Central Clinical Data Coordinator I

2 weeks ago

Karachi, Sindh, Pakistan DM CLINICAL RESEARCH GROUP Full time 1,200,000 - 2,400,000 per year

Job Details
Job Location:    Corporate - Karachi (KHI) - Karachi, Sindh
Salary Range:    Undisclosed

Central Clinical Data Coordinator I

The Central Clinical Data Coordinator I works to coordinate and implement data collection for various studies, focusing on the day-to-day operations.

DUTIES & RESPONSIBILITIES

  • Transcribe and manage data for assigned clinical studies
  • Maintain training & working knowledge of current FDA GCP/ICH guidelines, organizational SOPs, guidance documents, work instructions, and study protocols.
  • Ensure the quality and timeliness of data transcribed for assigned studies within appropriate reporting requirements
  • Contribute towards ensuring internal processes are in accordance with study requirements
  • Resolve any discrepancies, queries and other study-related abnormalities in-line with company and study protocols
  • Complete eDiary functions
  • Adequately document and report on clinical trial progress as per applicable requirements
  • Participate in required trainings as set forth by the company, department, sponsors, and trials
  • Participate in trainings and meetings as required
  • Perform quality checks as required by Clinical Data management
  • Any other matters as assigned by management pertinent to trial related functions.

KNOWLEDGE & EXPERIENCE

Education:

  • High school diploma required, Associate degree or Bachelor's preferred

Experience:

  • Experience with medical terminology is a plus
  • Experience with data entry is a plus

Credentials:

  • N/A

Knowledge and Skills:

  • Strong knowledge of Google Suite products, Clinical Databases and other computer-related software
  • Excellent oral and written communication skills
  • Excellent planning and organizational skills with effective time management
  • Excellent interpersonal skills
  • Meticulous, independent, and capable of working with minimal supervision
  • Excellent data handling and analysis
  • Problem-solving skills
  • Thorough understanding of clinical research principles and processes. Ability to input into process
  • initiatives, and procedures related to Good Clinical Practices (GCP).
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