Informed Consent Codification Associate

Labcorp is a global leader in laboratory services, providing the insights and answers that help healthcare providers, patients, researchers, pharmaceutical companies and health systems make confident decisions and improve outcomes. Through our unparalleled science, data, technology and laboratory network, we advance diagnostics, accelerate innovation and help address some of the world's most important health challenges. As we shape the future of healthcare, we are leveraging advanced technologies, intelligent digital solutions and data-driven innovation across our operations to enhance how work gets done and deliver greater value to customers and patients. With our global scale and deep expertise, you'll have the opportunity to do meaningful work, grow your career and make a real impact on people's health around the world. Together, we're improving health and improving lives.

Labcorp is seeking a Informed Consent Codification Associate I to join our team at Brigade Twin Tower in Bangalore, India.

Work Schedule
Monday - Friday -Rotating Shift

Job Responsibilities

Function Specific

• Perform informed consent codification across multiple client instances.
• Informed consent codification executed to completion correctly
• Delivery schedules are met.
• Strong troubleshooting and analytical skills for the identification of errors and resolution steps.
• Triages unacceptable errors for resolution
• Maintains and utilizes a strong knowledge of SOPS and validation work procedures/standards in relation to the System Development Life Cycle.

• The Labcorp Competencies define the behaviors necessary for the organization to achieve business outcomes. Please refer to the Labcorp Competencies for more information about company-wide expectations for all employees.
• Problem Solving/Logic Skills.
• Strong communication and interpersonal skills.
• Strong MS/Office skills, particularly with Excel and Word.
• Knowledge of informed consent forms essentia Knowledge of global regulation and guidance documents in relation to informed consent information
• Proven ability to plan, prioritize, and manage in a fast-paced environment with a high degree of initiative.
• Strong drive for process optimization and data integrity.
• Excellent communication and interpersonal skills with great attention to detail.
• Experience with 21 CFR Part 11 in a pharmaceutical, biotechnology, CRO, or related industry.

Labcorp is transforming how patients are diagnosed, monitored, and treated.