Manager, Data Management
Durham, NC · On-site
Take a leadership role to gather content and integration requirements for EDC and close collaboration with partners supporting other data collection systems (Non-EDC Data) * Represent DM on cross ...
62 Edc Data Jobs Hiring Near You
Manager, Data Management
Durham, NC · On-site
Take a leadership role to gather content and integration requirements for EDC and close collaboration with partners supporting other data collection systems (Non-EDC Data) * Represent DM on cross ...
EDC Developer / Programmer
OR · Remote
We are looking for a performance-oriented, innovative and self-motivated team player to join our Clinical Data Sciences team as a full-time Electronic Data Capture (EDC) Database Developer / Clinical ...
Quick apply
EDC Developer / Programmer
OR · Remote
We are looking for a performance-oriented, innovative and self-motivated team player to join our Clinical Data Sciences team as a full-time Electronic Data Capture (EDC) Database Developer / Clinical ...
Take a leadership role to gather content and integration requirements for EDC and close collaboration with partners supporting other data collection systems (Non-EDC Data) * Represent DM on cross ...
Take a leadership role to gather content and integration requirements for EDC and close collaboration with partners supporting other data collection systems (Non-EDC Data) * Represent DM on cross ...
Manager, Data Management
Durham, NC · On-site
Take a leadership role to gather content and integration requirements for EDC and close collaboration with partners supporting other data collection systems (Non-EDC Data) * Represent DM on cross ...
Manager, Data Management
Durham, NC · On-site
Take a leadership role to gather content and integration requirements for EDC and close collaboration with partners supporting other data collection systems (Non-EDC Data) * Represent DM on cross ...
Take a leadership role to gather content and integration requirements for EDC and close collaboration with partners supporting other data collection systems (Non-EDC Data) * Represent DM on cross ...
Take a leadership role to gather content and integration requirements for EDC and close collaboration with partners supporting other data collection systems (Non-EDC Data) * Represent DM on cross ...
Contribute to the implementation and optimization of clinical data systems and tools (e.g., EDC, data review platforms). Education / Qualifications * Bachelor's degree in Life Sciences, Data Science ...
Contribute to the implementation and optimization of clinical data systems and tools (e.g., EDC, data review platforms). Education / Qualifications * Bachelor's degree in Life Sciences, Data Science ...
Contribute to the implementation and optimization of clinical data systems and tools (e.g., EDC, data review platforms). Education / Qualifications * Bachelor's degree in Life Sciences, Data Science ...
Contribute to the implementation and optimization of clinical data systems and tools (e.g., EDC, data review platforms). Education / Qualifications * Bachelor's degree in Life Sciences, Data Science ...
Defining and driving the strategy for collecting clinical trial data, including site based (EDC) data, external vendor data, eCOA data, and other device/digital data, integrating with end-to-end data ...
Defining and driving the strategy for collecting clinical trial data, including site based (EDC) data, external vendor data, eCOA data, and other device/digital data, integrating with end-to-end data ...
We are looking for a performance-oriented, innovative and self-motivated team player to join our Clinical Data Sciences team as a full-time Electronic Data Capture (EDC) Database Developer / Clinical ...
We are looking for a performance-oriented, innovative and self-motivated team player to join our Clinical Data Sciences team as a full-time Electronic Data Capture (EDC) Database Developer / Clinical ...
Defining and driving the strategy for collecting clinical trial data, including site based (EDC) data, external vendor data, eCOA data, and other device/digital data, integrating with end-to-end data ...
Defining and driving the strategy for collecting clinical trial data, including site based (EDC) data, external vendor data, eCOA data, and other device/digital data, integrating with end-to-end data ...
We are looking for a performance-oriented, innovative and self-motivated team player to join our Clinical Data Sciences team as a full-time Electronic Data Capture (EDC) Database Developer / Clinical ...
We are looking for a performance-oriented, innovative and self-motivated team player to join our Clinical Data Sciences team as a full-time Electronic Data Capture (EDC) Database Developer / Clinical ...
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Clinical Research Coordinator (CRC)
Flower Mound, TX · On-site
$50K - $70K/yr
Maintain high-quality source documentation and EDC data entry (real-time, audit-ready) * Manage investigational product accountability and study logistics * Serve as the primary point of contact for ...
Quick apply
Be Seen First
Clinical Research Coordinator (CRC)
Flower Mound, TX · On-site
$50K - $70K/yr
Maintain high-quality source documentation and EDC data entry (real-time, audit-ready) * Manage investigational product accountability and study logistics * Serve as the primary point of contact for ...
Defining and driving the strategy for collecting clinical trial data, including site based (EDC) data, external vendor data, eCOA data, and other device/digital data, integrating with end-to-end data ...
Defining and driving the strategy for collecting clinical trial data, including site based (EDC) data, external vendor data, eCOA data, and other device/digital data, integrating with end-to-end data ...
