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Sr. Clinical Research Associate (Germany)

Alimentiv

Job Location:

Berlin - Germany

Monthly Salary: Not provided by the employer

Posted: 9 July 2026 (30+ days ago)

Application Deadline: 6 November 2026

Vacancies: 1 Vacancy

Job Summary

Manage deliver and/or perform full clinical site monitoring services for one or more projects which may include multiple services be complex in nature and/or run on a multinational -house based position responsible for the design and oversight of project monitoring services including training site/patient recruitment site data/document management monitoring project site budgets and regulatory filings that aligns with SOPs study guidelines and GCP best the function of Lead CRA will act as primary liaison between CRAs and project team and may be required to participate in the development of project plans protocols CRFs communications or other monitoring forms documents and tools. Represents the corporation by maintaining collaborative relationships with stakeholders.

Monitoring - Subject Expert

Act as subject matter expert mentor coach and/or provide performance feedback to manager for peers.
Assist with selection hiring training and supervision of CRAs as needed. Perform co-monitoring and training visits with CRAs.
When required act as the first escalation point for the resolution of site/patient issues or to address Sponsor concerns.
May represent Director Monitoring and Site Management or Manager Clinical Site Management in BD initiatives with a site monitoring focus.

Site Recruitment and Setup

Identify and recruit site investigators coordinate the movement and delivery of trial materials samples tests and forms including investigational product protocols SOPs CRFs project documents forms and support tools.
Ensure SOPs in place to optimize patient recruitment providing guidance to site teams of inclusion/exclusion criteria.

Investigational Site Monitoring

Primary clinical site contact.
May act as primary contact for any questions or issues that arise from investigational sites.
Oversee overall integrity of the study to promote positive working relationships with the site and staff.
Facilitate and support site staff with access to study systems and ensure sites are compliant with project specific training requirements.
Ensure all site related issues are followed until resolution.
Coordinate delivery of clinical sites communications collaborating with project teams to ensure investigational sites are provided accurate ongoing data updates information and feedback on project/regulatory guidelines and objectives throughout the project lifecycle.

Qualifications

The successful candidate will possess a minimum of a college diploma/degree and 4-6 years of related experience.
Self-motivation with strong communication skills and a commitment to achieving positive results.
Strong attention to detail and keenness to understand the importance of building collaborative relationships to achieve results.
Critical thinking abilities
Ability to regularly travel to study sites approximately 58 days per month depending on project and business needs.

Working Conditions

Home-based
Regular travel is required

Stay Alert to Recruitment Scams
We have been made aware of individuals posing as our recruiters and contacting candidates with fraudulent opportunities. Our hiring process always includes direct engagement with a recruiter or hiring manager and we will never ask for sensitive personal information early in the process. Official communication will only come from our company email domains. If something doesnt feel right we encourage you to verify before responding.

We may use artificial intelligence (AI) tools to support parts of the hiring process such as reviewing applications analyzing resumes or assessing responses and identifying potential inconsistencies or verification signals in application materials based on available information. These tools assist our recruitment team but do not replace human judgment. Final hiring decisions are ultimately made by humans. If you would like more information about how your data is processed please contact us.

Required Experience:

Senior IC

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