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 Centralized Study Associate II to join our team at Yeswanthpura in Bangalore, Karnataka.

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. 

Minimum Qualifications
• Bachelor's degree in science

Preferred Qualifications
• Master's degree in science.

Additional Job Standards

• The Labcorp Competencies define the behaviors necessary for the organization to achieve business outcomes.  Please refer to the Covance Competencies for more information about company-wide expectations for all employees.

• Problem Solving/Logic Skills.

• Strong communication and interpersonal skills.

• Working knowledge of SQL

• Strong MS/Office skills, particularly with Excel and Word.

• Knowledge of informed consent forms essential.

• Experience writing, reviewing, or reading informed consent for clinical trials.

• Knowledge of global regulation and guidance documents in relation to informed consent information.

• Strong drive for process optimization and data integrity.

• Experience with 21 CFR Part 11 in a pharmaceutical, biotechnology, CRO, or related industry.

• Excellent communication and interpersonal skills with great attention to detail.

• Problem-solving/Logic Skills

Labcorp is proud to be an Equal Opportunity Employer:

Labcorp strives for inclusion and belonging in the workforce and does not tolerate harassment or discrimination of any kind. We make employment decisions based on the needs of our business and the qualifications and merit of the individual. Qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, sex (including pregnancy, childbirth, or related medical conditions), family or parental status, marital, civil union or domestic partnership status, sexual orientation, gender identity, gender expression, personal appearance, age, veteran status, disability, genetic information, or any other legally protected characteristic. Additionally, all qualified applicants with arrest or conviction records will be considered for employment in accordance with applicable law. 

We encourage all to apply

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