(Senior) Clinical Trial Manager (m/f/d)

HELM AG; Hamburg; Vor Ort; EUR 70.000 - 90.000; Vollzeit

Benefits dieser Stelle

International opportunities

Seminars and further training

Work-life balance benefits

Zusammenfassung

A leading pharmaceuticals company in Hamburg is seeking a (Senior) Clinical Trial Manager to join their team. The role involves overseeing clinical studies, ensuring product efficacy and safety, and collaborating with interdisciplinary teams. Candidates should possess a degree in life sciences, have more than 3 years of clinical research experience, and be proficient in project management tools like MS Office and SAP. This position offers a dynamic work environment with opportunities for professional growth.

Qualifikationen

• Over 3 years of experience in clinical research.
• Ability to manage multiple projects simultaneously.
• Solid understanding of regulatory guidelines.

Aufgaben

• Ensure continuous proof of efficacy and safety of products.
• Provide qualified responses to scientific questions.
• Plan and coordinate clinical studies.

Kenntnisse

Scientific rigor

Effective communication

Project management

Hands-on mentality

English fluency

Ausbildung

University degree in a life-science discipline

Tools

MS Office

SAP or ERP systems

Jobbeschreibung

Experience HELM as a unique family business and an attractive employer. Through a constant exchange of ideas, our ultimate goal is to offer our customers future‑oriented solutions within our global network. At any time, in any place. This allows us to work proactively and think long‑term - in operations, quality management, process optimization, product development and distribution. We are innovation drivers, possibility makers and a reliable partner, all in one.

(Senior) Clinical Trial Manager (m/f/d)

Date: Feb 10, 2026

Location: Hamburg, DE, 20097

Business Unit: Pharma

Job Function: Product Development / Launch Management

Level of Experience: Mid-Career

At HELM Pharmaceuticals, based in the Headquarter in Hamburg, we develop generic pharmaceuticals.

To strengthen our team in the Finished Dosage Form Programs we are looking for a Manager Clinical Development (m/f/d) with a clinical life science background.

In this position, you combine scientific expertise with strategic thinking, you help shape a high‑quality development pipeline and contribute to strong regulatory outcomes. You will work closely with interdisciplinary teams and external partners to drive projects forward efficiently. This role offers you the opportunity to actively influence clinical development decisions and create real value for customers. Become part of a dynamic environment where your work has a real impact!

• You ensure the continuous proof of efficacy and safety for our developed products across all life‑cycle stages.
• Furthermore, you also provide qualified responses to scientific and regulatory questions related to trial design, evidence requirements, and portfolio selection.
• In addition, you will represent our clinical development in interdisciplinary generic development teams with emphasis on clinical trials of medicinal products.
• As Trial Manager, you plan, coordinate, and supervise clinical and/or pre‑clinical studies in line with regulatory guidelines and maintain quality management of the entire trial program. This also includes consultation and design of trial concepts with competent authorities and the preparation of scientific advice packages.
• Part of your role will also include tasks as a Medical Writer, where you prepare and review scientific documentation on the efficacy and safety of our products. Here, you ensure the timely preparation of non‑clinical and clinical documentation for regulatory submissions, including the commissioning and review of modules 2.4 and 2.5.
• In doing so, you respond to deficiency letters during registration procedures and manage corresponding customer inquiries.
• Moreover, you identify, select, commission and collaborate with national and international service providers (CROs, monitors, consultants), including auditing and ensuring proper investigational medicinal product handling in line with GCP and GMP requirements.
• Lastly, you collaborate with the project teams in due‑diligence processes and evaluate dossiers as part of in‑licensing activities.

Your profile:

• You hold a university degree in a life‑science discipline.
• Moreover, you have a solid understanding of clinical research with more than 3 years of experience.
• You combine scientific rigor with a hands‑on mentality and a structured, solution‑oriented way of working.
• You communicate effectively with interdisciplinary teams and external partners and feel comfortable managing several projects simultaneously.
• You are familiar with common IT applications within the framework of project management (MS Office). In top of that, you already gained experience in working with SAP or another ERP system.
• Fluent spoken and written English skills complete your profile.

Every day, each one of us contributes to HELM's success with competence, the highest expertise and unique service. We reward this commitment - not only with international opportunities, possibilities for seminars and further training but also with benefits that offer optimal conditions to reach the perfect work‑life balance.

Interested?

Join our motivated team and help shaping the future of HELM! Even if you do not fulfil all of the requirements in our profile, we encourage you to apply. It is important to us to find the right people who will enrich our team with their motivation and personality!

We look forward to receiving your application with all the necessary documents via our application portal.