Coordinate with Database Developers to ensure effective database build and timely go-live to meet the needs of the project. * Ensure the clinical database adheres to Clinical Data Acquisition ...
Coordinate with Database Developers to ensure effective database build and timely go-live to meet the needs of the project. * Ensure the clinical database adheres to Clinical Data Acquisition ...
Senior Database Engineer
Mansfield, MA · On-site +1
$112K - $152K/yr
Senior Database Engineer eClinical Solutions is transforming clinical development with elluminate, our Clinical Data Cloud, helping life sciences organizations unify, analyze, and unlock the value of ...
Senior Database Engineer
Mansfield, MA · On-site +1
$112K - $152K/yr
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Senior Database Engineer
Mansfield, MA · On-site +1
$112K - $152K/yr
Senior Database Engineer eClinical Solutions is transforming clinical development with elluminate ® , our Clinical Data Cloud, helping life sciences organizations unify, analyze, and unlock the ...
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Mansfield, MA · On-site +1
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Aliso Viejo, CA · On-site
Facilitate Data Management meetings with Clinical Operations, Project Management, Programming, Regulatory Affairs, and Study Teams. * Manage EDC study deliverables and support database management ...
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Clinical Data Manager
Aliso Viejo, CA · On-site
Facilitate Data Management meetings with Clinical Operations, Project Management, Programming, Regulatory Affairs, and Study Teams. * Manage EDC study deliverables and support database management ...
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This requires an in-depth understanding of data technology, data flow, data standards, database programming, normalization and testing. The Clinical Study Build Programmer will collaborate with Data ...
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Senior Database Engineer
Mansfield, MA · On-site
$112K - $152K/yr
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Reston, VA · On-site
Information Technology (IT), Clinical Research, Rehabilitation Therapy and Nursing. Job Title: Database Engineer Job Location: Reston VA Duration: 12 months + Responsibilities: Research and specify ...
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Our Client's Solutions group is the industry leader in clinical surveillance software that prevents ... The Database Developer will work on our Safety team and can sit in our Salt Lake City, UT office or ...
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Epic Database Administrator
Jupiter, FL · On-site +1
... and programming languages. The Epic Operational Database Administrator will use various ... of an accurate clinical database. * Creating and managing the ODB environments that serve ...
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Jupiter, FL · On-site +1
... and programming languages. The Epic Operational Database Administrator will use various ... of an accurate clinical database. * Creating and managing the ODB environments that serve ...
... and programming languages. The Epic Operational Database Administrator will use various ... of an accurate clinical database. * Creating and managing the ODB environments that serve ...
... and programming languages. The Epic Operational Database Administrator will use various ... of an accurate clinical database. * Creating and managing the ODB environments that serve ...
Experience in PL/SQL, SAS, Java, C++ relational database design and database programming skills ... Clinical Data Interchange Standards Consortium (CDISC) experience. * Travel requirements * 25 ...
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The Associate Director, Clinical Data Management is responsible for providing leadership and ... Experience in PL/SQL, SAS, Java, C++ relational database design and database programming skills ...
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Experience in PL/SQL, SAS, Java, C++ relational database design and database programming skills ... Clinical Data Interchange Standards Consortium (CDISC) experience. * Travel requirements * 25 ...
Experience in PL/SQL, SAS, Java, C++ relational database design and database programming skills ... Clinical Data Interchange Standards Consortium (CDISC) experience. * Travel requirements * 25 ...
Experience in PL/SQL, SAS, Java, C++ relational database design and database programming skills ... Clinical Data Interchange Standards Consortium (CDISC) experience. * Travel requirements * 25 ...
Experience in PL/SQL, SAS, Java, C++ relational database design and database programming skills ... Clinical Data Interchange Standards Consortium (CDISC) experience. * Travel requirements * 25 ...
The Associate Director, Clinical Data Management is responsible for providing leadership and ... Experience in PL/SQL, SAS, Java, C++ relational database design and database programming skills ...
The Associate Director, Clinical Data Management is responsible for providing leadership and ... Experience in PL/SQL, SAS, Java, C++ relational database design and database programming skills ...
