Clinical Project Manager at Abbott Pediatrics

Alameda, California, United States -

Full Time

Start Date

Immediate

Expiry Date

16 Feb, 26

Salary

173300.0

Posted On

18 Nov, 25

Experience

5 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Clinical Study Management, Project Planning, Cross-Functional Collaboration, Operational Oversight, Standard Operating Procedures, Good Clinical Practice, Process Improvement, Mentoring, Communication Skills, Problem Solving, Regulatory Compliance, Training, Timeline Management, Team Coordination, Adaptability, Issue Resolution

Industry

Hospitals and Health Care

Description

Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 114,000 colleagues serve people in more than 160 countries. The Opportunity: We are searching for an individual contributor to join our Alameda, California team with comprehensive knowledge in specific areas. We need someone with the ability to execute highly complex or specialized projects. Someone who also adapts precedent and may make significant departures from traditional approaches to develop solutions. This individual will be assisting the manager in the leading & mentoring of the junior clinical staff. What you will do: Plans, directs, creates and communicates clinical study timelines. Gathers input from cross-functional teams and creates plans that help the team produce deliverables on schedule. Ensure consistency of clinical studies and processes across clinical trials. Oversees and resolves operational aspects of clinical trials in conjunction with project teams and in accordance with standard operating procedures (SOP), good clinical practice (GCP) and specific country regulations such as the approved release of investigational devices for clinical studies. Develop and refine SOPs for existing and new staff and training clinical sites on clinical procedures, when needed. Ensures study is conducted within clinical trial protocols. Monitors progress and follow up with team members and line managers when issues develop. Identify and participate in process improvement initiatives. May participate in a lead role for a project Qualification Requirements: Associate’s degree with a minimum of 5-7 years of industry experience; bachelor's degree preferred. Must be able to travel up to 25%-30%. Strong communication and written skills. The base pay for this position is $86,700.00 – $173,300.00. In specific locations, the pay range may vary from the range posted.

How To Apply:

Incase you would like to apply to this job directly from the source, please click here

Responsibilities

The Clinical Project Manager plans, directs, and communicates clinical study timelines while ensuring consistency across clinical trials. They oversee operational aspects of clinical trials and participate in process improvement initiatives.