Labcorp is seeking a Informed Consent Codification Associate I to join our team in Bangalore, India.
Work Schedule
Monday - Friday - Rotating Shift
Job Responsibilities
Perform informed consent codification across multiple client instances.
Informed consent codification executed to completion correctly.
Delivery schedules are met.
Robust 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.
Minimum Qualifications
Bachelors degree in science
6 months of experience in writing, reviewing, or reading informed consent for clinical trials
Preferred Qualifications
Masters degree in science.
6 months of experience in programming languages and tools such as SQL and python
Additional Job Standards
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.
Solid communication and interpersonal skills.
Strong MS/Office skills, particularly with Excel and Word.
Knowledge of informed consent forms
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.
Solid drive for process optimization and data integrity.
Excellent communication and interpersonal skills with outstanding attention to detail.
Experience with 21 CFR Part 11 in a pharmaceutical, biotechnology, CRO, or related industry.
Disclaimer: This job posting has been aggregated from external source. Role details, content, and availability are subject to change. Applicants are advised to confirm the latest information directly on the company website before applying.