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  1. Home
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  5. Clinical Trial Monitor II
Dana-Farber Cancer Institute logo

Clinical Trial Monitor II

Not Disclosed•Full-TimeOn-site

location_on143, Bolton Street, Dorchester Heights, South Boston, Boston, Suffolk County, Massachusetts, 02127, United States

Apply Now

About Dana-Farber Cancer Institute

Located in Boston and the surrounding communities, Dana-Farber Cancer Institute is a leader in life-changing breakthroughs in cancer research and patient care. We are united in our mission of conquering cancer, HIV/AIDS, and related diseases. We strive to create an inclusive, diverse, and equitable environment where we provide compassionate and comprehensive care to patients of all backgrounds, and design programs to promote public health particularly among high-risk and underserved populations. We conduct groundbreaking research that advances treatment, educate tomorrow's physician-researchers, and work with amazing partners, including other Harvard Medical School-affiliated hospitals.

At Dana-Farber, we work every day to create an innovative, caring, and inclusive environment where every patient, family, and staff member feels they belong. As relentless as we are in our mission to reduce the burden of cancer for all, we are committed to having faculty and staff who offer multifaceted experiences. Cancer knows no boundaries, and when it comes to hiring the most dedicated and compassionate professionals, neither do we. If working in this kind of organization inspires you, we encourage you to apply.

About the Role

The Clinical Trials Monitor plays a vital role in ensuring the compliance of the clinical research enterprise with all related regulatory policies and guidelines, including federal, state, local, and the policies outlined by the Dana-Farber Cancer Institute and Dana-Farber Harvard Cancer Center (DF/HCC) consortium. Under the direction of Clinical Trials Office Leadership, you will assist in the design, development, implementation, and conduct of an effective monitoring program in accordance with Good Clinical Practice, institutional policies, and research protocols.

In this position, you will ensure that appropriate monitoring tasks and activities occur as outlined in the monitoring plan for assigned clinical trials. Your work will involve a combination of remote data review and onsite monitoring visits, requiring a willingness and ability to travel occasionally. You will manage multiple projects simultaneously, balancing strong time management skills with the ability to work both independently and as part of a team. A key part of your mission will be promoting a culture of monitoring compliance and regulatory awareness within the organization.

Hiring Process

We are committed to a fair and transparent hiring process. For union positions, the pay range is determined by the Collective Bargaining Agreement (CBA). For other roles, the hiring range is based on market pay structures, with individual salaries determined by factors such as business needs, market conditions, internal equity, and the candidate's relevant experience, skills, and qualifications.

Equal Opportunity Employer

Dana-Farber Cancer Institute is an equal opportunity employer and affirms the right of every qualified applicant to receive consideration for employment without regard to race, color, religion, sex, gender identity or expression, national origin, sexual orientation, genetic information, disability, age, ancestry, military service, protected veteran status, or other characteristics protected by law.

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Skills, education and keywords

Skills: Good Clinical Practice, Ich/gcp, Fda Regulations, Source Data Verification, Microsoft Office, Word, Excel, Powerpoint.

Education: Bachelor's degree in a field related to research compliance required.

Frequently asked questions about Clinical Trial Monitor II at Dana-Farber Cancer Institute

What does a Clinical Trial Monitor II at Dana-Farber Cancer Institute do?expand_more
Day-to-day, the Clinical Trial Monitor II at Dana-Farber Cancer Institute will ensure sponsor-investigator and study teams adhere to fda regulations and ich/gcp guidelines; monitor clinical trial progress through remote data review and onsite visits; provide guidance to monitoring teams and assist in audit readiness preparation; and assist in training and orienting newly hired clinical trials monitors.
What are the requirements for this Clinical Trial Monitor II role?expand_more
To qualify for the Clinical Trial Monitor II at Dana-Farber Cancer Institute position, applicants should have: Bachelor's degree in a field related to research compliance; 5 years of clinical trials experience; 3+ years of monitoring experience; Knowledge of federal, state and local regulations; Experience interpreting legislation, regulations, policies, procedures, and ethical principles; and Ability to translate regulations into operational policies and procedures.
Where is the Clinical Trial Monitor II role at Dana-Farber Cancer Institute located?expand_more
Clinical Trial Monitor II at Dana-Farber Cancer Institute is based in 143, Bolton Street, Dorchester Heights, South Boston, Boston, Suffolk County, Massachusetts, 02127, United States. This is a on-site role.

