Clinical Data Management Associate II
At Clario, part of Thermo Fisher Scientific, we develop regulated technology that helps unlock better evidence and improve patient outcomes worldwide. Our software platforms support clinical trials, diagnostics, and medical decision-making in highly controlled regulatory environments. The Clinical Data Management Associate II supports the execution of clinical trials by performing day‑to‑day data management activities to ensure accurate, complete, and high‑quality clinical data. This role contributes to database build, data cleaning, query management, and documentation in compliance with SOPs, regulatory requirements, and study timelines, while collaborating closely with Clinical Data Managers and cross‑functional teams.
What We Offer
Competitive compensation
Comprehensive health, dental, and vision coverage
Retirement savings plan with company contribution
Paid time off and company holidays
What You’ll Be Doing
Review and evaluate clinical trial data to ensure accuracy, consistency, and compliance with study requirements
Review project documentation and requirements for new studies and anticipate impacts to Data Management (DM) standards and processes
Collaborate with cross‑functional project teams to stay informed of changes affecting data collection, data cleaning, and data transfers
Define, execute, and review edit checks and resolve discrepant data
Maintain organized, complete, and up‑to‑date study documentation
Create or review Transmittal Forms to ensure consistency with established standards
Develop study data specifications, including data transfer specifications, system configuration specifications, and data validation rules
Identify data errors and inconsistencies and work with project teams to drive resolution
Track outstanding data issues and follow through to resolution
Prepare and validate ad hoc data listings as required
Ensure system defects and enhancement needs are communicated to the appropriate Product Manager and that interim solutions are approved
Provide regular project status updates to the supervisor
What We Look For
Bachelor’s degree in computer science, Life Sciences, or a related field, or equivalent practical experience
At least 1 year of experience in a comparable role within the pharmaceutical, biotechnology, or CRO industry
Working knowledge of relational database structures and data validation principles
Experience using office productivity tools such as Microsoft Word, Excel, and Access
Understanding of clinical trial terminology and regulated environments
Demonstrated problem‑solving and analytical skills
Ability to work independently and collaboratively in a team environment
Strong attention to detail and organizational skills
Effective written and verbal communication skills
Ability to adapt to changing priorities while maintaining a professional and positive approach
Working Conditions
Travel: 0–15%
Lifting: Up to 25 lbs
Extended periods of computer‑based work
At Clario, our purpose is to transform lives by unlocking better evidence. It’s a cause that unites and inspires us. It’s why we come to work, and how we empower our people to make a positive impact every day. Whether you're advancing clinical science, building innovative technology, or supporting our global teams, your work helps bring life-changing therapies to patients faster.
Clario is an equal opportunity employer. Clario evaluates qualified applicants without regard to race, color, religion, gender, national origin, age, sexual orientation, gender identity or expression, protected veteran status, disability/handicap status, or any other legally protected characteristic.
Apply To This Job
What We Offer
Competitive compensation
Comprehensive health, dental, and vision coverage
Retirement savings plan with company contribution
Paid time off and company holidays
What You’ll Be Doing
Review and evaluate clinical trial data to ensure accuracy, consistency, and compliance with study requirements
Review project documentation and requirements for new studies and anticipate impacts to Data Management (DM) standards and processes
Collaborate with cross‑functional project teams to stay informed of changes affecting data collection, data cleaning, and data transfers
Define, execute, and review edit checks and resolve discrepant data
Maintain organized, complete, and up‑to‑date study documentation
Create or review Transmittal Forms to ensure consistency with established standards
Develop study data specifications, including data transfer specifications, system configuration specifications, and data validation rules
Identify data errors and inconsistencies and work with project teams to drive resolution
Track outstanding data issues and follow through to resolution
Prepare and validate ad hoc data listings as required
Ensure system defects and enhancement needs are communicated to the appropriate Product Manager and that interim solutions are approved
Provide regular project status updates to the supervisor
What We Look For
Bachelor’s degree in computer science, Life Sciences, or a related field, or equivalent practical experience
At least 1 year of experience in a comparable role within the pharmaceutical, biotechnology, or CRO industry
Working knowledge of relational database structures and data validation principles
Experience using office productivity tools such as Microsoft Word, Excel, and Access
Understanding of clinical trial terminology and regulated environments
Demonstrated problem‑solving and analytical skills
Ability to work independently and collaboratively in a team environment
Strong attention to detail and organizational skills
Effective written and verbal communication skills
Ability to adapt to changing priorities while maintaining a professional and positive approach
Working Conditions
Travel: 0–15%
Lifting: Up to 25 lbs
Extended periods of computer‑based work
At Clario, our purpose is to transform lives by unlocking better evidence. It’s a cause that unites and inspires us. It’s why we come to work, and how we empower our people to make a positive impact every day. Whether you're advancing clinical science, building innovative technology, or supporting our global teams, your work helps bring life-changing therapies to patients faster.
Clario is an equal opportunity employer. Clario evaluates qualified applicants without regard to race, color, religion, gender, national origin, age, sexual orientation, gender identity or expression, protected veteran status, disability/handicap status, or any other legally protected characteristic.
Apply To This Job