job title: Informed consent codification associate(labcorp)

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