatory requirements. They monitor trial sites, review data quality, and coordinate with investigators, often using electronic data capture systems, and typically require relevant certifications and experience in clinical research. Their role is essential for maintaining trial integrity and ensuring timely study completion.

What are the key skills and qualifications needed to thrive as a Senior Clinical Research Associate, and why are they important?

To thrive as a Senior Clinical Research Associate, you need a solid background in clinical research, regulatory compliance, and often a degree in life sciences or a related field. Familiarity with electronic data capture (EDC) systems, Good Clinical Practice (GCP) guidelines, and relevant certifications such as ACRP or SOCRA are typically required. Strong organizational skills, attention to detail, and the ability to communicate effectively with diverse stakeholders make someone stand out in this position. These skills and qualities are vital for ensuring studies are conducted ethically, accurately, and in compliance with regulatory standards.

What is the highest paying job in clinical research?

In clinical research, senior roles such as Director of Clinical Operations or Clinical Program Manager typically have the highest salaries, often exceeding $150,000 annually. These positions require extensive experience, leadership skills, and often advanced certifications or degrees in related fields.

What Does a Senior Clinical Research Associate Do?

A senior clinical research associate (CRA) monitors clinical trials and manages team members. Your duties include leading project team meetings, running experiments, making observations, tracking results, and analyzing data. You also ensure experiments meet all clinical practice and safety standards. Qualifications for this career are a bachelor of science in a biomedical field or a bachelor of science in nursing (BSN), along with professional experience in a medical or research setting. You must have strong communication, interpersonal, leadership, and technical writing skills.

How much does a senior CRA make at Iqvia?

A Senior Clinical Research Associate (CRA) at IQVIA typically earns between $80,000 and $110,000 annually, depending on experience, location, and certifications. The role often requires monitoring clinical trials, ensuring compliance, and working with clinical data management tools.

What are some typical challenges faced by Senior Clinical Research Associates when overseeing multiple clinical trials?

Senior Clinical Research Associates (SCRAs) often manage several studies at once, which requires balancing competing deadlines, ensuring protocol compliance, and maintaining strong communication with site staff. A common challenge is ensuring consistent data quality and regulatory adherence across diverse sites, especially when trials are geographically dispersed. Effective time management, attention to detail, and proactive problem-solving are crucial for success in this role. Collaboration with project managers, investigators, and regulatory teams is also essential to ensure trials progress smoothly and meet all regulatory requirements.

What is a Senior Clinical Research Associate?

A Senior Clinical Research Associate (Senior CRA) is an experienced professional responsible for overseeing and monitoring clinical trials to ensure compliance with regulatory requirements, protocols, and good clinical practice. They often serve as a liaison between the sponsor and clinical sites, ensuring data integrity and patient safety. Senior CRAs may also mentor junior staff, manage multiple studies, and resolve complex issues that arise during trials. Their work is critical in bringing new medical treatments and devices to market safely and efficiently.
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Senior Clinical Research Associate jobs near you
Infographic showing various Senior Clinical Research Associate job openings in the United States as of July 2026, with employment types broken down into 1% As Needed, 69% Full Time, 28% Part Time, 1% Temporary, and 1% Contract. Highlights an 97% Physical, 1% Hybrid, and 2% Remote job distribution, with an average salary of $94,314 per year, or $45.3 per hour.
Senior Clinical Research Associate - CNS

Senior Clinical Research Associate - CNS

Cognitive Research Corporation

Remote

Full-time

Posted 16 days ago

Job description

The Senior Clinical Research Associate is responsible for overseeing the execution of clinical trials at Investigative Sites. The Clinical Research Associate acts as a liaison between the study Sponsor, CRC and Investigative Sites. They will proactively identify and resolve clinical project issues and participate in process improvement initiatives as applicable. The CRA facilitates successful execution of studies by Investigative Sites and helps to ensure the rights, safety and welfare of human research participants as well as data integrity in clinical trials.
Essential Duties & Responsibilities
  • Initiates, monitors, and closes-out investigative sites in accordance with FDA/ICH regulations.
  • Tracks and maintains study specific non-Case Report Form database
  • Administers Clinical research projects; collects investigator documentation, site management, clinical contact, and prepare reports as required
  • Ensures appropriate source document review and source document verification as required
  • Reviews Case Report Forms to identify erroneous, missing, or incomplete data
  • Generates queries to resolve problematic data to appropriate personnel, and review responses to assure the database is updated accordingly
  • Verifies study drug accountability; generates and tracks drug shipments and storage
  • Travels as necessary, based on project needs and according to Clinical Monitoring Plan requirements
  • Performs data collection, retrieval, entry and clean up as necessary
  • Develops and maintains strong relationships with Investigator(s) and site staff
  • Independently manages sites resulting in acceptable Quality Assurance reports.
  • Escalates study/site issues/deviations appropriately
  • Serves as lead monitor for a protocol or project by creating study files, arranges monitoring schedules, leads the project team, organize and run meetings and performs other project management duties as assigned by management
  • Writes Clinical Trial Reports, analyzing and presenting trial results in a clear and accurate format
  • Reports, writes narratives, and follows-up on reported serious adverse events
  • Interacts and attends client meetings, as appropriate
  • Mentors junior staff/CRAs
  • Quality oversight checks of monitoring
  • Performs other duties as assigned

Qualifications
  • Bachelor's degree, or RN, in a related field or equivalent combination of education, training and experience
  • Minimum 5 years' experience as a CRA; experience overseeing clinical trials in the pharmaceutical, hospital or CRO industry
  • Ability to work and travel independently with minimal supervision
  • Experience with numerous EDC systems.
  • Advanced knowledge of GCPs, ICH guidelines, FDA and other applicable regulations
  • Specialized knowledge of CNS therapeutic areas
  • Proficiency in Microsoft Office, Zoom and Adobe
  • Excellent writing and verbal skills, English language proficiency
  • Meticulous attention to detail
  • Time management and ability to prioritize tasks
  • Ability to travel up to 70%

Department Clinical Operations Role Senior Clinical Research Associate Locations Remote, US Remote status Fully Remote Employment type Full-time

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