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Director Virtual Clinical Research Jobs (NOW HIRING)

Alnylam Pharmaceuticals

Director, Clinical Research

Cambridge, MA · On-site

$255K - $345K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

The Director, Clinical Research, will work in a matrix organization across Regulatory, Biostatistics, Clinical Operations, Preclinical, Commercial & Quality Assurance teams to ensure fully harmonized ...

Alcanza Clinical Research

Clinical Research Coordinator

Methuen, MA

$25.25 - $33.75/hr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

The Clinical Research Coordinator under the direction of the Site Manager/Director and the Principal/Sub Investigators conducts the following according to the study protocol, company processes ...

Alcanza Clinical Research

$23.50 - $31.25/hr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

The Clinical Research Coordinator under the direction of the Site Manager/Director and the Principal/Sub Investigators conducts the following according to the study protocol, company processes ...

Actalent

Clinical Research Program Director

Bronx, NY · On-site

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Program Director - Early Phase Clinical Research The Program Director leads training and onboarding for new study coordinators and oversees the operational and financial aspects of an early phase ...

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Director Virtual Clinical Research information

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How much do director virtual clinical research jobs pay per hour?

As of Aug 13, 2026, the average hourly pay for director virtual clinical research in the United States is $54.33, according to ZipRecruiter salary data. Most workers in this role earn between $32.45 and $71.63 per hour, depending on experience, location, and employer.

What is the difference between Director Virtual Clinical Research vs Clinical Project Manager?

AspectDirector Virtual Clinical ResearchClinical Project Manager
CredentialsTypically requires a Bachelor's or Master's in life sciences, clinical research, or related field; certifications like CCRP or RAC are commonSimilar credentials, often with a background in clinical research or life sciences; certifications like PMP are advantageous
Work EnvironmentLeads virtual teams, oversees multiple projects, and interacts with sponsors remotelyManages specific clinical trials, often in a team setting, with some remote work but more site visits
Employer & Industry UsageUsed by pharmaceutical, biotech, and CRO companies for strategic oversightCommonly employed by CROs and pharmaceutical companies for trial execution

The main difference is that the Director Virtual Clinical Research focuses on strategic leadership and oversight of multiple virtual clinical trials, while the Clinical Project Manager handles the day-to-day management of individual clinical studies. Both roles require similar credentials and industry experience, but their scope and responsibilities differ significantly.

More about Director Virtual Clinical Research jobs
What cities are hiring for Director Virtual Clinical Research jobs? Cities with the most Director Virtual Clinical Research job openings:
What are the most commonly searched types of Virtual Clinical Research jobs? The most popular types of Virtual Clinical Research jobs are:
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Director Virtual Clinical Research jobs near you
Infographic showing various Director Virtual Clinical Research job openings in the United States as of August 2026, with employment types broken down into 3% As Needed, 72% Full Time, 17% Part Time, and 8% Contract. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution, with an average salary of $113,010 per year, or $54.3 per hour.

Clinical Research Nurse

Tandem Clinical Research

Marrero, LA • On-site

Other

Re-posted 13 days ago

Job description

The Clinical Research Nurse oversees the daily activities of clinical research studies. They
work closely with the clinical teams and investigators to ensure that all required
procedures and visits occur according to protocol specific guidelines.
RESPONSIBILITIES

  • Understand thoroughly all assigned studies through reading protocols, attending investigator meetings and start-up meetings, and coordinating with Principal Investigator
  • Adhere strictly to the study protocol; obtain exemptions when necessary/appropriate
  • Communicate protocol issues to CRO and/or Sponsor, Site Administrator, Director, Principal or Sub-Investigator
  • Articulate all pertinent issues to the PI or document by email/letter or during meetings
  • Collect initial psychiatric and medical information by interviewing patients and by accessing other appropriate sources
  • Ensure a flow of communication including telephone conferences between patient, study staff, referral sources, Sponsor and/or CRO, Monitor(s), Auditors and any marketing groups hired by the Sponsor
  • Utilize various rating scales and maintain interrater reliability with other clinicians
  • Perform clinical tasks including, but not limited to, vital signs, height and weight, ECG, phlebotomy, specimen packaging
  • Maintain timely source documentation as well as sponsor required information.
  • Dispense and maintain accurate records of study medication
  • Educate patients and family regarding their particular study and clinical drug trials in general.
  • Complete all monitor and sponsor queries in a timely manner
  • Provide appropriate community resource referrals to patients, caretakers, and family at conclusion of patient's participation in study
Requirements
  • Ability to communicate clearly and effectively (written and verbal)
  • Ability to communicate in an active multi-office environment
  • Must possess excellent interpersonal and customer service skills
  • Ability to multi-task, organize, prioritize appropriately, and work well both individually and as part of a team
  • Ability to use time productively and contribute to high levels of company operational efficiency and effectiveness
  • Ability to maintain confidentiality of information
  • Ability to efficiently operate all job-related office equipment (telephone, computer, calculator, fax, copier, study-specific equipment)
Required Experience
  • Bachelor's degree required
  • RN licensure
  • Experience as a Clinical Research Coordinator (CRC) or Research Assistant

Apply