Clinical Data Associate II

Embedded Shishya; Deutschland; Vor Ort; EUR 45.000 - 65.000; Vollzeit

Zusammenfassung

Precision for Medicine is hiring a Clinical Data Associate II to join our team. Candidates can be based in Hungary, Poland, Romania, Serbia or Slovakia, with opportunities for Germany as well.

The role provides data management support across the full clinical trial lifecycle, under supervision, including CRF development, data entry, QC, and liaison with external vendors. Excellent organizational and communication skills and proficiency in MS Office are required.

Qualifikationen

• Bachelors and/or a combination of related experience.
• Approximately 2 years’ experience as a Clinical Data Associate for a CRO/Pharma/Biotech.
• Proficiency in Microsoft Office: Word, Excel, PowerPoint, Outlook.
• Excellent organizational and communication skills.
• Professional use of English language; both written and oral.

Aufgaben

• Support the Lead DM as a back-up and/or team member, ensuring continuity and timely task execution.
• May perform data entry for paper-CRF studies, as needed.
• May perform quality control of data entry.
• May develop CRF specifications and coordinate stakeholder feedback.
• May assist in building clinical databases.
• Conduct database build UAT and maintain documentation.
• Assist in specifying requirements for edit checks and data review.
• Train clinical research personnel on CRF, EDC, and related items.
• Review and query clinical trial data per Data Management Plan.
• Run patient and study level status and metric reporting.
• May assist with SAS programming and QA of SAS programs.

Kenntnisse

MS Office proficiency

Organizational skills

Communication skills

English proficiency

Ausbildung

Bachelor's degree or equivalent

Jobbeschreibung

Precision for Medicine is hiring a Clinical Data Associate II to join our team. Candidates can be based in Hungary, Poland, Romania, Serbia or Slovakia.

Position Summary:

The Clinical Data Associate II provides data management support and assistance in all aspects of the clinical trial data management process from study start up to post database lock for assigned projects under direct supervision. Standard Operating Procedures / Work Instructions (SOPs/WIs); regulatory directives; study specific plans and guidelines will be followed. This position may perform database development and testing, as well as additional data management activities.

Essential functions of the job include but are not limited to:

• Support the Lead DM as a back-up and/or team member, ensuring continuity, responsiveness, and that tasks are performed in a timely manner
• May perform data entry for paper-CRF studies, as needed
• May perform quality control of data entry
• May develop CRF specifications from the clinical study protocol and coordinate the review/feedback from all stakeholders
• May assist in building clinical databases
• Conduct database build UAT and maintain quality controlled database build documentation
• Assist in specifying requirements for all edit check types e.g. electronic, manual data review, edit checks, etc.
• Responsible for creating, revising, appropriate versioning and maintaining data management documentation.
• Train clinical research personnel on the study specific CRF, EDC, and other project related items as needed
• Review and query clinical trial data according to the Data Management Plan
• Assist in line listing data review based on the guidance provided by the sponsor and/or Lead DM
• Run patient and study level status and metric reporting
• Perform medical coding of medical terms relative to each other in order to ensure medical logic and consistency
• Assist with coordinating SAE/AE reconciliation
• Assist with liaising with third-party vendors such as external data and EDC vendors in a project-manager capacity in support of timelines and data-related deliverables
• May assist with SAS programming and quality control of SAS programs used in the Data Management department
• May assist in identifying and troubleshooting operational problems, issues, obstacles, and barriers for studies based on metrics data, audit reports, and input from project team members and other stakeholders
• May assist in reviewing and providing feedback on protocols, Statistical Analysis Plans (SAP) and Clinical Study Reports (CSRs), if required by the project
• May assist in participating in the development and maintenance of Standard Operating Procedures (SOPs) and corresponding process documentation related to data management and database management activities
• Communicate with study sponsors, vendors and project teams as needed regarding data, database or other relevant project issues
• May present software demonstrations/trainings, department/company training sessions, present at project meetings
• May require some travel
• Perform other duties as assigned

Job Qualifications:

• Bachelors and/or a combination of related experience
• Around 2 years’ experience working as a Clinical Data Associate for a CRO/Pharma/Biotech company.
• Proficiency in Microsoft Office: Word, Excel, PowerPoint, Outlook
• Able to handle a variety of clinical research tasks
• Excellent organizational and communication skills
• Professional use of the English language; both written and oral

Precision for Medicine is the first global precision medicine clinical research services organization, purpose-built to improve the clinical research and development process for new therapeutics. Our novel approach integrates clinical operations excellence, with laboratory expertise, and advanced data sciences to inform every step. We apply our expertise to trials at all stages—from early development through approval—with embedded experience in oncology and rare disease.

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 .