Informed Consent Codification Associate

2 weeks ago

Bengaluru Karnataka, India Labcorp Full time

**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

**Labcorp is proud to be an Equal Opportunity Employer**:
**We encourage all to apply

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