Natural scientist (m/f/d) or healthcare professional (m/f/d) as Clinical Research Associate (ca[...]

GCP-Service International Ltd. & Co.KG; Siegburg, Bremen; Hybrid; EUR 45.000 - 60.000; Vollzeit

Zusammenfassung

A private contract research organisation is looking for a Clinical Research Associate (m/f/d) in Siegburg or remotely. This role involves supporting trial sites, ensuring study compliance, and conducting monitoring visits. Candidates should have a degree in natural sciences or medical training, with fluency in German and English. The position offers flexible working conditions, training opportunities, and attractive remuneration. If you're proactive and eager to help develop new medical solutions, this opportunity is for you.

Leistungen

30 days of holiday

Flexible working hours

Company mobile phone

Company pension scheme

Qualifikationen

• Experience in clinical research is an advantage but not a prerequisite.
• Ability to quickly familiarise with new software tools.
• Possibility to travel up to 50% of working time in Germany and Europe.

Aufgaben

• Support and training of trial sites in clinical trials.
• Ensure studies are conducted in accordance with protocols and regulations.
• Monitoring visits to review study documents and patient records.
• Preparation of reports and measures in case of deviations.

Kenntnisse

Fluent in German

Fluent in English

Excellent communication skills

Attention to detail

Self-organisation

Ausbildung

University degree in natural sciences or vocational training in the medical field

Tools

Software tools

Jobbeschreibung

Natural scientist (m/f/d) or healthcare professional (m/f/d) as Clinical Research Associate (career starter or experienced CRA)

About us

GCP-Service was founded in 2004 and is a private contract research organisation. We offer our customers full-service solutions for clinical trials to bring innovative drugs, medicaldevicesand in-vitro diagnostics tothemarket quickly.

Tasks

• Support and training of trialsites(clinics or general practitioners) in the implementation of clinical trials
• Ensure that studies are conductedin accordance withthe protocol, SOPs, ICH-GCP and all applicable regulatory requirements 7
• Monitoring visits to the trialsitesto review study documents and patient records
• Preparation of reports and initiation of measuresin the event ofdeviations and violations
• Supporting the studysitesas the primary contact for the study

Qualificationprofile

• University degree in natural sciences/healthcare or vocational training in the medical field
• Experience in clinical research is an advantage, but not a prerequisite for career starters. ApplicationsfromexperiencedCRAsarealsowelcome.
• Fluent in German and English (written and spoken)
• Excellentcommunicationandpresentationskills
• Ability to quickly familiarise yourself with new software tools
• Highdegreeofself-organisation
• Supportive personality with attention to detail
• Possibility to spend up to 50% of working time travelling in Germany and Europe. A positionas a Remote CRA with a low amount of travelling is also possible.

Weoffer

• Workplace: Home office or office workplace in Bremen or Siegburg
• Employment: Permanent position, preferably full-time
• Work-life balance: self-organised work, flexible working hours, 30 days holiday
• Remuneration: attractiveremunerationwith good career opportunities
• Additionalbenefits: BahnCard, company mobile phone and other equipment, company pension scheme
• Individual development: CRA training for career starters, individual opportunities for internal further training
• Our values: respectful and honest interaction with one another, short decision-making processes, tolerance, reliability

We are looking for talented people who are proactive and enjoy working with modern software. If you have the desire to start an exciting career and the passion to help us develop new drugs, medicaldevicesand in-vitro diagnostics, please contact us today!

Thank you for submitting your application. We truly appreciate your interest in joining our company.

Please note that the review process may take some time. If you are selected to move forward, we will contact you within two weeks. If you are not selected, please understand that we will not be sending additional updates.

In accordance with the application procedure (Art. 6 para. 1b GDPR), we will retain your application documents for a period of six months. After this time, your data will be securely deleted. You have the right to request access to, rectification, or deletion of your personal data, to restrict or object to its processing, and to request data portability.

If you have any questions regarding data protection, please contact our Data Protection Officer at [e-mail].

We wish you all the best in your job search.

Best regards,

HR team @ GCP-Service International

If we have piqued your interest, we look forward to receiving your application. Please address it as follows, stating your salary expectations and the earliest possible starting date: