Freshers Clinical Research Job Vacancies at Labcorp
Informed Consent Codification Associate
locations: Bangalore India
time type: Full time
posted on: Today
time left to apply: End Date: August 21, 2025 (11 hours left to apply)
job requisition id: 2519035
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 identifying errors and resolution steps.
- Triages unacceptable errors for resolution
- Maintains and utilizes a strong knowledge of SOPS and validation work procedures/ standards concerning the System Development Life Cycle.
Metrics
Support management of metrics.
Assist with investigating or resolving issues of quality as directed.
Process Improvement
Suggest process improvements where issues are seen.
Support Six Sigma process improvement teams.
Training / SOPs
Mentor and support other employees in understanding and adopting Informed consent codification.
Other
Lead or assist with special projects as designated.
Perform other duties as assigned by management.
Minimum Education and Experience Required:
- University/College Degree, preferably in the sciences or a related field.
- 0-1 year of experience working in clinical trials, laboratory, or specimen management
- Knowledge of informed consent forms is essential
- Experience writing, reviewing, or reading informed consent for clinical trials
- Knowledge of global regulations and guidance documents concerning informed consent information.
Skills and Competencies:
- Excellent communication and interpersonal skills with great attention to detail
- Strong MS/Office skills, with Excel and Word.
- Problem-solving/Logic Skills
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