Clinical Research Start-up Project Manager Europe

Biomapas; España; A distancia; EUR 45.000 - 65.000; Jornada completa

Descripción de la vacante

A leading clinical research firm is looking for a Start-up Project Manager. You'll manage clinical trial start-up activities, oversee regulatory submissions, and serve as the primary client contact during trials. The ideal candidate will have strong experience in EU regulatory processes, particularly for multicounty studies. The role offers remote work flexibility and opportunities for professional growth.

Servicios

Performance-based annual bonus

Remote Work, Workation & Flexibility

Health & Wellbeing initiatives

Professional growth and development

Comprehensive Insurance

Formación

• Strong understanding of the EU CTR and CTIS submission process.
• Proven experience as a Start-up PM or lead within a CRO.
• Exceptional communication skills.

Responsabilidades

• Manage oversight of start-up activities within assigned projects.
• Oversee preparation and submissions of clinical trial applications.
• Act as primary contact to clients during start-up trials phase.

Conocimientos

Understanding of EU CTR and CTIS submission process

Experience in managing multicounty studies

Knowledge of ICH-GCP

Organizational and time-management skills

Fluent in English

Descripción del empleo

Clinical Research Start-up Project Manager Europe

Future Opportunity: Start-up Project Manager

At Biomapas, we are continuously expanding our Clinical Trial projects, and this means we are always on the lookout for talented Start-up Project Manager to join our team. While we may not have an immediate opening, we are proactively seeking experienced Start-up Project Manager who see themselves as part of our growing team. If you are passionate about clinical research, project leadership, and working in an international environment, we invite you to submit your application today. We will get in touch when a suitable opportunity arises!

As a Start-up Project Manager you will be responsible for leading and oversight deliverables for clinical trials start-up activities in accordance with ICH GCP, EU CTR requirements CTIS (Part I and Part II), and local countries level regulatory requirements where your expertise will shape operational efficiency.

You must submit your CV in the English language for consideration.

Responsibilities

• Projects SUPM oversight: manage oversight of start-up activities (starting from feasibility completed till sites' activation) within assigned projects
• CA and EC submissions management: oversee the preparation and submissions of clinical trial applications under EU CTR and other applicable country level regulatory requirements
• Site start-up management: supervise sites documents collection for CA and EC submissions and for IP release /essential documents packages
• Client management: acting as the primary point of contact to the Clients during start-up trials phase, developing trials SSU timelines and submission strategy in collaboration with the Clinical Project Manager and the Client
• Cross-functional leadership: coordinate trial start-up activities in close cooperation with Clinical Operations, Regulatory Affairs, Contracts & Budgets, Vendor Management departments
• Risk & Time management: develop and maintain SSU strategy and timelines as per committed to Clients' deliverables. Timely identify potential bottlenecks or study start up processes, suggest and implement mitigations strategies

Requirements

• Strong understanding of EU CTR and CTIS submission process, proven experience of submissions done via CTIS (Part I and Part II)
• Proven experience being a Start-up PM, Start-up lead within CRO, managing multicounty studies
• Strong knowledge of ICH-GCP, local regulatory frameworks, and clinical trial lifecycle
• Exceptional organizational, time-management and communication skills
• Managing start-up activities in multicounty or global trials is a major plus.
• Ability to work both independently and as a key trial team member
• Experience managing start-up activities in Ukraine, Georgia, Kazakhstan Armenia, or similar emerging clinical research regions is a plus
• English fluent, local languages proficiency is an advantage

Benefits

• International team and environment
• Performance based annual bonus
• Remote Work, Workation & Flexibility
• Health & Wellbeing - wellness initiatives
• Professional growth and development in the Life science industry
• Team Culture - Team buildings, global meetings, and B Active events
• Comprehensive Insurance - Personal accident, business trip coverage, and additional health insurance