Senior Clinical Database Programmer
Katalyst HealthCares & Life Sciences
Job-ID32188454Reference26-00482 Job Description: Design, build, and configure clinical study databases in EDC/CDM platforms. Ensure systems meet client needs, follow GCDMP, support accurate data capture, workflows, edit checks, and integrations. Responsibilities: Lead Study Build / Database Configuration in EDC systems. Configure Edit Checks, Workflows, Validations. Gather & translate client requirements into solutions. Create Specifications / Test Cases / UAT Support. Support integrations & data transfers with vendors. Deliver client workshops (remote/on-site). Manage timelines, budgets & project deliverables. Resolve implementation / configuration issues. Provide status reports to stakeholders. Mentor junior team members / train new hires. Drive process improvements & best practices. Ensure SOP / compliance adherence. Requirements: Strong knowledge of Clinical Trial Processes. Hands-on experience with Medidata Rave, Oracle Clinical, OpenClinica. Study database build & configuration expertise. Understanding of CDISC / Data Standards / Data Management. UAT, QC Testing, Functional Documentation. Integrations / Data Migration knowledge. Strong analytical & problem-solving skills. Excellent communication & stakeholder management. Team leadership / mentoring experience.
- ...leadership, strategic planning, direction and implementation of clinical systems for data collection which may include vendor selection,... ...development, validation, and management of the clinical study database throughout its life cycle, from CRF design, database development...SeniorRemote work
$129.5k - $163.1k
...Site: Job Description Summary: The Senior Manager, Clinical Data Management is responsible for... ...accuracy and consistency of clinical databases for subsequent analysis and reporting... ...Operations group, biostatisticians, SAS programmers and other staff as appropriate to...SeniorTemporary workWork experience placementWork at office$90k - $130k
...Everest Clinical Research (“Everest”) is a full-service contract research... ...to join our winning team as Senior Clinical Data Managers for... ...is responsible for providing database and data management... ...Plan (DQRP). Coordinate with programmers to complete the programming and...SeniorContract workTemporary workWork at officeRemote workWork from homeWorldwide- ...PTC Therapeutics seeks a Senior Manager of Clinical Data Management to oversee data integrity and database development for clinical trials. The role involves managing data collection processes, collaborating with internal teams and external vendors, and ensuring regulatory...SeniorWork at office
$70.5k - $96.91k
...and education programs that drive clear economic value, better clinical outcomes and improved quality of life for patients. TMC is part... ...activities: protocol review, CRF design and development, development of database specifications, development of edit check specifications,...SuggestedTemporary workWork at officeWorldwide$173.2k - $272.6k
...Job Description The Senior Director, Data Collection Data Steward serves on the GCDS... ...aligned with industry standards (e.g., CDISC [Clinical Data Interchange Standards Consortium])... ...Case Report Form) design, clinical database development and validation, user acceptance...SeniorFull timeFor contractorsLocal areaWorldwideRelocationVisa sponsorshipFlexible hoursShift work- Katalyst CRO is seeking a senior CDM leader to drive clinical data management across studies. You will oversee CRF design, data validation plans, and eCRF testing, while coordinating with vendors and cross-functional partners to meet regulatory standards. Ideal candidates...Senior
- Merck & Co., Rahway, NJ, seeks a Senior Director/Sr. Principal Scientist in Oncology to lead planning and execution of clinical development for oncology medicines from pre-clinical to post-licensure. You will design studies, monitor trials, and manage regulatory reporting...Senior
- The Data Sharing Manager serves as a subject matter expert in clinical data sharing, operating independently to manage and oversee the... ..., Coaching, Critical Thinking, Cross-Functional Collaboration, Database Management, Data Governance, Data Management, Data Privacy Standards...Flexible hours
- Rutgers University seeks a Biostatistician III to lead statistical activities for clinical and translational research. You will independently design analyses, coordinate programming, and collaborate with investigators, sponsors, data managers, and regulatory experts under...Senior
- Scorpion Therapeutics seeks a Principal C&SP Methodology Lead to oversee technical programming development and innovation within clinical and statistical data sciences for biopharma. You will guide departmental strategies, drive automation, and support global implementation...SeniorRemote job
$282.2k
...talented and dedicated colleagues while developing and expanding your career. The Senior Director (Sr. Principal Scientist) has primary responsibility for the planning and directing clinical research activities involving new or marketed Oncology medicines. Our Company's...SeniorFull timeFor contractorsLocal areaFlexible hours$1,000 per day
