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Healthcare Data Analyst

Biofusion

Atlanta, Georgia, United States · Full Time

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Experience
1–5 yrs
Salary
Openings
1
Posted
1 तासपूर्वी
Work mode
In office
Education
Bachelor's degree
Resume
Required to apply

Where you'll work

Job description

Role Overview

This position supports clinical operations across multiple projects, focusing on operational strategy development, timeline monitoring, and collaboration with vendors to ensure smooth clinical trial processes.

Key Responsibilities

  • Support clinical operations in various projects by managing trial logistics, compliance, and data collection.
  • Assist in formulating and implementing operational strategies aligned with clinical trial goals.
  • Monitor project timelines and deliverables to meet preset milestones.
  • Collaborate with external vendors and cross-functional teams for streamlined trial execution.
  • Lead and manage clinical research projects, including protocol and budget development.
  • Ensure adherence to regulatory and ethical standards within clinical trials.
  • Mentor junior staff and coordinate communication between clinical teams and stakeholders.
  • Oversee clinical trial data management, ensuring accuracy, integrity, and regulatory compliance.
  • Coordinate patient recruitment and retention efforts to support trial success.

Educational Background and Experience

  • Bachelor's degree in Health Sciences, Life Sciences, Nursing, Computer Science, or related field is preferred.
  • Master's or PhD degrees in Clinical Research, Data Science, or related fields are relevant for advanced roles.
  • Relevant clinical experience varies from 1 to over 5 years depending on role specifics, with competencies ranging from clinical operations support to research management.

Required Skills and Competencies

  • Strong organizational, multitasking, and leadership abilities.
  • Excellent communication and interpersonal skills for effective team collaboration.
  • Proficiency with clinical trial processes, data management, and statistical software.
  • Knowledge of regulatory and ethical standards such as GCP and FDA guidelines.
  • Capacity to work independently and as part of multidisciplinary teams.

Additional Information

  • This role encompasses various levels of clinical operation tasks including trial coordination, data management, research project leadership, and compliance monitoring.
  • Candidates with strong problem-solving skills and experience in fast-paced clinical environments are encouraged to apply.

Work styles they’re looking for

Problem Solving Teamwork Attention to Detail Communication Skills Team Leadership Organizational Skills Independent Work
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