Contractor PM-Tigermed Jyton-Spain (MJ000038)

Tigermed; España; Presencial; EUR 30.000 - 50.000; Jornada completa

Descripción de la vacante

A clinical trial management company in Spain seeks a Project Manager to ensure the success of clinical trials. The candidate must hold a Bachelor’s degree in Medical, Pharmacology or Biology, have at least 5 years of clinical trial experience, including project management, and be fluent in English. Strong project management, communication, and time management skills are essential for this role.

Formación

• 5+ years clinical trial experience.
• 3+ years of independent project management experience.
• Experience in at least 3 medical device clinical trials.
• Fluent in both written and oral English.
• GCP certificate required.

Responsabilidades

• Draft and implement project management plans according to regulations.
• Draft and implement monitoring plans based on regulations.
• Manage site feasibility, site selection, initiation, monitoring, and close-out.
• Maintain positive relationship with sponsor and investigator.

Conocimientos

Project management

Communication skills

Time management

Information-gathering

Educación

Bachelor degree in Medical, Pharmacology or Biology

Herramientas

Microsoft Office

Descripción del empleo

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.