Clinical Data Specialist

Redbock - an NES Fircroft company; Minnesota; Remote; Full time

Job summary

An established industry player is seeking a Clinical Data Specialist for a 24-month remote contract. In this pivotal role, you will oversee the full life cycle of clinical data, ensuring its integrity and quality while collaborating with various departments. Your expertise in project management and data collection will be crucial in designing clinical protocols and optimizing data systems. This position offers a unique opportunity to work in a dynamic environment within the medical and pharmaceutical sectors, where your contributions will directly impact clinical outcomes. If you are passionate about data management and thrive in a team-oriented setting, this role is perfect for you.

Qualifications

• 2-4 years of Clinical Data Management experience required.
• Bachelor’s degree in Life Sciences or Computer Science is essential.

Responsibilities

• Manage the life cycle of clinical data from collection to delivery.
• Ensure data integrity and quality for clinical studies.

Skills

Project Management

Data Collection Definition

Data Quality Management

Data Continuity and Optimization

Education

Bachelor’s Degree in Life Sciences

Bachelor’s Degree in Computer Science

Job description

Redbock - an NES Fircroft company provided pay range

This range is provided by Redbock - an NES Fircroft company. Your actual pay will be based on your skills and experience — talk with your recruiter to learn more.

Base pay range

$30.00/hr - $35.00/hr

*W2 ONLY*

Clinical Data Specialist (24 month contract // REMOTE, team based in MN):

HM's Top 4:

• Project Management
• Data Collection Definition
• Data Quality Management
• Data Continuity and Optimization

Education Required: Bachelor’s Degree in Life sciences or Computer Science

Years’ Experience Required: 2-4 years of Clinical Data Management experience

Description:

The Clinical Data Specialist position is responsible for the life cycle of clinical data from collection to delivery for analysis. This includes ensuring the necessary data is being collected to meet study goals and achieving both data integrity (i.e., data is managed the right way) and data quality (i.e., data is credible and reliable).

Duties:

• This position requires the ability to demonstrate strong functional leadership over time through:
• Delivering on commitments
• Incorporating Quality by Design
• Developing and maintaining strong partnerships
• Staying current with industry trends through continuous learning
• Acting as a data privacy steward
• Applying risk-based decision making
• Collaborates with various departments on the design, documentation, testing, and implementation of clinical data collection studies, and clinical database review.
• Design and implement clinical protocols and data collection systems.
• Develops systems for organizing data to analyze, identify and report data and trends.
• Manages data management issues by reviewing protocols for cross-project consistency and identifying standard Case Report Form (CRF) modules to meet objectives.
• Provide early strategic input into protocol design focused on data management issues.
• Review and resolve data discrepancies for standardized data validation systems and procedures.
• Prepares reports of clinical trial studies for internal validation and cross validation studies.

Seniority level

Mid-Senior level

Employment type

Contract

Job function

Analyst, Quality Assurance, and Project Management

Industries

Medical Equipment Manufacturing, Pharmaceutical Manufacturing, and Biotechnology Research