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Clinical Research Coordinator - Multiple Myeloma

7 days ago

Pay$48100.00 - $54400.00 / year
LocationBoston/Massachusetts
Employment typeFull-Time
  • Job Description

      Req#: JR-2267
      Employer Industry: Healthcare - Cancer Research

      Why consider this job opportunity:
      - Salary up to $54,400
      - Opportunity for career advancement and growth within the organization
      - Work in a mission-driven environment focused on conquering cancer and improving patient care
      - Supportive and inclusive workplace culture that values diversity
      - Chance to contribute to groundbreaking cancer research and clinical trials
      - Engage directly with patients and make a positive impact on their lives

      What to Expect (Job Responsibilities):
      - Oversee the clinical trials start-up process, including protocol receipt and IRB submissions
      - Manage data reporting and collection of source documents, including adverse event reporting
      - Ensure compliance with study protocols and regulatory requirements for sample collection and shipping
      - Coordinate and prepare for internal and external audits and study monitoring visits
      - Interact with study participants and maintain accurate data entry in the Clinical Trial Management System

      What is Required (Qualifications):
      - Bachelor's Degree or 1 year of experience as a Dana-Farber Associate Clinical Research Coordinator
      - 0-1 years of experience in a medical or scientific research setting or comparable technology-oriented business environment
      - Excellent organization and communication skills
      - Strong interpersonal skills with the ability to interact effectively with all levels of staff and external contacts
      - Proficiency in Microsoft Office and strong attention to detail

      How to Stand Out (Preferred Qualifications):
      - Experience working in a clinical research setting or with clinical trials
      - Knowledge of Good Clinical Practice (GCP) guidelines
      - Familiarity with clinical trial management systems
      - Ability to manage time effectively and prioritize workload
      - Understanding of regulatory compliance and IRB processes

      #CancerResearch #ClinicalTrials #HealthcareCareers #PatientCare #DiversityAndInclusion

      "We prioritize candidate privacy and champion equal-opportunity employment. Central to our mission is our partnership with companies that share this commitment. We aim to foster a fair, transparent, and secure hiring environment for all. If you encounter any employer not adhering to these principles, please bring it to our attention immediately. We are not the EOR (Employer of Record) for this position. Our role in this specific opportunity is to connect outstanding candidates with a top-tier employer."
  • About the company

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