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Clinical Research Associate

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Remote from
Germany
Salary
Undisclosed
Employment
Full Time
Experience
Senior
Published
Apply before
21 Nov 2026
Listing views
34
Application actions
1
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AI Summary

The role, at a glance.

Precision Medicine Group is hiring a Clinical Research Associate to monitor oncology and rare-disease clinical studies at investigative sites in Germany. The CRA will oversee site progress, support study start-up and regulatory activities, conduct monitoring visits, and ensure compliance with protocols, SOPs, ICH-GCP, and applicable regulations. Candidates need a scientific or healthcare degree, at least six months of relevant CRA or site-management experience, oncology experience, and fluency in German and English. The position is remote within Germany but requires substantial domestic travel, including overnight stays, estimated at 50–60%.

Role DNA

A quick view of the complexity, pace, ownership and collaboration implied by the job description.

Job Complexity

4/5
EasyHard

Pace & Pressure

4/5
RelaxedFast-paced

Autonomy Level

4/5
GuidedFull ownership

Communication Load

5/5
IndependentCollaborative
AI insightThe role combines regulated clinical-trial oversight, quality accountability, site coordination, and significant travel. Success requires sound independent judgment while maintaining rigorous ICH-GCP and protocol compliance.

Salary analysis

Estimated compensation compared with the broader US market for similar roles.

Estimated job median (per year)Market rate
$65,000
US market range (per year)$55k–$80k
AI insightThe yearly pay period is inferred from the job context; it was not explicitly stated by the employer. No employer salary was disclosed. Estimated annual compensation for a Clinical Research Associate in Germany is €55,000–€80,000; the displayed USD-equivalent estimate uses the configured analysis market and is illustrative only.

Core skills

Skills and capabilities most closely associated with this opportunity.

Sample interview questions
How do you ensure that an investigative site remains compliant with a study protocol and ICH-GCP requirements?

I prepare thoroughly by reviewing the protocol, monitoring plan, prior visit reports, and outstanding action items before each contact. During visits, I verify source data, informed-consent documentation, investigational product accountability, and essential documents, then document findings clearly and agree on corrective actions with the site.

Describe how you would manage a site that is falling behind on enrolment or has unresolved data queries.

I would first determine the root causes through a focused discussion and review of screening, recruitment, and data-management processes. I would create a practical recovery plan with measurable actions, timelines, and escalation points, while keeping the project team informed of risks and progress.

What steps would you take when identifying a potential protocol deviation?

I would promptly assess participant safety and the deviation's impact on data integrity, verify the available source information, and notify the investigator and internal study team according to the study procedures. I would ensure it is documented, reported where required, and followed by appropriate corrective and preventive actions.

How do you balance independent work with communication across a clinical project team?

I prioritize and manage my monitoring activities independently, but communicate risks, milestones, and decisions early through concise written updates and scheduled team discussions. This keeps sites supported and ensures project stakeholders can address issues before they affect timelines or quality.

Why is oncology experience important for this CRA position?

Oncology trials often involve complex eligibility criteria, safety monitoring, biomarkers, and time-sensitive treatment pathways. Relevant experience helps a CRA recognize study-specific risks, communicate effectively with sites, and protect both participant safety and data quality.

This analysis is generated from the job description. Salary estimates, role characteristics and sample answers are guidance, not employer-provided facts.
Opportunity details

About this role.

Precision for Medicine, Oncology and Rare Disease is not your typical CRO. We are passionate about cultivating our culture and are proud to share extremely high CRA retention rates compared to industry averages. We are now recruiting Clinical Research Associates (different seniority levels) to join our team in Germany.

CRAs join us, love their jobs, and stay because of the amazing people and enjoyable quality of life. You will focus on an average of one to two studies setting you up to be a protocol expert. Travel is reasonable and your work/life balance will benefit as a result. Most meaningfully – your voice will be heard. Working in a smaller CRO allows you to have influence and impact when it matters most and support from direct line management.

