Clinical Project Manager- Point of Care

Job Summary

The Project Lead is responsible for ensuring that all studies are designed planned executed monitored closed out and documented in an appropriate manner within the planned timeframe and cost; ensuring that the sponsor responsibilities are fulfilled while assuring compliance to all applicable regulatory requirements. Responsible for the timeline and budget planning and execution of studies. Assigns and ensures delivery of specific tasks to / from other members of the study team. Provides oversight to outside support including CROs consultants and / or medical advisors.

Responsibilities

Leading the global study team with full accountability for study deliverables regarding quality budget and timelines.

Developing key study documents (e.g. Design Validation Plan protocol study training materials study forms and templates study report).

Overseeing planning and operational aspects of companion diagnostics studies sponsored by Pharma partners.

Ensuring adherence to regulations guidelines and standard operating procedures and ensuring audit / inspection readiness.

Executing sponsored studies for assigned areas of focus through all study phases (planning start-up conduct and close-out).

Overseeing projects to ensure completion on-time within scope and budget; tracking project performance to analyze the completion of short and long-term goals.

Building and maintaining strong collaborative relationships with cross-functional leaders key internal and external stakeholders and other alliance partners including CROs.

Collaborating across Clinical Operations and other functions to develop and implementing best practices across Clinical Operations.

Requirements

Experience in clinical performance studies and analytical performance studies in point of care field

Experience in Emergency Department studies and CRO oversight experience

Understanding of precision and reproducibility studies in POC settings

Team-oriented with excellent collaboration skills with a cross-functional team.

Open-minded to learn new ways of doing things while leveraging previous experience.

Minimum of a bachelors degree in Life Science and / or relevant expertise in the Healthcare Industry or a related field at least 5years of prior relevant experience including >

1 years project management experience.

Conceptual and practical knowledge of Product Development and basic knowledge of Clinical Operations or related areas.

IQVIA is a leading global provider of clinical research services commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide . Learn more at

IQVIA is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race color religion sex sexual orientation gender identity national origin disability status as a protected veteran or any other status protected by applicable law. potential base pay range for this role when annualized is $93100.00 - $232800.00. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge skills education and experience; location; and / or schedule (full or part-time). Dependent on the position offered incentive plans bonuses and / or other forms of compensation may be offered in addition to a range of health and welfare and / or other benefits.

Required Experience :

IC

Key Skills

Corporate Paralegal,Car Driving,Design Engineering,Electrical Controls,Consultancy

Employment Type : Full-Time

Experience : years

Vacancy : 1

Monthly Salary Salary : 93100 - 232800