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Lead CRA (m/f/d)

Munich, Bavaria, Germany

Job Description

Cerner Enviza, an Oracle company is a leading global healthcare consulting firm and trusted advisor to many of the world’s top pharmaceutical, biotech, and medical device & diagnostic companies. By supporting the work of Cerner Enviza, you will work with world-class healthcare companies, helping them improve global access to medicines by connecting science and research. Cerner Enviza is passionate about our people, our business, and our clients and is proud to foster a culture that contributes to the health and well-being of humankind.

With ongoing and ground-breaking developments in Oncology and Rare Disease, an increased focus on more scientific, targeted medicine and continuous integration of technology into development and delivery of medicine, there has never been a more exciting time to work in Life Sciences and, with Cerner Enviza immersed in all of these, there has never been a better time to join us and make a difference to our clients and the lives of patients.

What you will do:

The Lead Clinical Research Associate (CRA) is a critical hire for our business! The healthcare research space is becoming increasingly important, and you will have the chance be part of an industry that is continuing to evolve and grow. This is a great opportunity for someone with a few years of relevant experience to expand on their knowledge while working for a global corporation.

The Lead CRA will work closely with the Project Manager to lead the study site management activities according to GCP and relevant SOPs, ensuring the overall quality and timeliness of deliverables for assigned clinical and non-interventional studies.

The Lead CRA acts as the main contact person to our clients and are responsible for the development of Monitoring plan and training material for CRAs and study sites and the preparation and/or review of essential study documents e.g. Patient Information and Informed Consent Form.

The Lead CRA will coordinate and oversee a team of project-specifically assigned CRAs in different countries and train CRAs on general requirements for the conduct of monitoring activities as well as on study protocol, study-related procedures, adverse event reporting and regulatory documentation.

What we’ll offer

• A competitive salary with exciting benefits

• Flexible and remote working so you can do your best work

• Learning and development opportunities to advance your career

• An Employee Assistance Program to support your mental health

• Employee resource groups that champion our diverse communities

• Core benefits such as medical, life insurance, and access to retirement planning

• An inclusive culture that celebrates what makes you unique

Oracle is an Equal Employment Opportunity Employer. We don’t just value differences—we celebrate them. We’re committed to creating a workplace where all kinds of people work together. We believe innovation starts with diversity and inclusion.

Working Environment

Hybrid & Onsite: No Relocation Assistance Offered

This position offers a Hybrid & Onsite working environment. Meaning you will split working time between a Cerner office or client site and remote. If your current geographical location requires relocating, Cerner will not offer relocation assistance to the specified location. #LI-Hybrid

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Because It's Personal

Time: 2:57

Additional Information

Working Environment Hybrid & Onsite: No Relocation Assistance Offered
Relocation Assistance Available for this Job: No


Basic Qualifications:

At least 4 years total combined related work experience and completed higher education.

Preferred Qualifications:

· A minimum of 3 years of experience as Clinical Research Associate.

· Broad knowledge of different therapeutic areas.

· MS Office Suite (e.g., Word, Excel, PowerPoint).


· Excellent organizational and communication skills.

· Ability to interact professionally with all organizational levels.

· Team player.

· Ability to manage competing priorities in fast paced environment.

· Strong problem-solving skills.

· Read, write and speak fluent English, excellent verbal and written communication skills.

· Willingness to travel on occasion.

All employees must be legally authorized to work in the country where the position is located. Work visa sponsorship is not available for this position.

Cerner is a place where people are encouraged to innovate with confidence and focus on what is important – people’s health and the care they receive. We are transforming health care by developing tools and technologies that make it more efficient for care providers and patients to navigate the complexity of our health. From single offices to entire countries, Cerner solutions are licensed at more than 25,000 facilities in over 35 countries.

Cerner’s policy is to provide equal opportunity to all people without regard to race, color, religion, national origin, ancestry, marital status, veteran status, age, disability, pregnancy, genetic information, citizenship status, sex, sexual orientation, gender identity or any other legally protected category. Cerner is proud to be a drug-free workplace.
If you are an individual with a disability who is unable to use our online tools to search and apply for jobs, and need assistance or an accommodation in the recruiting process, please contact us by calling 866-434-1543 or by emailing

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