Contractor PM-Tigermed Jyton-Germany (MJ000034)

Tigermed; Dortmund; Vor Ort; EUR 60.000 - 80.000; Vollzeit

Zusammenfassung

A leading clinical research organization in Dortmund is seeking an experienced Clinical Trials Project Manager. The role involves implementing project management for clinical trials, ensuring compliance with regulations, and maintaining relationships with sponsors. The ideal candidate must have a Bachelor's degree in a related field, at least 5 years of clinical trial experience, and strong project management skills. This position requires fluency in English and proficiency in Microsoft Office.

Qualifikationen

• Minimum 5 years clinical trial experience with 3 years in independent project management.
• GCP certificate required.
• Fluent in both written and oral English.

Aufgaben

• Draft and implement project management and monitoring plans.
• Manage site feasibility, selection, initiation, monitoring, and close‑out activities.
• Maintain positive relationships with sponsors and investigators.

Kenntnisse

Project management

Communication skills

Information-gathering skills

Time management

Ausbildung

Bachelor degree in Medical, Pharmacology or Biology

Tools

Microsoft Office

Jobbeschreibung

1. Job Purpose

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

2. 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 in 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 of 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.

3. 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) Fluent in both written and oral English.
• (e) Good command of Microsoft offices.
• (f) Other abilities such as Communication skills\Information-gathering skills. Strong project management skill; Strong time management skill.