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Research Data Specialist II - Clinical Trials Office

Job Description

Job ID:
39960

Location:
10 Brookline Place West, Brookline, MA 02445

Category:
Clinical Research

Employment Type:
Full time

Work Location:
Hybrid: 2-3 days onsite/week

Overview

The CTO Research Data Specialist II will be assigned to work on data entry projects and will provide data entry services across all clinical research programs in the areas of data collection, computing, and database organization. Duties include the examination, synthesis, and evaluation of medical records; the abstraction and recording of pertinent medical information; and the monitoring of patient status. The Clinical Data Specialist will be responsible for the collection, management, and quality assurance review of patient clinical data. This is a hybrid position, on site 2-3 days per week.  

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, we educate tomorrow's physician/researchers, and we work with amazing partners, including other Harvard Medical School-affiliated hospitals.

Responsibilities

  • PRIMARY DUTIES AND RESPONSIBILITIES FOR CTO Research Data Specialist potition:  
    • Will be assigned / deployed to work on data entry projects as needed and prioritized by the CTO. 
    • Reviewing and abstracting the medical records for patients. Entering the clinical data into the Clinical Research Information Systems (CRIS).
    • Accessing patient demographic and clinical information from the clinical systems. Entering information into the database.
    • Support the clinical programs with outcomes data collection, reporting, analysis and audits
    • Ensures timely reporting to internal and external outcomes data repositories, including national repositories when required by regulatory requirements and U.S. law
    • Ensure case management documentation in patient medical records and other information management systems as assigned to support clinical program clinical care
    • Perform QA and QC procedures to ensure optimal data reporting as assigned
    • Develop knowledge of specialized data sources specific to outcomes data reporting, including routine reaching out to offsite providers to obtain information from medical records at outside sites of care.

SUPERVISORY RESPONSIBILITIES:

Assists in orienting and training of new staff, no direct reports

Qualifications

  • Bachelor’s Degree required. Master’s preferred. 1-3 years of clinical research experience in a health related field. Computer skills, including proficiency in the use of Microsoft Office products, required. Performs primary duties above independently and has progressed to performing more advanced skill sets as directed. Requires limited supervision. Experience working in a medical or scientific research setting or comparable technology orientated business environment required.

COMPETENCIES:

  • Demonstrates an understanding of the data elements within the assigned data repository
  • Ability to create and run appropriate reports from the data repository
  • Demonstrates an understanding of the consent process and can independently facilitate the consenting of subjects
  • Knowledgeable in data abstraction
  • Demonstrates the understanding of tissue banking regulation
  • Demonstrates an understanding of clinical research

KNOWLEDGE, SKILLS, AND ABILITIES REQUIRED:

  • Excellent organizational and communication skills required.
  • Strong interpersonal skills – ability to effectively interact with all levels of staff and external contacts.
  • Must be detail oriented and have the ability to follow-through.
  • Ability to effectively manage time and prioritize workload.
  • Must practice discretion and adhere to institutional confidentiality guidelines at all times.
  • Must have computer skills including the use of Microsoft Office.

At Dana-Farber Cancer Institute, 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 equally committed to diversifying our faculty and staff. Cancer knows no boundaries and when it comes to hiring the most dedicated and diverse professionals, neither do we. If working in this kind of organization inspires you, we encourage you to apply.

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.

EEOC Poster

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