Senior Clinical Project Administrator

Senior Clinical Project Administrator

Labcorp is a global leader in diagnostic testing and drug development solutions, helping healthcare providers, researchers, and patients make informed decisions that advance care. Join us in our mission to improve health and improve lives.

Labcorp is seeking a Clinical Project Associate to join our team at Brigade Twin Tower in Bangalore, Karnataka .

Work Schedule

Rotating shift - 5 days working model

Job Responsibilities

Follow applicable departmental Standard Operating Procedures and Work Instructions.

 Complete required trainings according to required timelines.

 Manage day-to-day tasks ensuring quality and productivity.

 Manage project and technical documentation in an appropriate manner.

 Provide administrative and technical support to internal departments as needed.

 Perform checks to ensure quality of work completed.

 Ensure timely escalation and issue resolution.

 Track and report metrics as determined by management according to required timelines.

 Assist with the implementation of revised processes and procedures.

 Other additional duties as assigned by management but not limiting the ones to the ones listed below: Develop a deep understanding of an assigned job and provide solutions to solve specific problems using unique expertise in the subject.

 Guide and develop the mentee to acquire all competencies required to perform the daily tasks independently post sign-off as assigned by management.

 Active listening, showing patience and willingness to help at all times and being available for the mentee

 Ensure Training files for team are be maintained up to date and Audit ready all the times. Track Weekly/Monthly Training compliance of Team

 Actively participate and contribute in various Knowledge Sharing Session held across departments within CTTS.

 Appropriate Assessment of Workload and assigning the projects on time based on priority.

 Perform quality check of peers and Identify process gaps that lead to quality errors and suggest steps to improve quality compliance for assigned tasks.

 Plan and deliver training; Prepare required training agenda and material.

 To create and/or perform review by assessing effectiveness, update SOP's/WI's including timely submission of version controlled documents to global QA SOP team.

Minimum Qualifications

Bachelor's Degree in Science

Preferred Qualifications

3 years of experience working in a clinical research industry

Master's Degree in Science

Additional Job Standards

Demonstrated ability to plan, prioritize, organize and communicate effectively.

Demonstrated ability to pay attention to detail.

Strong interpersonal skills with ability to work well with others.

Ability to deliver consistent high quality of work.

Ability to use computer and departmental tools.

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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Experience Level

Senior Level