Real-world Evidence Analyst I

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.

Thanks to our Business growth Cerner Enviza is looking for a new talented Real-World Evidence Analyst I (A). In this role, you will be a member of the Project Team for international studies.
This role requires collaboration within a matrix international environment, proactive internal and external communication, and exceptional strategic planning, risk management and organizational skills.

MISSION

Contributes under the supervision of a Data Manager and/or Data Management Director, to the data management steps database set up (data entry, user acceptance test), database conduct (queries management) and database close-out on different type of studies.
Performs data entry and manages data entry staff
Performs data quality checks to verify accuracy.
Writes/edits data management documents: Data Management Plan, Data Validation Plan, Data Management report, Quality control report
Interacts with Data Management team and/or data management subcontractor and project teams according to projects.
Manages users account
Essential ICH documents for the conduct of trials (before, during and at the end of the trial). RGPD in Clinical Research
Database design, from the CRF
Quality control, data validation, coding and dictionaries, laboratory data, database lock
CDISC and SDTM standards, Risk Based Monitoring

**Working Environment**:

- Hybrid & Onsite: No Relocation Assistance OfferedThis 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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**Cerner Jobs and Careers**:
**Additional Information**:
**Working Environment**
- Hybrid & Onsite: No Relocation Assistance Offered**Relocation Assistance Available for this Job**:

- No**Qualifications**: Qualifications:
- Bachelor's Degree in scientific discipline or health care preferred;
- Already an experience in a bio/pharma./CRO;
- Fluency English (C2);
- Excellent planning, organizational and problem-solving skills;
- Excellent communication skills - able to distill issues, manage client expectations and act as a trusted advisor in a timely manner;
- Ability to work effectively in a team in a fast-paced and dynamic environment;

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.