Senior Project Manager - Med Device

Elite Talent Partners; California (MO); Hybrid; USD 90,000 - 120,000; Full time

Job summary

A leading medical device consulting firm is seeking an experienced Senior Project Manager to oversee cross-functional projects in the cardiac space. This role requires at least 4 years in medical device or pharma clinical research, with a focus on managing cardiovascular device trials. The ideal candidate will possess strong project management skills, regulatory knowledge, and a relevant degree. This contract position involves travel to various states, including North Carolina and Minnesota.

Qualifications

• At least 4 years' experience in medical device/pharma clinical research industry required.
• At least 2 years' project management experience.
• At least 1 year experience in a managerial role.

Responsibilities

• Planning and implementation of cross-functional projects within medical device.
• Define project tasks and resource requirements.
• Assemble and coordinate project staff.

Skills

Project management

Clinical research

Knowledge of ICH/GCP/FDA regulations

Risk management

Budget management

Education

Bachelor's degree or equivalent in medicine, science or relevant discipline

Master's degree

Tools

MS Word

Excel

PowerPoint

Job description

About the job Senior Project Manager - Med Device

Our client is a well funded start up in the cardiac space and is looking for an experienced project manager to work closely with the executive team. This is a contract role and will require travel to North Carolina, Minnesota and California on a regular basis. The ideal candidate will reside near a major airport.

A DAY IN THE LIFE

• Planning and implementation of cross-functional projects within medical device including cardiovascular device trials.
• Facilitate the definition of project scope, goals and deliverables
• Define project tasks and resource requirements.
• Develop full-scale cross-functional project plans.
• Assemble and coordinate project staff
• Plan and schedule project timelines
• Develop and Manage Risk Mitigation Strategies for projects
• Constantly monitor and report on progress of the project to all stakeholders
• Implement and manage project changes and interventions to achieve project outputs
• Project evaluations and assessment of results
• Manage project study budgets and invoicing procedures according to study contract

Requirements:

• At least 4 years' experience in medical device / pharma clinical research Industry required
• At least 2 years' project management experience
• At least 1 year experience in a managerial role
• Experience of managing cardiovascular device trials preferred
• Knowledge of ICH/GCP/FDA regulations and guidelines for medical devices and/or pharmaceutical/biologic agents
• Bachelor's degree or equivalent in medicine, science or relevant discipline required. Masters degree preferred. PMP or six sigma preferred
• Proficient in computer applications such as MS Word, Excel, Publisher, PowerPoint