Job Description

Veranex’s mission as an Innovation CRO is to improve patient outcomes by accelerating our clients’ innovations to market. As the world’s only end-to-end professional services firm focused on MedTech, we take clients’ Vision to Velocity through our comprehensive service portfolio, with expertise in human centered design and product development, preclinical and clinical research, regulatory affairs, and market access and reimbursement consulting.

About This Role:
Veranex has an exciting opportunity to join our team as a Clinical Data Coordinator 2. You will be part of a team working to improve lives globally through medical technology innovation. The Clinical Data Coordinator 2 for data entry activities, quality control reviews, and identification and documentation of data issues. Executes data validation programs and reports to facilitate data review. Participate in data management activities from study set up to database lock. Generates data queries to resolve data discrepancies. Appropriately addresses responses to data queries and accurately updates the clinical data as necessary. Performs validation of edit check programs. Participates in study close-out activities through data review, query resolution, and addressing issues to lock database.
What You Will Do:
• Performs study status tracking, data entry and verification.
• Performs data review and quality control procedures.
• Develops and provides input into project specific guidelines.
• Performs data review, identification of data issues, and quality control procedures.
• Participates in User Acceptance Testing.
• Participates in the query management and data cleaning process.
• Archives all study related documents.
• Provides advice or solutions in area of expertise.
• May participate in audits and inspections.
• Participates in project team meetings.

Qualifications:
Required skills:
• Bachelor’s degree or international equivalent in life science.
• 2 - 4 years of relevant work experience
• Developing professional expertise, applying company policies and procedures to resolve issues.
• Works on routine problems of moderate scope.
• Exercises judgment following standard practices and procedures in analyzing situations or data from which answers can be readily obtained.
• Build stable working relationships internally.

Preferred:
• Working knowledge of clinical research and the drug development process.
• Working knowledge of databases, tracking, validation, programming, word processing and spreadsheet software.
• Working knowledge of clinical databases and query management
• Working knowledge of organization procedures and policies and ensures actions comply.
• Good written and oral communication skills
• Good attention to detail
• Good organization and time management skills
• Ability to take a proactive approach to work
• Ability to solve simple to moderate problems
• Ability to multitask and prioritize work
• Good ability to work in cross-functional teams

Veranex is an equal opportunity employer and prohibits discrimination of any kind. All qualified applicants will receive consideration for employment without regard for race, color, religion or belief, sex (including pregnancy, gender identity or gender expression), sexual orientation, parental or marital status, disability, age, status as a protected veteran, national, social, or ethnic origin, or any other applicable legally protected characteristics.