Clinical Project Manager

SCIRENT Clinical Research and Science; Berlin; Vor Ort; EUR 90.000 - 110.000; Vollzeit

Benefits dieser Stelle

Company pension

Welcome trips for newcomers

In-house training

Offices across Europe

Berlin office in heart of city

Zusammenfassung

SCIRENT Clinical Research and Science is seeking a dedicated Clinical Project Manager for a full-time role in Germany, focusing on cardiovascular trials. You will lead planning, coordination, and execution, and serve as the primary point of contact for sponsors, investigators, and internal teams to ensure timely, compliant study delivery.

Key responsibilities include managing timelines, budgets, resources, and quality, while ensuring regulatory compliance.

Qualifikationen

• Bachelor’s degree or higher in life sciences or related field.
• CPM experience in clinical research is required.
• ICH/GCP certification is mandatory.
• Experience with cardiovascular trials is a strong asset.

Aufgaben

• Lead study planning, timelines, and budget management.
• Coordinate cross-functional teams and external partners.
• Ensure high-quality, regulatorily compliant trial execution.
• Maintain sponsor and stakeholder communications.
• Prepare for audits and inspections.
• Monitor risk, escalate issues, and implement corrective actions.

Kenntnisse

Project management

Leadership

Regulatory knowledge

Cross-functional collaboration

Communication

Risk management

Quality mindset

Ausbildung

Bachelor’s degree or higher in life sciences or related field

ICH/GCP certification

Jobbeschreibung

SCIRENT Clinical Research and Science is seeking a dedicated Clinical Project Manager for a full-time position in Germany.

As a Clinical Project Manager, you will be responsible for the planning, coordination, and execution of clinical trials in the cardiovascular field. You will be the primary point of contact for internal teams, external partners, and sponsors, ensuring that they work together smoothly across all project phases. You will oversee timelines, budgets, resources, and quality to ensure studies are delivered on time and in compliance with applicable regulations. Working closely with cross-functional teams, you will coordinate operational activities, address project-specific challenges, and support regulatory requirements. Ideally, you bring experience from working in large CROs. The position is ideally based in Berlin, but we also welcome applications from candidates who are willing to relocate.

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Area of Responsibility

• Team Leadership: Serve as the key contact for the German study team and ensure seamless communication between international project leads and the local team (e.g., CRAs).
• Stakeholder Communication: Serve as the primary liaison between sponsors, investigators, and internal departments, maintaining a focus on clinical objectives.
• Quality and Compliance: Ensure high-quality execution of studies, adherence to timelines, budgets, and strict compliance with regulatory requirements.
• Risk and Progress Management: Monitor study progress, manage risks, initiate corrective actions, and lead escalation processes where necessary.
• Audit Readiness: Prepare for and support audits and inspections, ensuring full regulatory compliance throughout the study lifecycle.
• Budget and Documentation Oversight: Supervise study budgets, contractual obligations, and maintenance of essential study documentation.

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Your Profile

• Education: Bachelor’s degree or higher in life sciences, medicine, or a related health field, ideally with specialization or strong focus on cardiology or cardiovascular research.
• Experience: Proven experience as a Clinical Project Manager in clinical research is required. Familiarity with cardiovascular trials is a strong asset.
• Certifications: ICH/GCP certification is mandatory.
• Skills: Strong project management and leadership abilities, excellent communication skills, and a proactive, solution-oriented mindset.
• Language Proficiency: Fluent in English and German. Additional languages (Greek, Italian, or a Scandinavian language) are a plus.
• Personal Traits: Independent, well-organized work style with a strong commitment to advancing healthcare through high-quality clinical research.

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What We Offer

• Compensation: Attractive salary and a company pension scheme.
• Onboarding: Welcome trips to our partner countries and newcomers meet & greet – ensuring your smooth start.
• Training and Development: We offer extensive in-house training across all areas of clinical research. Voluntary language courses and regular coaching sessions are available to support your continuous development.
• Work Environment: Access to offices throughout Europe, equipped with laptop and phone.
• Location: Our modern office in the heart of Berlin is perfectly connected and easily accessible.

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About us

SCIRENT was founded in 2012 with the vision of helping customers develop innovative medical drugs and devices for patients with cardiovascular diseases. Our dedicated team of experienced clinical and regulatory professionals share their enthusiasm for developing effective therapies for cardiac patients. What sets us apart from our competitors is our profound expertise in cardiovascular therapy and diagnostics. Our CRO offers access to an impeccable network of dedicated trial centers in Europe and North America with extensive experience in cardiovascular studies. Our customers appreciate our lean and agile management, which generally makes our performance faster and more efficient.