Clinical Database Programmer information
See salary details
$79.4K is the 25th percentile. Wages below this are outliers.
$69.5K - $82.5K
33% of jobs
The median wage is $93.1K / yr.
$82.5K - $95.4K
21% of jobs
$95.4K - $108.4K
0% of jobs
$119.3K is the 75th percentile. Wages above this are outliers.
$108.4K - $121.3K
25% of jobs
$121.3K - $134.3K
1% of jobs
$134.3K - $147.2K
0% of jobs
$147.2K - $160.2K
0% of jobs
$160.2K - $173.1K
0% of jobs
$173.1K - $186.1K
3% of jobs
$186.1K - $199K
8% of jobs
$199K - $212K
8% of jobs
$69.5K
$119K
$212K
How much do clinical database programmer jobs pay per year?
What are the key skills and qualifications needed to thrive in the Clinical Database Programmer position, and why are they important?
To excel as a Clinical Database Programmer, you need a bachelor's degree in computer science or a related field, experience in database design, and a strong understanding of clinical data standards. Proficiency in database management systems (such as Oracle or SQL), knowledge of electronic data capture (EDC) tools like Medidata Rave, and familiarity with programming languages like SAS or SQL are commonly required, along with certifications such as CDISC or Medidata Solutions. Attention to detail, problem-solving ability, and strong communication skills are valuable soft skills for this role. Mastering these competencies is vital for ensuring high-quality, regulatory-compliant clinical trial data and effective collaboration within multidisciplinary research teams.
What is a Clinical Database Programmer job?
A Clinical Database Programmer is responsible for designing, developing, and maintaining databases used in clinical trials. They ensure that data is collected, stored, and managed efficiently while complying with regulatory standards such as CDISC and FDA guidelines. Their role involves creating database structures, writing validation checks, and supporting data analysis to ensure accurate and reliable clinical trial results. They often work with clinical data managers, biostatisticians, and regulatory teams.
What are common responsibilities and team interactions for a Clinical Database Programmer in a typical workweek?
As a Clinical Database Programmer, your primary responsibilities usually include designing, building, and validating clinical trial databases, ensuring data is collected and managed in compliance with industry standards and regulatory requirements. You will frequently collaborate with clinical data managers, biostatisticians, and study coordinators to define data collection requirements and resolve data discrepancies. Team meetings and cross-functional communication are integral parts of the role, as you work together to maintain database integrity throughout the study lifecycle. This collaborative environment provides valuable experience in both technical problem-solving and teamwork, often paving the way for advancement into senior programming or data management positions.
Full-time
Medical, Dental, Vision, Retirement, PTO
Posted 7 days ago
Altasciences rating
7.6
Based on 17 frontline employees who took The Breakroom Quiz
50th of 103 rated laboratories
Job description
Your New Company!
At Altasciences we all move in unison to assist and work in the discovery, development, and manufacturing of new drug therapies to get them faster to people who need them. No matter your role, we all play an important part and you will have a significant impact on the health and well-being of people across the globe. By living our values of Employee Development, Customer Focus, Quality and Excellence, Respect and Integrity, we look to foster a passionate and collaborative work environment and we are looking for talented and enthusiastic people, like you, to join our growing team! Whether you're a recent college graduate or seeking your next career opportunity, it's time to discover your future at Altasciences.
We are better together and together We Are Altasciences.
About The Role
The Senior Lead Data Manager is responsible for all data management activities from study start-up through database lock and archiving and independently supporting the needs of the clinical study and programs of studies. In addition, the Senior Data Manager has an active role in continuous improvement and acts as a leader in the department as demonstrated by successful mentoring and consistent study delivery over time.
What You'll Do Here
Follow department and company standard operating procedures (SOPs), forms, templates and policies. Provide feedback and update these guidelines as needed.
Act as the primary Data Management contact for the client and project team, proactively managing sponsor and interdepartmental expectations.
Develop strong client relationships that are driven by consistent study delivery in terms of quality and timeliness.
Develop, review, and maintain all study Data Management documentation.
