Job Description

PLEASE NOTE: Must be authorized to work lawfully in the United States for any employer without sponsorship.

Kelly® Science & Clinical is seeking a Clinical Research Analyst for a temporary position (with potential to extend/covert) at a leading client in Kansas City, MO. If you’re passionate about bringing the latest scientific discoveries to life and are ready to take the next step in your career, trust The Experts at Hiring Experts.

Pay Rate:

$30-38.00/Hour (commensurate with experience)

Overview:

A Clinical Research Analyst plays a critical role in the identification of qualified clinical study participants and in the collection of data required to support the development of new diagnostic and screening solutions and other medical treatments and therapies. This position requires attention to detail, a commitment to ethical research practices, and a strong ability to work in a collaborative, interdisciplinary environment.

Schedule:

Friday – Monday, 1st/Day: Standard Hours

Responsibilities:

Study Planning:

• Collaborate with research teams to design and develop processes to meet the requirements of research protocols.

• Assist in selection of study participants, data collection methods, and study timelines.

Data Collection & Management:

• Oversee data collection for clinical studies, ensuring accuracy and regulatory compliance.

• Maintain and organize study-related documents and records.

• Review potential participants' clinical records to ensure study qualification.

• Ensure proper data entry within operational platforms (e.g., Electronic Data Capture System, Customer Relationship Management System).

Data Analysis:

• Utilize statistical and data analysis tools to process and analyze clinical data.

• Extract meaningful insights and trends to support research objectives.

Regulatory Compliance:

• Ensure all research activities adhere to ethical and regulatory guidelines (e.g., Good Clinical Practice, Institutional Review Board protocols).

• Stay updated on and strictly follow data privacy regulations (e.g., HIPAA, GDPR) and ensure compliance.

Reporting:

• Prepare comprehensive reports and summaries of research findings.

• Contribute to scientific publications and presentations.

Collaboration:

• Work with cross-functional teams to facilitate smooth execution of clinical studies.

Quality Control:

• Implement quality control measures to guarantee data accuracy and integrity.

• Identify discrepancies and address issues promptly.

Literature Review:

• Stay updated on current research trends and developments in clinical research.

Technology Utilization:

• Proficiently use data management software and statistical analysis tools.

Communication:

• Effectively communicate research progress, challenges, and findings to stakeholders.

Data Privacy & Security:

• Implement and maintain data privacy and security protocols.

• Conduct regular risk assessments and participate in security audits.

• Ensure proper data encryption and access controls are in place.

• Report any potential data breaches or security incidents immediately.

Qualifications:

• Bachelor's degree in a relevant field (e.g., Life Sciences, Statistics, Public Health).

• Strong analytical and data management skills.

• Excellent communication and collaboration skills.

• Detail-oriented with a focus on data accuracy and quality.

• Familiarity with ethical and regulatory guidelines in clinical research.

• Understanding of data privacy laws and information security best practices.

• Experience with clinical trial management systems and statistical software (e.g., SAS, R, SPSS).

• Certification in Good Clinical Practice (GCP) preferred.

Physical Requirements

• Ability to sit for extended periods and use a computer for long hours.

• May require occasional travel to research sites or conferences.

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