Contractor PM-Tigermed Jyton-Spain (MJ000038)

Tigermed; Madrid; Presencial; EUR 45.000 - 65.000; Jornada completa

Descripción de la vacante

A leading clinical research organization in Madrid is seeking a skilled project manager for clinical trials. You will implement project management plans, oversee trial activities, and foster relationships with sponsors and investigators. Candidates need a bachelor’s degree in a relevant field and at least 5 years of clinical trial experience, including independent project management. Fluency in English and a GCP certificate are required.

Formación

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

Responsabilidades

• Draft and implement project management plan according to SOPs and regulations.
• Ensure trial is managed under the project management plan.
• Ensure CRA is trained on the monitoring plan.
• Manage site feasibility, site selection, initiation, monitoring, and close-out activities.
• Maintain positive relationship with sponsor and investigator.

Conocimientos

Project management

Communication skills

Information-gathering skills

Time management skills

Educación

Bachelor degree in Medical, Pharmacology or Biology

Herramientas

Microsoft Office

Descripción del empleo

Job Purpose

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

• Academic / Major - Bachelor degree or above in Medical, Pharmacology or Biology related majors.
• Professional Skills - Adequate knowledge of medical device development, including local regulation, GCP. GCP certificate required.
• 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.
• Fluent in both written and oral English.
• Good command of Microsoft offices.
• Other abilities such as Communication skills, Information‑gathering skills, Strong project management skill; Strong time management skill.