About you:

  • You are calm, thoughtful, and responsive when things don’t go as planned.
  • You are well-prepared, whether it be for an investigator meeting, site visit or project team update, always staying two steps ahead of the game.
  • You find quick and creative ways of overcoming difficulties.
  • You have an impeccable eye for detail.
  • You identify potential study risks and propose solutions on how to mitigate them.
  • You take responsibility in the quality and outcomes of your work.
  • You are adept at handling conflict by using tried and true resolution strategies.

How we will keep you busy and support your growth:

You will monitor and own the progress of clinical studies at investigative sites and ensure that clinical studies are conducted, recorded, and reported per protocol, SOPs, ICH-GCP, and all applicable regulations and standards. You will coordinate all necessary activities required to set up and monitor a study (i.e., identify investigators; helping prepare regulatory submissions, conducting pre-study and initiation visits, etc.).

Qualifications:

Minimum Required:

  • Graduate or postgraduate degree with a concentration in a scientific or healthcare discipline
  • At least 6 months of experience as a CRA in either a CRO or pharmaceutical/biotech industry or equivalent, relevant experience and/or demonstrated competencies. Site management or equivalent experience in clinical research.

Other Required:

  • Excellent communication and organizational skills are essential. A team player.
  • Evidence of a client focused approach.
  • Availability for domestic travel including overnight stays, which may constitute up to approximately 50-60% travel commitment (international travel may be required for some senior level positions)
  • Fluency in English and German
  • Experience in oncology

Preferred:

  • Study start up activities experience
  • CAR-T or FIH – phase III
  • Medical device experience

#LI-EK1 #LI-Remote

Please, apply in English.

Precision for Medicine, Oncology & Rare Disease is a precision medicine CRO. Precision’s uniquely integrated offering enables the science of precision medicine by combining novel clinical trial designs, industry-leading operational and medical experts, advanced biomarker and data analytics solutions, and an unequivocal real passion for rare diseases and oncology.

Precision medicine is revolutionizing the attack on cancer—and we are passionate about helping you harness its power. We strike tumors on a molecular level using biomarkers to link specific mutations to specific treatments. We combine deep science with deep data from advanced technological platforms, then layer on specialized expertise in the design and execution of targeted, adaptive clinical trials. Ultimately, we deliver robust insights that inform real-time decisions—and optimize the oncology development pathway.

We invite you to learn more about our growing organization serving our clients that are researching groundbreaking cancer therapies. We strive to ensure employees feel appreciated for the contributions they make every single day. You will provide input and have your ideas valued and nurtured, impacting positive change for the company.


Any data provided as a part of this application will be stored in accordance with our Privacy Policy. For CA applicants, please also refer to our CA Privacy Notice.

Precision Medicine Group is an Equal Opportunity Employer. Employment decisions are made without regard to race, color, age, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status or other characteristics protected by law.

If you are an individual with a disability and require a reasonable accommodation to complete any part of the application process or are limited in the ability or unable to access or use this online application process and need an alternative method for applying, you may contact Precision Medicine Group at myHR@precisionmedicinegrp.com.

Recruitment Fraud Warning: Please be aware that fraudulent individuals and websites may impersonate Precision Medicine Group or its affiliates and attempt to obtain personal, financial, or banking information through fake job postings or employment offers. Precision Medicine Group will never request payment, banking details, or other sensitive financial information as part of the recruitment process. If you believe you have been targeted by a recruitment scam, we encourage you to report the incident to your local law enforcement authorities, consumer protection agency, or relevant cybercrime reporting organization in your country. Please also notify us at myHR@precisionmedicinegrp.com so we can investigate and take appropriate action.

Candidates must be legally authorized to work in the country of employment without employer sponsorship.

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This job listing has been manually reviewed by the Jobicy Trust & Safety Team for compliance with our posting guidelines, including verification of the company's legitimacy, accuracy of job details, clarity of remote work policy, and absence of misleading or fraudulent content.

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