🌎
This job posting isn't available in all website languages

NV Clinical Research Project Manager

📁
Clinical
📅
170006WB Requisition #
Thanks for your interest in the NV Clinical Research Project Manager position. Unfortunately this position has been closed but you can search our 1,333 open jobs by clicking here.

MAIN JOB DUTIES/RESPONSIBILITIES (Please list most important duties first)

·         Assist with overall successful conduct of assigned clinical studies consistent with applicable regulations, guidelines, and policies. 

·         Assist in preparation of sections of the Investigational Plan for assigned clinical studies. 

·         Assist in preparation of study materials and/or training (e.g., training of investigators, site staff and Medtronic field staff). 

·         Interface with, and assure training of investigators, site staff, and Medtronic clinical staff. 

·         Conduct site initiation (e.g. start-up document preparation, distribution, receipt, and review).  Set-up and maintain accurate study status and implant logs. 

·         Conduct site monitoring

·         Interfaces with representatives from key functional groups (Research & Development, Manufacturing, Sales, Marketing, Regulatory Affairs, and European Clinical Groups). 

·         Assist in preparation of study budget and project plans. 

·         May arrange conference calls, staff meetings and training events. 

·         Assist in compilation and review of adverse event information. 

·         Assist in follow-up and resolution of site issues noted by field staff. 

·         Assist in compilation, review and conclusion of device complaints. 

·         Assist in study closure activities (e.g. close-out document preparation, distribution, receipt and review, audit and archive). 

·         Assist data management group with review of clinical data/information and oversight of data correction. 

·         Assist in preparation of annual, interim and final reports and presentations. 

·         Provide oversight of activities performed by Contract Research Organizations (e.g. CROs, core labs). 

·         Able to refer to Standard Operating Procedures (SOPs) and Department Operating Procedures (DOPs) for guidance on everyday study tasks. 

·         Participate in training to enhance knowledge base.

My Profile

Create and manage profiles for future opportunities.

Go to Profile

My Submissions

Track your opportunities.

My Submissions

FORTUNE NAMES MEDTRONIC TO 'CHANGE THE WORLD' LIST

FORTUNE puts Medtronic among the top 20 companies worldwide having a positive social impact through core business strategy.

Read The Story

ENGINEERING

Bring your talents to help us build life-changing technology

LEARN MORE

Three Women Working

INCLUSION AND DIVERSITY

We believe that when people from different cultures, genders, and points of view come together, innovation is the result — and everyone wins. Medtronic walks the walk, creating an inclusive culture where you can thrive.

SEE HOW