Clinical Project Manager

SCIRENT Clinical Research and Science; Berlin; Vor Ort; EUR 60.000 - 100.000; Vollzeit

Zusammenfassung

A leading clinical research organization is seeking a dedicated Clinical Project Manager for a full-time position in Berlin, Germany. This role involves planning and overseeing clinical trials in the cardiovascular field, serving as a primary contact for teams and sponsors. Ideal candidates hold a Bachelor's degree in life sciences and have proven project management experience, particularly in cardiovascular trials. The position offers a competitive salary, training opportunities, and a supportive work environment.

Leistungen

Attractive salary

Company pension scheme

Extensive in-house training

Voluntary language courses

Qualifikationen

• Proven experience as a Clinical Project Manager in clinical research.
• Experience with cardiovascular trials is a strong asset.
• ICH / GCP certification is mandatory.
• Fluent in English and German; additional languages are a plus.

Aufgaben

• Serve as the key contact for the German study team and ensure seamless communication.
• Maintain focus on clinical objectives as the primary liaison between stakeholders.
• Monitor study progress, manage risks, and lead escalation processes.
• Prepare for and support audits and inspections.

Kenntnisse

Project management

Leadership abilities

Communication skills

Solution-oriented mindset

Ausbildung

Bachelor's degree in life sciences, medicine, or related field

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.

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.

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.

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.

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.

We look forward to receiving your complete application documents, including the proposed start date of work.

Contact

CEO: Prof. Dr. med. Hans-Dirk Düngen

SCIRENT Clinical Research and Science

Amrumer Str. 16, 13353 Berlin

www.scirent.com