Comprehensive Mobile Care (CMC) is seeking a Part-Time Optometrist (OD) to provide outpatient eye care in a clinic-based setting serving seniors. This 1099 independent contractor role offers schedule flexibility with on-site work in Central New Jersey, 5-6 days per month...SeniorPart timeFor contractorsWeekend work- ...life-cycle of the study protocol, which includes CRF annotation, database specifications, edit checks and other pertinent data management... ...to evaluate efficiency, accuracy, and speed in cleaning clinical study data and locking database for study reporting -Ensure data...Interim roleImmediate start
$92.32k - $126.94k
...and education programs that drive clear economic value, better clinical outcomes and improved quality of life for patients. TMC is... ...trial management systems; willingness to learn new systems / databases as needed. Qualifications/ Background ExperiencesBS / BA or higher...SeniorTemporary workWork experience placementInterim roleWorldwide$75k - $125k
...About Vitalief Vitalief is a consulting and professional services firm that helps clinical research sites, sponsors, and CROs improve trial activation, operational performance, and workforce readiness. Our approach combines clinical research expertise, operational...SeniorFull timeRemote workFlexible hours$282.2k
...talented and dedicated colleagues while developing and expanding your career.- The Senior Director (Sr. Principal Scientist) has primary responsibility for the planning and directing clinical research activities involving new or marketed Oncology medicines. Our Company's...SeniorFull timeFor contractorsLocal areaRelocationVisa sponsorshipFlexible hoursShift work$280.35k
...society", we are shaping a healthier, more hopeful future for patients, their families, and society.Job SummaryThe Sr. Director, Clinical Safety, will lead the development and implementation of integrated project/product risk management strategies aimed at achieving the...Senior$173.2k - $272.6k
...Senior Director leading Merck's Global Clinical Data Standards team to establish governance frameworks, oversee data collection standards aligned with industry regulations, and manage strategic initiatives across clinical development. Reports to leadership, manages teams...SeniorWorldwide$280.35k
...", we are shaping a healthier, more hopeful future for patients, their families, and society.Job SummaryThe Senior Director sits within Global Oncology Clinical Development, an organization dedicated to the effective strategy, design, execution, and interpretation of Oncology...Senior$140k - $174k
...culture that inspires our people to achieve common goals. Together, let's build a brighter, healthier future for all.Role SummaryThe Senior Manager, Data Delivery - Global Skin Health is a pivotal role dedicated to building and scaling the core data foundation that fuels...SeniorHourly payWork at officeLocal areaRemote workRelocation$180k - $210k
Everest Clinical Research (“Everest”) is a full-service contract research organization (CRO) providing a broad range of expertise-based... ...data operations to provide complete, valid, safe, and secure databases which meet corporate and regulatory clinical data requirements...Contract workWork at officeLocal areaRemote workWork from homeWorldwide- Everest Clinical Research seeks a Director, Clinical Data Management for our Bridgewater, New Jersey on-site location, or remotely from... ...data operations to deliver complete, valid, and secure databases, while managing budgets, resources, and client projects; ensuring...Remote jobWork at officeWork from home
- Merck is seeking a Clinical Data Manager (CDM) to execute end-to-end data management activities for clinical trials, including data collection, validation, query management, medical coding, and database lock preparation, per SOPs and ICH-GCP guidelines. You will support...
- Primary & Secondary Skill: SDTM/Clinical SAS 1.Must have 6-8 yrs of exp in clinical domain 2.Strong knowledge of SDTM 3.Create advanced SAS macros, templates, and utilities for efficient data processing 4.Act as the primary programming point of contact for biostatisticians...Senior
- Merck & Co. in Rahway, NJ is seeking a senior clinical operations leader to oversee the planning and execution of one or more clinical trials. You will lead cross-functional teams, apply project management skills, and ensure adherence to GCP/ICH standards in a global context...Senior
$280.35k
...of society", we are shaping a healthier, more hopeful future for patients, their families, and society.Job SummaryThe Senior Director, Early Clinical Development role oversees early-stage oncology trials, such as global clinical development program for multiple product...Senior- Merck & Co. is seeking an experienced Clinical Systems Implementation Team Lead to oversee validation, implementation, and adoption of clinical trial applications. You will manage a team, partner with IT and business stakeholders, and ensure SDLC compliance. Responsibilities...Senior
- A leading global pharmaceutical company is seeking a Senior Director of Clinical Safety to lead risk management strategies for development compounds. This role requires strong leadership and collaboration with cross-functional teams. The ideal candidate should have an MD...Senior
- MSD is seeking a Senior Director, Clinical Science, GI Oncology to lead strategic Clinical Science across GI cancers. You will shape study design, data interpretation, and scientific standards while partnering with cross-functional teams to drive development plans and portfolio...Senior
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