Informed Consent Codification Associate
About the Role
Company Description
Labcorp is a company working in the field of life sciences. They use scientific research, lab skills, data and new technology to help people make choices about their health. The work at Labcorp involves testing for diseases, helping to create drugs and performing clinical research. Labcorp supports doctors, researchers, drug companies and patients. Because Labcorp has many scientific tools and works in many different countries, Labcorp helps move medical science forward and helps patients get well.
Job Summary
The Informed Consent Codification Associate helps with trial tasks by sorting and coding informed consent info for different projects. This job requires you to look at consent papers closely. You must finish the Informed Consent Codification Associate work on time every day. You need to find any mistakes that must be reported. You also have to follow all the rules and ways of working. The Informed Consent Codification Associate helps keep data clean, finds ways to make things better and solves problems to get the job done right.
Key Responsibilities
Do informed consent coding tasks for client projects.
Make sure all informed consent coding work is done correctly and on time.
Look at all the information carefully to find mistakes or things that do not match.
Look into problems. Figure out how to fix them.
Tell the team if you find errors.
Follow all the rules and work practices.
Help watch how well the team is doing with their goals.
Help fix quality problems.
Find ways to make the current work steps better and faster.
Help with Six Sigma or other ways to keep improving when asked.
Help your teammates by sharing what you know about coding.
Help with projects and other tasks you are given.
Educational Qualification
A Bachelor’s degree in Science or a related discipline.
Having a Master’s degree in Science is a plus.
It is important to know about the consent papers used in research.
Skills Required
Understanding of informed-consent forms and clinical-trial documentation.
Able to read info and keep data at a high quality.
Good logical and troubleshooting skills.
Must have an eye for small details and accuracy.
Should know the rules about consent.
Understand SOPs, validation procedures and SDLC practices.
Good at using Microsoft Word and Excel.
Knowing how to use SQL is a bonus for this job.
Knowledge of 21 CFR Part 11 is a plus.
Salary Structure
The starting salary for an Informed Consent Codification Associate at Labcorp in India typically ranges from ₹5.2 LPA to ₹7.1 LPA.
Career Development
This job can help you learn a lot, about clinical-trial documentation, informed-consent processes, data quality, rules and how clinical research works.
With experience, you can move up into roles like Clinical operations, study management, clinical data management, regulatory compliance, or senior clinical research positions.
How to Apply
Go to our career portal. Look for the Informed Consent Codification Associate job.
Open the job page. Check the eligibility criteria for the job.
Click Apply. Fill out your profile with all the info.
Upload your resume, check everything one time, and send your application.
Market Insights & Trends
Salary Insights
The amount of money that gets paid can be different depending on how they have been working, where they live and what kind of job they are doing. Some places pay more than others. Most good jobs include extra money for doing a good job, health insurance and flexible hours. Companies pay high salary to make sure they can get the people they want.
Hiring Trends
The number of jobs for this profile is going up every year. Hospitals and other healthcare companies are looking for people who're good, at their job and can also figure out new problems. They want who can do the work and also think on their feet to deal with the challenges of working in healthcare today.