Clinical Data Coordinator (Remote) Apply Now

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🏢 Hiring.zycto📍 Longfellow, Minneapolis💼 Full-Time💻 Remote🏭 Biotechnology, Clinical Research, Pharmaceuticals💰 65,000 - 85,000 per year

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Seeking to redefine clinical research, Hiring.zycto stands at the forefront of innovation, empowering breakthroughs in patient care. For a Clinical Data Coordinator, our dynamic environment offers unparalleled opportunities to contribute meaningfully from anywhere, leveraging cutting-edge technology to streamline data management. We pride ourselves on a culture of precision, collaboration, and continuous learning, ensuring that every team member feels valued and impactful. Join us in shaping the future of medicine, where your expertise directly translates into tangible health outcomes.

Job Description

Hiring.zycto is actively seeking a highly meticulous and experienced Clinical Data Coordinator to join our fully remote team. This is an exceptional opportunity for a detail-oriented professional to play a pivotal role in the integrity and quality of clinical trial data, contributing directly to the advancement of medical science from the comfort of your home office. As a Clinical Data Coordinator, you will be instrumental in the end-to-end data management lifecycle, ensuring accuracy, completeness, and adherence to regulatory standards across various clinical studies. Your expertise will be vital in developing and maintaining databases, performing data review and query resolution, and generating reports that support critical decision-making processes.

This role demands a strong understanding of clinical research principles, Good Clinical Practice (GCP), and regulatory requirements. You will collaborate closely with study teams, investigators, and other data management professionals to ensure timely and high-quality data delivery. The ideal candidate will possess excellent analytical skills, a proactive approach to problem-solving, and the ability to thrive in a fast-paced, remote work environment. We are committed to fostering a supportive and collaborative atmosphere, even across distances, providing you with the tools and resources needed to excel. If you are passionate about data integrity in clinical research and eager to make a significant impact on global health initiatives, we encourage you to apply and become a key contributor to our innovative team at Hiring.zycto.

Your contributions will directly influence the success of our clinical trials, helping bring life-changing treatments to patients worldwide. This position offers not just a job, but a chance to be part of a mission-driven organization where your skills are truly valued.

Key Responsibilities

  • Develop, review, and maintain Case Report Forms (CRFs) and Electronic Data Capture (EDC) systems.
  • Perform extensive data review, validation, and query generation/resolution to ensure data quality and integrity.
  • Assist in the development and review of Data Management Plans (DMPs) and other study-specific documentation.
  • Conduct reconciliation of clinical data with external data sources (e.g., lab data, adverse events).
  • Participate in User Acceptance Testing (UAT) for EDC systems and database upgrades.
  • Generate data listings, reports, and summaries for internal review and regulatory submissions.
  • Ensure compliance with Good Clinical Practice (GCP), standard operating procedures (SOPs), and regulatory guidelines.

Required Skills

  • Proficiency in Electronic Data Capture (EDC) systems (e.g., Medidata Rave, Oracle Clinical).
  • Strong understanding of clinical research principles and regulatory requirements (GCP, ICH guidelines).
  • Excellent attention to detail and analytical problem-solving skills.
  • Demonstrated ability to manage multiple projects and priorities effectively in a remote setting.
  • Proficiency in Microsoft Office Suite (Excel, Word, PowerPoint).
  • Exceptional verbal and written communication skills.
  • Ability to work independently and as part of a virtual team.

Preferred Qualifications

  • Bachelor's degree in a life science, health informatics, or a related field.
  • Certification in Clinical Data Management (e.g., CCDM).
  • Experience with SAS or SQL for data manipulation and reporting.
  • Familiarity with medical coding dictionaries (e.g., MedDRA, WHODrug).

Perks & Benefits

  • Fully remote work model with flexible hours.
  • Comprehensive health, dental, and vision insurance.
  • Generous paid time off and holidays.
  • 401(k) matching program.
  • Opportunities for professional development and continuous learning.
  • Home office stipend and technology support.
  • Collaborative and supportive virtual team environment.

How to Apply

Eager to contribute to cutting-edge clinical research from a remote setting? We invite you to apply by clicking on the application link below. Please ensure your resume highlights your relevant experience in clinical data management. We look forward to reviewing your application and potentially welcoming you to the Hiring.zycto team!

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