11 beste Stellen als clinical research study in berlin – aktuell auf Personalsuche

Clinical Research Specialist (CRS)
Evestia Clinical —Berlin
- Hybrides Arbeiten
- Bachelor
- Organisationstalent
- Kommunikationsfähigkeit
Direkt bewerben
6 Tage
Senior Clinical Research Associate
Veranex, Inc. —Berlin
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
Direkt bewerben
Position: Clinical Operations Manager
Meditrial Europe Ltd. —Berlin
- Vollzeit
- Englisch
- Forschungserfahrung
- Master
Project Support - (Temporary Student Contract)
Parexel —Berlin
- Teilzeit
- Informatik
13 Tage
Clinical Operations & Enablement Lead
Nucs AI —Berlin
- Vollzeit
- Hybrides Arbeiten
- Schreibfähigkeiten
- Forschungserfahrung
- Master
Direkt bewerben
Associate Director, Medical Programs
Nucs AI —Berlin
- Vollzeit
- Hybrides Arbeiten
- Forschungserfahrung
- Master
- Projektmanagement
Direkt bewerben
Regulatory Affairs Manager - Pharma/Medical Device
Meditrial Europe Ltd. —Berlin
- Vollzeit
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
Physician Annotator - Nuclear Medicine Clinical AI (Part-Time/Contract)
Nucs AI —Berlin
- Vollzeit
- Homeoffice
- Künstliche Intelligenz
- Flexible Arbeitszeiten
Direkt bewerben
Sr. Project Manager - Scientific RWE Projects (f/m/x)
D4L data4life gGmbH —Berlin
- Vollzeit
- Doktorat
- PMP
- Forschungserfahrung
- Homeoffice-Möglichkeit
18 Std.
Product Designer - Electronic Data Capture and Participant Experience (f/m/x)
D4L data4life gGmbH —Berlin
- Vollzeit
- Forschungserfahrung
- Bachelor
- Mit Reiseanteil
- Homeoffice-Möglichkeit
19 Std.
Medical Lead
dehaze GmbH —Berlin
- Hybrides Arbeiten
- Forschungserfahrung
- Künstliche Intelligenz
Direkt bewerben

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clinical research study jobs near berlin

Clinical Research Specialist (CRS)

Evestia Clinical
Berlin

Direkt bewerben

Details zur Stelle

vor 6 Tagen

Qualifikationen

Bachelor
Organisationstalent
Kommunikationsfähigkeit

Vollständige Stellenbeschreibung

We are building something EPIC

Evestia Clinical is a biotech-focused global CRO delivering authentic expertise and personalized support where client need it most.

Evestia Clinical has recently merged with ICRC-Weyer, an expert life science consultancy based in Berlin, Germany, with over 30 years of experience and we are now expanding our German team.

Our foundation is built on four core principles: Innovation drives us to seek new solutions, Excellence defines the high standards we keep, and genuine Care ensures a supportive culture for both our patients and our people. We foster Partnership in everything we do, believing that working together—with trust and flexibility—is the key to success.

At Evestia Clinical, we combine agility with a people-first approach, empowering our teams to make an impact. As part of our global specialist CRO, you'll help deliver clinical excellence in complex trials while growing your skills in a supportive and collaborative environment.

We are committed to creating development opportunities that allow your skills to grow right alongside ours. If you are inspired by this collaborative environment and ready to change the lives of patients worldwide, we’d love to welcome you to our team.

About the Role

We are looking for a Clinical Research Specialist (CRS) to join our growing team. This cross-functional role is ideal for someone who enjoys variety, has strong organisational skills and wants to play a key role in supporting clinical trials from start-up through to delivery.

What will your job look like?

Provides support to operational departments by completing tasks they have been trained for and assigned in accordance with applicable project plans and Standard Operating Procedures (SOPs).

Set-up, maintenance, and quality control of the project Trial Master File (TMF).

Assists with arranging and participating in project-related meetings and drafting and distributing meeting minutes.

Assisting with the Ethics / Regulatory Submissions; tracking of submissions & approval for the project.

Preparing essential study documents, distributing, tracking, and filing of documents.

Assists with the assignment and tracking of project-related training.

Maintaining understanding of applicable regulations and ICH/GCP guidance.

What will you need to succeed?

Undergraduate degree or equivalent combination of education, training, and experience
Gather and communicate feedback when performing a task in order to ensure acceptability of deliverable

Ability to understand and comply with applicable regulations, ICH/GCP and applicable SOPs

Information technology (e.g. computer proficiency), oral and written communication skills

Maintain strong interpersonal and organizational skills when working with internal and external clients

Ability to seek out their own understanding for more challenging concepts like therapeutic areas or even regulations that may impact their quality in performing a task

Able to cross-reference several data sources of information to identify discrepancies and be able to escalate issues to the appropriate staﬀ

Manage multiple priorities, exhibit a high degree of accuracy, and meet deadlines in a highly dynamic environment.
Excellent written and spoken English, with the ability to communicate professionally with clients and colleagues.

Our Offer

Hybrid-remote with team collaboration days in our Berlin office
A supportive, diverse, and engaged team with flat hierarchies
A permanent contract with a competitive salary and an attractive benefit package

Ready to Take the Next Step?

Does joining Evestia Clinical and making a global impact excite you? Then it's time to apply!

We are eager to meet ambitious candidates. Remember, we hire for potential and passion. Therefore if you feel you're a good fit but don't meet every single requirement, please submit your application anyway. We want to hear from you.

Our Commitment to Inclusion and Diversity

We are deeply proud of our people and the successes we achieve together. We actively seek out and hire individuals with diverse backgrounds, voices, beliefs, and perspectives to join our growing global workforce.

At Evestia Clinical, we believe that each person is unique. We celebrate your individuality, knowing that diverse viewpoints fuel Innovation and drive Excellence. We foster true Partnership across our global teams, guided by genuine Care for our colleagues. Our managers are dedicated to upholding this inclusive environment in every aspect of employment – from hiring and promotion to training and benefits.

It's who we are, it's what we do, it's what we care about.

Equal Opportunity & Accessibility

Evestia Clinical is an equal opportunity employer committed to diversity in the workplace. We ensure fair treatment of all applicants and employees, without discrimination based on actual or perceived race, color, creed, religion, national origin, age, sex, gender identity or expression, sexual orientation, disability, veteran status, or any other characteristic protected by applicable law.

We are committed to providing accessibility accommodations to applicants with physical and/or mental disabilities. If you are interested in applying for employment with us and require an accommodation or special assistance during the application process, please notify our recruitment team by sending an email with your request to [email protected]

Direkt bewerben

Erweiterte Suche

clinical research study Jobs in berlin

Clinical Research Specialist (CRS)

Senior Clinical Research Associate

Position: Clinical Operations Manager

Project Support - (Temporary Student Contract)

Clinical Operations & Enablement Lead

Associate Director, Medical Programs

Regulatory Affairs Manager - Pharma/Medical Device

Physician Annotator - Nuclear Medicine Clinical AI (Part-Time/Contract)

Sr. Project Manager - Scientific RWE Projects (f/m/x)

Product Designer - Electronic Data Capture and Participant Experience (f/m/x)

Medical Lead

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