Contractor PM-Tigermed Jyton-France

Tigermed; Montpellier; Sur place; EUR 50 000 - 70 000; Plein temps

Résumé du poste

A leading clinical research organization in Montpellier is looking for an experienced project manager for clinical trials. You will be responsible for drafting and implementing project management plans, managing site activities, and maintaining relationships with sponsors. The ideal candidate has a Bachelor’s degree in a relevant field, is GCP certified, and has over 5 years of experience in clinical trials. Strong project management and communication skills are essential.

Qualifications

• Proven project management experience in clinical trials.
• 5+ years of clinical trial experience with at least 3 years in project management.
• GCP certification required; adequate knowledge of medical device development.

Responsabilités

• Draft and implement project and monitoring plans according to regulations.
• Manage site feasibility, selection, initiation, monitoring, and closure.
• Maintain positive relationships with sponsors and investigators.

Connaissances

Project management

Communication skills

Time management

Formation

Bachelor degree in Medical, Pharmacology or Biology related majors

Outils

Microsoft Office

Description du poste

Overview

To implement project management of clinical trials effectively, and to ensure success of clinical trials.

Responsibilities

• Make the project management plan: To draft and implement feasible project management plan according to SOPs, ICH GCP Guidelines, ISO14155 and other applicable regulations. Ensure the trial is managed under the project management plan.
• Make monitoring plan: To draft and implement monitoring plan according to SOPs, ICH GCP Guidelines, ISO14155 and other applicable regulations. Ensure CRA is trained on the monitoring plan and the site is monitored based on the monitoring plan.
• Manage site feasibility, site selection, initiation, monitoring, and close-out activities.
• Client Maintenance: Keep positive relationship with sponsor and investigator.

Minimum Qualifications

• a) Academic / Major
  Bachelor degree or above in Medical, Pharmacology or Biology related majors.
• b) Professional Skills
  Adequate knowledge of medical device development, including local regulation, GCP. GCP certificate required.
• (c) Working Experience
  At least 5 years clinical trial experience, at least 3 years of independent project management experience. Experience of at least 3 medical device clinical trials.
• (d) Language
  Fluent in both written and oral English.
• (e) IT Skills
  Good command of Microsoft Office.
• (f) Other abilities
  Communication skills, information-gathering skills. Strong project management skill; strong time management skill.