
ClinicalTrials.gov Specialist
At Wentworth-Douglass Hospital, we believe in providing our patients with the highest quality of care, which is why we are seeking a highly motivated and detail-oriented individual to join our team as a ClinicalTrials.gov Specialist. In this role, you will play a crucial role in ensuring the accuracy and compliance of our clinical trial data on the widely recognized platform, ClinicalTrials.gov. We are looking for someone who is passionate about improving healthcare through clinical research and has a strong understanding of regulatory requirements. If you are a highly organized and collaborative individual with excellent communication skills, we encourage you to apply for this exciting opportunity to make a meaningful impact on patient care.
- Effectively manage and maintain all clinical trial information on ClinicalTrials.gov, ensuring accuracy and compliance with regulatory requirements
- Collaborate with clinical research team to gather and review necessary data for ClinicalTrials.gov submissions
- Monitor and track changes in regulations and requirements for ClinicalTrials.gov, and implement necessary updates to ensure compliance
- Provide guidance and training to clinical research team on ClinicalTrials.gov processes and best practices
- Serve as a liaison between Wentworth-Douglass Hospital and external partners, such as pharmaceutical companies and research organizations, to ensure timely and accurate submission of clinical trial information
- Conduct regular audits of clinical trial data on ClinicalTrials.gov to identify and address any discrepancies or issues
- Stay up-to-date on industry trends and advancements in clinical research to continuously improve processes and ensure best practices are being followed
- Communicate effectively with internal and external stakeholders to provide updates and address any questions or concerns related to ClinicalTrials.gov
- Work closely with regulatory agencies and other governing bodies to ensure compliance with all regulations and guidelines related to clinical trials and data submissions
- Participate in relevant meetings and trainings to stay informed and contribute to the overall success of the clinical research team and hospital.
Bachelor's Degree In A Related Field Such As Healthcare Administration, Public Health, Or Clinical Research.
Minimum Of 2 Years Of Experience In Clinical Research And Knowledge Of Clinical Trial Regulations And Guidelines.
Certification In Clinical Research (Ccrp) Or Clinical Research Coordinator (Ccrc) Preferred.
Strong Organizational And Project Management Skills With The Ability To Prioritize And Manage Multiple Tasks Efficiently.
Excellent Communication And Interpersonal Skills, With The Ability To Work Collaboratively With A Diverse Team Of Healthcare Professionals, Researchers, And Patients.
Quality Assurance
Data Analysis
Budget management
Data Management
Regulatory compliance
Patient Recruitment
Protocol Development
Informed Consent
Protocol Interpretation
Investigator Communication
Clinical Trial Tracking
Communication
Conflict Resolution
Leadership
Time management
creativity
flexibility
Teamwork
collaboration
Adaptability
Problem-Solving
According to JobzMall, the average salary range for a ClinicalTrials.gov Specialist in Boston, MA, USA is $60,000-$80,000 per year. However, this can vary depending on the specific company, level of experience, and other factors such as education and certifications. Some higher-paying roles may offer salaries upwards of $100,000 per year.
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Wentworth-Douglass Hospital is the Seacoast's leading not-for-profit medical center with comprehensive services including walk-in care & physician practices. Hospital includes 178-bed Magnet® Recognized hospital, several urgent care and walk-in care facilities, multiple testing centers, 36 Wentworth Health Partners primary care and specialty care provider practices, The Works Health and Fitness Center and the Wentworth-Douglass Foundation.

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