Coordinate with Database Developers to ensure effective database build and timely go-live to meet the needs of the project.
Ensure the clinical database adheres to Clinical Data Acquisition Standards Harmonization guidelines allowing for optimal SDTM dataset programming. Suggest design for standard and non-standard data collection, identify any gaps in data collection, and challenge collection of unnecessary data.
Define electronic case report form (eCRF) and edit check specifications to support data collection and analysis required per protocol.
Take responsibility for and guide effective quality control (QC) review and user acceptance testing (UAT) of the clinical database prior to its release into production, including oversight of staff performing these tasks.
Delegate and collaborate with Data Managers on data management cleaning activities including listing review, issuing and closing queries, and external vendor data reconciliation per protocol, department and client standards, and International Conference on Harmonisation (ICH)
Good Clinical Practice (GCP) guidelines within the timelines expected by the client and project team.
Ensure data are properly reviewed in accordance with the Data Management Plan (DMP) and department and sponsor guidelines and that cleaning is effective and timely.
Track eCRFs to ensure appropriate updates and that all missing or discrepant data are queried appropriately. Monitor key study metrics and provide status reports to the sponsor and project team.
Maintain the Data Management documentation for the trial master file (TMF) according to department and Project Management processes.
Provide input on study timelines, identify risks, and communicate mitigation strategies to the Project Manager.
Provide input into improving the efficiency of data management tasks.
Lead and participate in intradepartmental or interdepartmental process and quality improvement initiatives.
Oversee direct reports as assigned.
Mentor and train other team members and/or develop training materials as needed.
What You'll Need to Succeed
Bachelor's Degree in programming, health-related sciences, or relevant field and 5-8 years of Data Management experience. Experience may be considered in lieu of education.
Excellent verbal and written communication skills.
Professional attitude and strong interpersonal skills.
Ability to work well with a multi-disciplinary team of professionals.
Client-focused approach to work.
Flexible attitude with respect to work assignments and new learning.
Ability to prioritize workload.
Superior attention to detail.
Understanding of clinical research and the relationship of Data Management in the clinical study process.
Proven history of continuous improvement.
Strong technical aptitude and ability to adapt to multiple data management platforms.
Strong knowledge of electronic data capture (EDC) clinical data management systems.
Good computer skills (Microsoft Word, Excel, and Power Point) and ability to understand and adapt to various information technology (IT) systems.
Altasciences strives to provide a French working environment for its employees in Quebec. Although as part of its francization program has taken all reasonable steps to avoid imposing the above-mentioned requirement. Fluency in English is an essential requirement for the position of Senior Lead Data Manager including, but not limited to, for the following reasons:
The requirement to have study protocols, designs and clinical research documents written and documented in English as required by industry regulatory agencies.
The employee communicates frequently with Altasciences employees across Canada and the United States. As such, English is the main language used to correspond between offices.
What We Offer
The payrange estimated for this position is $65,660 - $87,548. Please note that salaries vary within the range based on factorsincluding, but not limited to, prior relevant experience, skills, education,certification, location as well as internal equity and market data.
Altasciences' Benefits Package Includes:
Health/Dental/Vision Insurance Plans
401(k)/RRSP with Employer Match
Paid Vacation and Holidays
Paid Sick and Bereavement Leave
Employee Assistance & TelehealthPrograms
Altasciences' Incentive Programs Include:
Training & Development Programs
Employee Referral BonusProgram
Annual Performance Review
#LI-TN1
MOVING IN UNISON TO DELIVER A BIG IMPACT WITH A PERSONAL TOUCH
Altasciences is an equal opportunity employer committed to diversity and inclusion. Our goal is to attract, develop and retain highly talented employees from diverse backgrounds, allowing us to benefit from a wide variety of experiences and perspectives. All qualified applicants will receive consideration for employment without regard to age, race, color, religion, creed, sex, sexual orientation, gender identity, national origin, disability or any other protected grounds under applicable legislation. Reasonable accommodations for persons with disabilities during the recruitment process are available upon request. Join us at Altasciences!
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