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Associate Clinical Manager Jobs in Washington (NOW HIRING)

Senior Clinical Research Associate

Washington, DC ยท On-site +1

$110K - $138K/yr

Senior Clinical Research Associate - Oncology - Washington DC ICON is a global healthcare ... Perform site management activities to support the client's Oncology site success and maintain a ...

Overview Sr. Clinical Research Associate US remotely and on-site (80% travel) Be Part of One Team ... Clinical Study Manager, Lead CRA, Project Manager, etc.) independently schedules and conducts ...

Senior Clinical Research Associate - Cardiovascular Device - Central/West Region ICON is a global ... Ability to work independently and manage multiple priorities in a dynamic environment. * A well ...

Clinical Director

Dumfries, VA ยท On-site

$125K - $135K/yr

Provides clinical supervision and oversight for associate-level and licensed clinical staff in ... Provides leadership, mentorship, training, and performance management to clinical team members

Showing results 41-60

Associate Clinical Manager information

How does an associate clinical manager typically collaborate with cross-functional teams within a healthcare setting?

Associate Clinical Managers often serve as a bridge between clinical staff, administrative teams, and other departments such as quality assurance and human resources. They facilitate effective communication to ensure patient care objectives are met, coordinate schedules or resources, and help implement new protocols or processes. Regular meetings, interdisciplinary rounds, and collaborative problem-solving are common, making strong interpersonal and organizational skills essential for success in this role.

What are the key skills and qualifications needed to thrive as an associate clinical manager, and why are they important?

To thrive as an Associate Clinical Manager, you need a background in healthcare management, clinical expertise, and a relevant degree such as nursing or healthcare administration. Familiarity with clinical information systems, quality assurance protocols, and regulatory compliance tools is typically required. Leadership, problem-solving, and strong interpersonal communication distinguish top performers in this role. These skills ensure effective team management, regulatory adherence, and high standards of patient care in clinical settings.

What is the difference between Associate Clinical Manager vs Clinical Supervisor?

AspectAssociate Clinical ManagerClinical Supervisor
Required CredentialsBachelor's degree in healthcare or related field; some roles may require certificationBachelor's or master's degree in healthcare; relevant licensure or certification often preferred
Work EnvironmentHealthcare facilities, clinics, hospitals, supporting clinical teamsHealthcare settings, overseeing clinical staff and patient care
Employer & Industry UsageHospitals, clinics, healthcare organizations; common in healthcare managementHospitals, outpatient clinics, healthcare organizations; focuses on staff supervision

The Associate Clinical Manager and Clinical Supervisor roles both involve supporting clinical teams in healthcare settings. The Associate Clinical Manager often has broader administrative responsibilities and may be on a pathway to management, while the Clinical Supervisor primarily oversees daily clinical operations and staff. Both roles require relevant healthcare credentials and are integral to patient care quality and team coordination.

Infographic showing various Associate Clinical Manager job openings in Washington as of August 2026, with employment types broken down into 89% Full Time, 10% Part Time, and 1% Contract. Highlights an 77% Physical, 2% Hybrid, and 21% Remote job distribution.

Senior Clinical Research Associate

410 ICR United States USA

Washington, DC โ€ข Hybrid

$110K - $138K/yr

Full-time

Medical, Dental, Vision, Life, Retirement

Re-posted 17 days ago


Job description

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 patients faster.


As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients and suppliers.


The Sr. Clinical Research Associate (Sr. CRA) will be responsible for performing investigative site management and monitoring activities throughout the clinical trial lifecycle. This Sr. CRA role will support the client's Oncology clinical trials to ensure data integrity, subject safety, and inspection readiness at the clinical investigative sites. 

Responsibilities: 

  • Perform site management activities to support the client's Oncology site success and maintain a continuous state of inspection readiness 

  • Act as the primary contact and facilitate efficient communications between the client's clinical trial team and the sites 

  • Perform remote and on-site monitoring/co-monitoring visits (Site Qualification Visits, Site Initiation Visits, Interim Monitoring Visits and Close-Out Visits) to ensure data integrity and subject safety in the client's trials 

  • May perform oversight activities to assess monitoring quality and train/mentor less experienced CRAs 

  • Promptly document monitoring activities and submit/approve visit reports  

  • Manage site essential document collection and TMF reconciliation with site files 

  • Support sites with local Institutional Review Board (IRB)/Ethics Committee (EC) submissions and confirm approvals 

  • Regularly review site Key Risk Indicator (KRI) metrics, issues and action items to detect trends and ensure prompt resolution 

  • Independently determine root causes and develop/implement site Corrective Action and Preventive Action (CAPA) plans 

  • Deliver training to ensure sites comply with the protocol, Standard Operating Procedures (SOPs), Good Clinical Practices (GCPs) and regulations 

  • Support sites and the client's regulatory inspections 

  • Contribute to site identification; drive site feasibility and qualification progress; and support site activation activities  

  • Lead site engagement initiatives and foster relationships with key Oncology sites and networks  

Qualifications 

  • Bachelor’s degree (scientific field preferred) 

  • 5+ years monitoring clinical trials independently conducting on-site and remote monitoring visits. Atleast 2 years monitoring solid tumor clinical trials.

  • 1+ years early development trial experience  

  • Solid tumor clinical trial experience is required

  • Experience utilizing Veeva systems is highly preferred 

  • Demonstrated experience developing/maintaining site relationships and securing compliance 

  • Expertise in GxPs and Oncology monitoring techniques (including Risk-Based Monitoring) and terminology 

  • Experience collaborating with sites from initial engagement through close-out phases 

  • Experience activating sites 

  • Experience training site staff 

  • Experience supporting sites and/or sponsors in regulatory inspections 

  • Experience working within a Functional Services (or in-house) monitoring model is preferred 

  • Willing to travel up to 50% 


Employment with ICON is contingent upon having the legal right to work in the country where the role is based.


Rewards & Benefits

ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development.


Benefits may include:

  • Competitive base salary and performance related incentives
  • Health and wellbeing programmes including medical, dental, and vision coverage where applicable
  • Retirement and pension plans
  • Life assurance and disability coverage
  • Employee assistance programmes and wellbeing resources
  • Learning and development opportunities through structured training and career pathways

Benefits may vary depending on role and location.


Visit our careers site to read more about the benefits ICON offers.


Inclusion and Accessibility

ICON is an equal opportunity employer. We are committed to building an inclusive and accessible workplace where everyone feels valued and supported.


If you require reasonable accommodations during the recruitment process, please let us know or submit a request here.

Salary Range

$110,520.00-$138,150.00

Are you a current ICON Employee? Please click here to apply