Defining and driving the strategy for collecting clinical trial data, including site based (EDC) data, external vendor data, eCOA data, and other device/digital data, integrating with end-to-end data ...
Defining and driving the strategy for collecting clinical trial data, including site based (EDC) data, external vendor data, eCOA data, and other device/digital data, integrating with end-to-end data ...
Contribute to the implementation and optimization of clinical data systems and tools (e.g., EDC, data review platforms). Education / Qualifications * Bachelor's degree in Life Sciences, Data Science ...
Quick apply
Contribute to the implementation and optimization of clinical data systems and tools (e.g., EDC, data review platforms). Education / Qualifications * Bachelor's degree in Life Sciences, Data Science ...
Role: eCOA / eDC Clinical Data Programmer Role Responsibilities * Gather and influence eCOA design specifications to enable successful clinical trial implementation. * Program and test data ...
Role: eCOA / eDC Clinical Data Programmer Role Responsibilities * Gather and influence eCOA design specifications to enable successful clinical trial implementation. * Program and test data ...
Role: eCOA / eDC Clinical Data Programmer Role Responsibilities * Gather and influence eCOA design specifications to enable successful clinical trial implementation. * Program and test data ...
Role: eCOA / eDC Clinical Data Programmer Role Responsibilities * Gather and influence eCOA design specifications to enable successful clinical trial implementation. * Program and test data ...
This position provides support for the EDC data center infrastructure services including Windows and Linux server administration, Active Directory services, Public Key Infrastructure (PKI ...
This position provides support for the EDC data center infrastructure services including Windows and Linux server administration, Active Directory services, Public Key Infrastructure (PKI ...
Experience working with EDC data, Lab imaging data and external vendor data. * Collaborate with Biostatistics, Data Management, and Clinical Operations to support data cleaning, reconciliation, and ...
Experience working with EDC data, Lab imaging data and external vendor data. * Collaborate with Biostatistics, Data Management, and Clinical Operations to support data cleaning, reconciliation, and ...
Director, Clinical Data Management
Warren, NJ · On-site
$201 - $253/hr
This position has a leadership role to proactively develop plans for the utilization of EDC system processes and other clinical data applications that allow for internal control of clinical databases.
Director, Clinical Data Management
Warren, NJ · On-site
$201 - $253/hr
This position has a leadership role to proactively develop plans for the utilization of EDC system processes and other clinical data applications that allow for internal control of clinical databases.
EDC Jobs Information
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Full-time
Posted 7 days ago
Job description
Opportunity for Secondment to AskBio
We're pleased to share an exciting secondment opportunity at AskBio.
This role is available for a time period to be determined by leadership at both Bayer and AskBio. While most assignments range from one to two years, the exact duration will be based on business needs and mutual agreement.
This secondment offers a unique chance to broaden your experience, expand your knowledge, and contribute meaningfully to AskBio's mission: to advance gene therapy and change the lives of patients around the world.
If you're interested in exploring this opportunity, we encourage you to:
We look forward to seeing how our colleagues continue to grow and make an impact across the Bayer-AskBio partnership.
Our vision: Pioneering science to create transformative molecular medicines.
Our mission: Lead innovative science and drive clinical outcomes to transform people's lives.
Our principles:
Our values:
Position Summary
We have an opportunity for Manager, Clinical Data Management to join the AskBio team in our RTP, North Carolina, location and be part of our continued success!
The Manager, Clinical Data Management, provides oversight of all data management activities outsourced to external suppliers and/or conducted in-house, from study set-up, to conduct and close out. including but not limited to database design specification development, database design programming, database User Acceptance Testing (UAT), database deployment to research sites, data review and database lock and data archiving. Therefore, ensure the quality and integrity of all databases used in AskBio sponsored trials.
This position will report to the Senior Director, Data Management.
Job Responsibilities
Minimum Requirements
Preferred Education, Experience and Skills
AskBio Inc. (AskBio) is an Equal Opportunity Employer and does not discriminate against any employee or applicant for employment because of race, color, religion, gender, sexual orientation, gender identity, national origin, age, disability, veteran status or any other protected status prohibited under Federal, State or local laws. All employment decisions are based on valid job-related requirements. If you are a qualified individual with a disability or a disabled veteran and are unable or limited in your ability to use or access our website, you may request a reasonable accommodation to express interest in a specific opening by calling us at (919) 561-6210 or sending us an email at talent@askbio.com.
We're pleased to share an exciting secondment opportunity at AskBio.
This role is available for a time period to be determined by leadership at both Bayer and AskBio. While most assignments range from one to two years, the exact duration will be based on business needs and mutual agreement.
This secondment offers a unique chance to broaden your experience, expand your knowledge, and contribute meaningfully to AskBio's mission: to advance gene therapy and change the lives of patients around the world.
