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.
- ...Job Description Job Description Job Description: The Senior RAVE Clinical Database Programmer participates in the design, development, validation, and maintenance of clinical study databases. This individual applies advanced knowledge of CRF design, database configuration...Senior
- ...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- ...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- 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
- 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
$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- ...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$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$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$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
...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$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- ...Senior Clinical Trial Manager / Clinical Operations Lead Are you an experienced Clinical Trial Manager with a strong background in global... ...with Data Management and clinical teams to support database lock and data review milestones Maintain strong inspection...SeniorFull time
$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$70k - $80k
...intersection of Sites, Sponsors, and CROs across the research and clinical trials landscape. By blending deep subject matter expertise... ...benefit patients. We are seeking a talented and enthusiastic Senior Clinical Research Coordinator to join our exceptional team (as...SeniorFull timeTemporary workWork at officeRemote work- Merck & Co., Inc. in Rahway, NJ is seeking a senior Clinical Trial Operations leader to drive strategy and execution of one or more clinical trials within a global, cross-functional team. You will coach and develop teams, oversee study planning, execution, governance, and...Senior
- Merck & Co., Inc. in Rahway, NJ seeks an experienced Clinical and Regulatory Medical Writer to prepare regulatory and public-facing documents in alignment with regulatory requirements and health-literacy standards. You will lead cross-functional teams, manage multiple...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- A leading medical media company in Cranbury Township is seeking a Senior Clinical Content Producer to lead content strategies and build expert relationships. The role demands a creative storyteller with strong scientific acumen and on-camera confidence. Ideal candidates...Senior
$282.2k
...Senior Principal Scientist position leading clinical research strategy and execution for oncology drugs across all development phases. Responsible for study design, trial management, regulatory submissions, and cross-functional collaboration within a global healthcare...Senior- Merck & Co., Inc. in Rahway, NJ, USA, seeks an experienced CRA to oversee clinical study sites, ensure protocol compliance, and lead monitoring activities across multiple sites. You will work under CRA-Manager oversight to maintain data integrity and regulatory compliance...SeniorRemote job
$282.2k
...Senior Principal Scientist position in breast cancer clinical research at a pharmaceutical company. Responsibilities include developing clinical trial strategies, evaluating preclinical data, managing ongoing studies, and collaborating across functional teams to advance...Senior$282.2k
Job DescriptionThe Senior Director (Sr. Principal Scientist) has primary responsibility for the planning and directing clinical research activities involving new or marketed medicines in the Metabolism section of the Atherosclerosis & Metabolism therapeutic area, with...SeniorFull timeFor contractorsLocal areaFlexible hours$170k - $190k
The Senior Clinical Trial Drug Supply Manager is a critical position within the clinical development organization directly supporting the execution of clinical trials and regulatory submissions. This role will be responsible for multiple global studies and the independent...SeniorTemporary workWork at officeFlexible hours- ...Data Steward, Global Data Management and Standards (GDMS), Global Clinical Data Standards (GCDS) provides program-level oversight of data... ...electronic eCRF (electronic Case Report Form) design, clinical database development and validation, user acceptance testing, external...Full timeWorldwide
$285k - $315k
...Job Title Senior Director, Clinical Development Requisition JR000015848 Senior Director, Clinical Development (Open) Location... ...and Monitoring Plans, Clinical Data Review Plan, Clinical Database specifications, statistical analysis plan, the data management...SeniorWork at officeFlexible hours
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