Job Description

Job Description

Job Description

We are looking for a Clinical Data Entry Clerk for a Medical Device company. The opportunity is for 40 hours a week with potential for growth. This position could become a permanent position. The perfect candidate will have the following skill sets:

A Clinical Trial Data Entry Coordinator position involves accurately entering and managing clinical trial data into electronic systems, ensuring data quality and compliance with study protocols. Responsibilities include data entry, verification, query resolution, and supporting data management aspects of clinical trials. Strong attention to detail, organizational skills, and knowledge of electronic data capture Microsoft Access is essential . 

Key Responsibilities:

• Data Entry and Management:

  Accurately entering clinical trial data from source documents into electronic databases and ensuring timely updates. 

• Data Verification and Quality Control:

  Verifying data for consistency, identifying and resolving discrepancies, and ensuring data accuracy. 

• Query Resolution:

  Responding to data queries from the clinical team and other stakeholders, and ensuring timely resolution of issues. 

• Database Management:

  Assisting with database management tasks, including data entry, cleaning, and preparation for analysis. 

• Compliance and Reporting:

  Ensuring data integrity and compliance with study protocols, regulations, and standard operating procedures (SOPs). 

• Collaboration:

  Working closely with clinical research coordinators, investigators, and other team members to ensure data quality and completeness. 

• Study Support:

  Providing general support to the clinical research team, including preparing reports, assisting with data audits, and supporting data queries. 

Essential Skills and Qualifications:

• Strong Attention to Detail: Meticulousness in data entry and verification. 
• Excellent Organizational Skills: Ability to manage data and prioritize tasks effectively. 
• Understanding of Medical Terminology: Familiarity with medical terms and concepts. 
• Proficiency in Electronic Data Capture using Access . 
• Strong Communication Skills: Ability to communicate effectively with team members and stakeholders. 
• Time Management Skills: Ability to meet deadlines and manage workload efficiently. 
• Knowledge of Clinical Trial Processes: Understanding of the clinical trial lifecycle and relevant regulations. 

Education and Experience:

• A bachelor's degree in a relevant field (e.g., life sciences, health sciences, or a related area) is often preferred, though some positions may accept equivalent experience. 
• Previous experience in clinical research, particularly in data management, is nice to have but not required. 
• Experience with Microsoft Access is a requirement.

We are a specialized Global staffing firm that works for Fortune 500 companies in the Medical Device, Pharmaceutical, and Biotec industries, finding qualified personnel.

Company Description

We are a specialized Global staffing firm that works for Fortune 500 companies in the Medical Device, Pharmaceutical, and Biotec industries, finding qualified personnel.

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