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Clinical Dynamix

16 Clinical Dynamix Jobs Hiring Near You

Clinical Dynamix

Chief Medical Officer

Jersey City, NJ · On-site

Key Responsibilities Areas of specific responsibility and attention will include the following: • Provide leadership and clinical perspective to the research, development, quality and comprehensive ...

Clinical Dynamix

Executive Assistant

Hauppauge, NY · On-site

Executive Assistant to the Founder Location: Hauppauge, NY (In-Office) Position Overview Company is seeking a highly organized and proactive Executive Assistant (EA) to provide full-time, in-office ...

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Clinical Dynamix Jobs Information

Infographic showing various job openings at Clinical Dynamix in the United States as of May 2026, with employment types broken down into 100% Full Time. Highlights an 91% Physical, and 9% Hybrid job distribution.

Clinical Trials Manager

Clinical Dynamix

Burlington, MA • Hybrid

Full-time

This job post has expired 1 day ago. Applications are no longer accepted.

Job description

Position Summary (Hybrid; 2-3 days in office)
The Clinical Trials Manager is responsible for the delivery of a key phase 3 clinical trial. This individual will contribute to the success of the team and organization by delivering high quality operational excellence on all delegated responsibilities while upholding our core working behaviors of Trust and Respect, Communication and Feedback, Accountability and Reliability, Objectivity, and Team Balance and Enablement.
Key Responsibilities

  • Provide strategic and operational oversight for global clinical trials.
  • Support CRO and vendor management, including governance, performance tracking, and risk mitigation.
  • Collaborate with internal functions (Regulatory, Medical, Biometrics, Pharmacovigilance, CMC, quality) to align on study plans and timelines.
  • Monitor trial progress against key deliverables (recruitment, data quality, protocol compliance, etc).
  • Review, drive essential trial documents (protocols, ICFs, plans, manuals).
  • Support country and site selection, start-up activities, and site engagement strategy.
  • Manage and support sites in study maintenance for a fast-enrolling trial
  • Ensure compliance with ICH-GCP, SOPs, and applicable regulatory requirements.
  • Support study budgets and contracts in collaboration with finance and legal teams.
  • Contribute to clinical development strategy and operational planning.
  • Prepare for and participate in study audits, inspections and data deliverables
  • Attend Site Investigator Visits and build and maintain relationships with key stakeholders.
  • Adhering to Company Standard Operating Procedures, Policies and applicable regulatory requirements
  • Execute day-to-day responsibilities of the role, ensuring quality, accuracy, and timeliness.
  • Collaborate effectively with colleagues, sharing knowledge and supporting team goals.
  • Contribute to problem-solving and decision-making processes with an objective, data-driven approach.
  • Communicate clearly and proactively with stakeholders to ensure alignment.
  • Demonstrate ownership of tasks and follow through to successful completion.
  • Support team members through constructive feedback, mentorship, and collaboration.
Skills and Qualifications
  • Bachelor's degree in life sciences, nursing, pharmacy, public health, or a related field (Advanced degree preferred but not required)
  • ~7 years in Clinical Operations or related function
  • Strong working knowledge of ICH-GCP, and experience working on global clinical trials
  • Strong interpersonal and communication skills, with the ability to adapt to different audiences.
  • Excellent organizational skills
  • Proven ability to build trust and credibility through integrity, openness, and respect.
  • Demonstrated accountability in delivering results and meeting commitments.
  • Analytical mindset with the ability to use facts and data to guide decisions.
  • Ability to work both independently and collaboratively within a team.

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