Clinical data analyst

job summary: Join a high-energy Research and Innovation Lab dedicated to pioneering the next generation of skin biology and dermatological products. As a Clinical Data Analyst I, you will play a mission-critical role in the operational success of human clinical trials. You will serve as the primary link between clinical strategy and execution, overseeing the complex logistics of study products, instrumentation, and data integrity. This is an ideal role for a detail-oriented professional who thrives in a fast-paced laboratory environment and wants to ensure that every study-from eCRF monitoring to final reporting-meets the highest standards of scientific excellence and global compliance.

location: Clark, New Jersey job type: Contract salary: $40 - 45 per hour work hours: 9 to 5 education: Bachelors

responsibilities

• Clinical Operations & Logistics: Lead the end-to-end coordination of study materials, including the ordering, labeling, and shipping of study products to ensure all timelines are met.
• Instrument Management: Act as the primary custodian for the team's clinical instruments and hardware; maintain tracking logs and ensure all diagnostic tools are calibrated and ready for study use.
• Study Execution & Monitoring: Support Clinical Project Managers in the execution of skin biology studies, including e-monitoring of eCRF systems and the compilation of complex study results and imaging data.
• Quality Assurance (QA/QC): Serve as the team's Key Quality Person, performing rigorous QA/QC on study reports to ensure 100% compliance with global Quality guidelines and GDPR regulations.
• Stakeholder Collaboration: Maintain proactive, professional relationships with internal Data Management and Statistical teams, as well as external CROs and global Advanced Research partners.
• Independent Project Driving: Manage multiple operational workstreams independently, ensuring clinical study integrity is never compromised. qualifications: Required:
• Education: Bachelor's degree in a relevant scientific field (e.g., Biology, Chemistry, Public Health, or Life Sciences).
• Experience: 3-5 years of professional experience, with a minimum of 1 year specifically focused on managing and monitoring Human Clinical Trials (Pharma, OTC, or Personal Care).
• Regulatory Knowledge: Solid understanding of Good Clinical Practices (GCP) and FDA guidelines.
• Technical Literacy: Proficiency in eCRF systems and data compilation; experience working directly with CROs.
• Soft Skills: Exceptional communication and presentation skills with a proven ability to drive projects forward with minimal supervision. Preferred:
• Subject Matter Expertise: Strong foundational knowledge of Skin Biology or Dermatology.
• Technical Tools: Working knowledge of instrumental and clinical evaluation methods or diagnostic tools used to measure product efficacy.
• Compliance: Previous experience acting as a lead for Quality or GDPR compliance within a clinical setting. #LI-HK1

skills: Chemistry, Sample Preparation, Quality Management Systems (QMS)

Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status.

At Randstad, we welcome people of all abilities and want to ensure that our hiring and interview process meets the needs of all applicants. If you require a reasonable accommodation to make your application or interview experience a great one, please contact HRsupport@randstadusa.com.

Pay offered to a successful candidate will be based on several factors including the candidate's education, work experience, work location, specific job duties, certifications, etc. In addition, Randstad offers a comprehensive benefits package, including: medical, prescription, dental, vision, AD&D, and life insurance offerings, short-term disability, and a 401K plan (all benefits are based on eligibility).

This posting is open for thirty (30) days.