Work location

Work model: On-site

location_on

143, Bolton Street, Dorchester Heights, South Boston, Boston, Suffolk County, Massachusetts, 02127, United States

Boston, Massachusetts

Key Responsibilities

  • check_circleEnsure Sponsor-Investigator and study teams adhere to FDA regulations and ICH/GCP guidelines
  • check_circleMonitor clinical trial progress through remote data review and onsite visits
  • check_circleProvide guidance to monitoring teams and assist in audit readiness preparation
  • check_circleAssist in training and orienting newly hired Clinical Trials Monitors
  • check_circleMentor monitoring team and conduct co-monitoring or training visits
  • check_circleVerify trial data consistency with patient clinical notes and source documentation
  • check_circleCoordinate monitoring assignments and submit written monitoring reports within timelines
  • check_circleAssist in developing and writing clinical trial monitoring plans

Requirements

  • verifiedBachelor's degree in a field related to research compliance
  • verified5 years of clinical trials experience
  • verified3+ years of monitoring experience
  • verifiedKnowledge of federal, state and local regulations
  • verifiedExperience interpreting legislation, regulations, policies, procedures, and ethical principles
  • verifiedAbility to translate regulations into operational policies and procedures
  • verifiedExpertise in research ethics and responsible conduct of research
  • verifiedComputer literacy in Microsoft Office suites (Word, Excel, PowerPoint)
  • verifiedWillingness and ability to travel occasionally

Nice to Have

Experience in academic institutions, particularly in collaborative roles with administrators, faculty, and research staff.

Dana-Farber Cancer Institute cover image
Dana-Farber Cancer Institute logo
Company

Dana-Farber Cancer Institute

Industry

Hospitals and Health Care

Headquarters

Boston, MA

Open Roles

1

Dana-Farber Cancer Institute operates within the hospitals and health care sector, based in Boston, MA. The organization focuses on delivering expert and compassionate medical services to children and adults diagnosed with cancer. Its core mission involves advancing the scientific understanding of cancer and related diseases, while simultaneously working to improve treatment protocols and strive for cures and prevention strategies. The institute serves a broad patient demographic across the region, integrating clinical care with research initiatives to address the complex challenges of oncology. By maintaining a dedicated approach to patient support and medical innovation, Dana-Farber Cancer Institute remains a significant entity in the field of health care.
View company profilearrow_forwardlanguageWebsitelinkLinkedIn
Quick Overview

Experience

5+ yrs (Senior)

Education

Bachelor's degree in a field related to research compliance required

Job Type

Full-Time

Skills Required

Good Clinical PracticeIch/gcpFda RegulationsSource Data VerificationMicrosoft OfficeWord
arrow_forward
Is this Clinical Trial Monitor II job remote, hybrid, or on-site?expand_more
Dana-Farber Cancer Institute has listed this Clinical Trial Monitor II role as on-site.
How much experience is required for this Clinical Trial Monitor II role?expand_more
Clinical Trial Monitor II at Dana-Farber Cancer Institute typically requires 5+ years of relevant experience at the senior level.
What skills do you need for the Clinical Trial Monitor II role at Dana-Farber Cancer Institute?expand_more
Key skills for Clinical Trial Monitor II at Dana-Farber Cancer Institute include Good Clinical Practice; Ich/gcp; Fda Regulations; Source Data Verification; Microsoft Office; Word; Excel; and Powerpoint.
What education is required for Clinical Trial Monitor II at Dana-Farber Cancer Institute?expand_more
Educational requirements for this role: Bachelor's degree in a field related to research compliance required.
What category does the Clinical Trial Monitor II role belong to?expand_more
Clinical Trial Monitor II at Dana-Farber Cancer Institute is part of the scientific & qa job category on Recrutus.

About Dana-Farber Cancer Institute

Dana-Farber Cancer Institute operates within the hospitals and health care sector, based in Boston, MA. The organization focuses on delivering expert and compassionate medical services to children and adults diagnosed with cancer. Its core mission involves advancing the scientific understanding of cancer and related diseases, while simultaneously working to improve treatment protocols and strive for cures and prevention strategies. The institute serves a broad patient demographic across the region, integrating clinical care with research initiatives to address the complex challenges of oncology. By maintaining a dedicated approach to patient support and medical innovation, Dana-Farber Cancer Institute remains a significant entity in the field of health care.

Browse more roles: All Dana-Farber Cancer Institute jobs, scientific & qa jobs on Recrutus.

Recrutus

Curating the world's most innovative career opportunities. We bridge the gap between visionary talent and industry-leading companies.

Search roles by city, category, skill, or job type — explore verified employers, salary benchmarks, and remote-friendly teams across India and beyond.

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Recrutus helps candidates discover roles that match their skills and helps teams reach qualified applicants faster. Browse by metro, discipline, or work style — from internships to senior leadership.

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