If you're interested in exploring this opportunity, we encourage you to:
- Speak with your direct manager to discuss your interest and alignment with your development goals.
- Apply directly using the link provided in the posting.
We look forward to seeing how our colleagues continue to grow and make an impact across the Bayer-AskBio partnership.
Our vision: Pioneering science to create transformative molecular medicines.
Our mission: Lead innovative science and drive clinical outcomes to transform people's lives.
Our principles:
- Advance innovative science by pushing boundaries.
- Bring transformative therapeutics to patients in need.
- Provide an environment for employees to reach their fullest potential.
Our values:
- Be a Pioneer. We are not afraid of the impossible and to innovate to make gene therapies accessible to those in need.
- Cultivate Collaboration. Strive to be the best teammate, actively listen, openly communicate, and embrace diverse points of view.
- Embrace Responsibility. We are humbled by the enormity of our mission. We hold a relentless commitment to advance science and clinical outcomes for our patients, families, and caregivers.
- Raise the Bar. Continuously drive improvements and efficiencies. Seek and provide constructive feedback. Have a bias for learning and action.
- Act with Uncompromising Integrity. Be honest, transparent, and committed to doing what's right in every situation. Make clear commitments and follow through.
Position Summary
We have an opportunity for Manager, Clinical Data Management to join the AskBio team in our RTP, North Carolina, location and be part of our continued success!
The Manager, Clinical Data Management, provides oversight of all data management activities outsourced to external suppliers and/or conducted in-house, from study set-up, to conduct and close out. including but not limited to database design specification development, database design programming, database User Acceptance Testing (UAT), database deployment to research sites, data review and database lock and data archiving. Therefore, ensure the quality and integrity of all databases used in AskBio sponsored trials.
This position will report to the Senior Director, Data Management.
Job Responsibilities
- Ensure that end-to-end Data Management activities are conducted in accordance with high ethical and quality standards, all applicable GCP regulations and company procedures
- Provide oversight of all data management activities outsourced to external suppliers and/or conducted in-house, including but not limited to Data Management Plan, database specification development, database design programming, database User Acceptance Testing (UAT), database deployment to research sites, data review, coding and database locks
- Efficiently plan, coordinate, and deliver complete, high quality and reliable clinical trial data in a timely manner for assigned projects
- Serve as the DM point of contact for internal and external study team members with minimal oversight from senior data management resources
- Provide strong quality and project oversight over third-party vendor responsible for data management deliverables
- Take a leadership role to gather content and integration requirements for EDC and close collaboration with partners supporting other data collection systems (Non-EDC Data)
- Represent DM on cross-functional project teams & submission teams
- Provide support for Health Authority inspections and audits
- Effectively manage changes to database design and data management requirements as necessary due to protocol amendments and changes to overall clinical development programs
- Develop, troubleshoot, and maintain complex programs and utilities leading to database design, creation, validation, & use as well as clinical trial statistical analysis
- Participate in the development of departmental standard operating procedures, working procedures and guidance documents
Minimum Requirements
- Bachelor's degree in life sciences, statistics, biostatistics, mathematics, computer science, biotechnology or related field with a minimum of 6 years' clinical trial related data management experience
- Prior use of and/or familiarity with clinical trial database packages such as Veeva EDC, Medidata Rave
- Significant knowledge of the drug development process, clinical trial methodology, data management & statistics and relevant regulatory requirements for drug approval
- Demonstrated ability to operate and lead in a matrix organization, building successful working relationships and effective stakeholder management in an environment that requires diverse educational and functional expertise
Preferred Education, Experience and Skills
- Good knowledge of CDASH® standards and how they support CDISC® standards (SDTM). Hands on experience of confirming database design and DM principles are consistent with all types CDASH® of and their support of SDTM
- Experience managing multiple sources of data
- Experience identifying and mitigating potential risks in the DM space; problem resolution skills to solve errors/inconsistencies found in data processing to reduce risk to data integrity and validity
- Experience in managing gene therapy studies
- Excellent verbal and written communications skills; able to communicate proactively and effectively
- Utilizing and developing SAS, SQL, Power BI, Excel and other analytical tools to support clinical data review, identifying data trends and discrepancies, and monitoring study performance metrics
AskBio Inc. (AskBio) is an Equal Opportunity Employer and does not discriminate against any employee or applicant for employment because of race, color, religion, gender, sexual orientation, gender identity, national origin, age, disability, veteran status or any other protected status prohibited under Federal, State or local laws. All employment decisions are based on valid job-related requirements. If you are a qualified individual with a disability or a disabled veteran and are unable or limited in your ability to use or access our website, you may request a reasonable accommodation to express interest in a specific opening by calling us at (919) 561-6210 or sending us an email at talent@askbio.com.