Associate Director, Clinical Data Management - CDISC
Corcept Therapeutics
Corcept Therapeutics is seeking an Associate Director, Clinical Data Management in Redwood City, CA to optimize data collection, flow, and access across EDC and non-EDC sources. You will ensure CDISC compliance, data quality, and timely delivery of clinical data for trials. The role demands 10+ years in clinical data management, strong leadership, and hands-on experience with CDISC standards, EDC systems, and data visualization tools. HQ-based position with competitive salary. #J-18808-Ljbffr Corcept Therapeutics
$229.3k - $269.8k
...cortisol modulation. Explore our current job opportunities. Associate Director, Clinical Data Management Redwood City, California, United States For more than... ...sources. Responsible for accuracy, completeness and CDISC compliance of Corcept clinical databases....SuggestedFull time$186k - $233k
Revolution Medicines is a late-stage clinical oncology company developing novel... ...position has a key role in the day-to-day management of Clinical Data Management (CDM) activities.... ...CDM in Clinical Team meetings. The Associate Director, Clinical Data Management, will be...SuggestedFull timeLocal areaOverseas$155k - $190k
...Associate Director, Clinical Data Systems And Informatics Location: San Mateo, CA; San Diego, CA ClearNote... ...of our diagnostic tests through management of clinical data flow into our data... ...of clinical data standards (CDASH/CDISC preferred) ~ Familiarity with query...Suggested$174k - $204k
Associate Director, Clinical Data Management About Summit: Summit Therapeutics Inc. is a biopharmaceutical oncology company with a mission focused on improving quality of life, increasing potential duration of life, and resolving serious unmet medical needs. At Summit...SuggestedContract workFor contractorsFor subcontractorWork at office- Summit Therapeutics is seeking an Associate Director of Clinical Data Management to lead data management across global oncology trials, ensure high data quality, integrity, and timely delivery. You will collaborate with Clinical Operations, Biostatistics, Regulatory, and...Suggested
$186k - $233k
Revolution Medicines is a late-stage clinical oncology company developing... ...Medicines is seeking an Associate Director, Clinical Quality Assurance,... ...enable risk-based quality management and a culture of quality and... ...and security of personal data very seriously and respects...Full timeLocal area- Revolution Medicines, a late-stage oncology company in Redwood City, seeks an Associate Director of Clinical Data Management to lead day-to-day CDM activities across trials, ensure data accuracy, and coordinate with CROs and vendors. The role focuses on developing data...
$186k - $233k
...Revolution Medicines is a late-stage clinical oncology company developing... ...activities. The Associate Director will collaborate across functions... ...leadership Lead and manage biostatistical activities to... ...quality. Collaborate with data management and clinical operations...Full timeLocal area- Corcept Therapeutics in Redwood City, CA is seeking an Associate Director of Clinical Quality Assurance to lead day-to-day CQA operations across clinical programs and ensure regulatory compliance for Corcept's studies. This hybrid role requires on-site presence three days...3 days per week
$186k - $233k
...Revolution Medicines is a late-stage clinical oncology company developing... ....The Opportunity:As an Associate Director, you will be responsible for... ...with clinical study management, International Conference on... ...protection and security of personal data very seriously and respects...Full timeWork at officeLocal area$186k - $233k
Revolution Medicines is a late-stage clinical oncology company developing novel targeted therapies... ...lead for assigned program(s) and develop/manage the clinical supply plan.Plan and deliver... ...protection and security of personal data very seriously and respects your right to...Full timeLocal area$192.7k - $226.7k
...glucocorticoid receptor antagonists. With advanced clinical trials in patients with... ...California. To learn more, visit The Associate Director of Clinical Quality Assurance (CQA) is... ...clinical development program Support the management and growth of the CQA team with the...Full timeWork at office3 days per week- Position: Associate Director / Senior Manager, Clinical Development Program Manager Location: Redwood City, CA Job Id: 264-1150 # of Openings: 1 Associate Director / Senior Manager, Clinical Development Program Manager Allakos Inc. is a clinical-stage company developing...
$50 - $60 per hour
Principal Scientist/Associate Director, Clinical Biomarkers Principal Scientist/Associate Director, Clinical... ...assays to translate preclinical data into clinical biomarkers for advancing... ..., communication, and project management skills, with the ability to anticipate...Full timeRelocation package- Revolution Medicines in Redwood City, CA is seeking a skilled Clinical Supply Lead to plan and deliver clinical materials for multiple programs. You will manage forecasting, labeling, packaging, distribution, and inventory, ensuring compliance with development plans. The...
$210.38k - $272.25k
...WorkWorks as part of a team responsible for managing contractors, technical delivery partners,... ...model development, application patterns, data pipelines, and production AI systems.... ...capabilities supporting research, development, clinical, regulatory, safety, and enterprise use...Full timeFor contractorsLocal area$186k - $233k
Revolution Medicines is a late-stage clinical oncology company developing... ...therapies to patients. The Associate Director, Environmental Health &... ...actions.Oversee incident management processes, including investigation... ...and security of personal data very seriously and respects...Full timeLocal areaFlexible hours- ...Job TitleResponsibilities:Collaborate with data managers, statistical programmers, biostatistics, clinical operations, and external vendors to review, sign off on... ...experience using CRF-Annotation, FDA regulations such as CDISC, 21 CFR Part 11, ICH, GCP guidelines, and other...Work experience placement
$255k - $265k
...a dynamic workplace for employees to grow and develop their skills.The Associate Medical Director is involved in the design, safety monitoring, and data analysis of the Company’s late-phase clinical trials in endocrinology. As such, the Associate Medical Director is an...Full timeTemporary workFlexible hours- ...generations to come.POSITION OVERVIEW: Clinical Operations is responsible for the worldwide... ...timely and high-quality clinical data that supports global registration and commercialization... ...will be responsible for the resource management of multiple studies within a program or...Full timeContract workFor contractorsLocal areaWorldwide
- A global biopharma company in Palo Alto is seeking an Associate Director, AI Data Scientist to lead the implementation of AI and ML solutions in clinical trial execution and digital healthcare. The ideal candidate will have strong programming skills in Python, and experience...
$185k - $205k
Position: Associate Director, Clinical Operations Location: Newark, CAJob Id: 398 # of Openings:... ...Phase 1-3 global clinical trials. Experience leading a team managing international trials using CROs from set-up through to...Worldwide$166k - $230k
Join to apply for the SR.MANAGER, CLINICAL DATA MANAGEMENT role at BioSpace 2... ...Guidelines, DTSs, etc. Knowledge of CDISC Standard including CDASH... ...Deep expertise in CDM and associated technologies, processes and... ...00.00 3 days ago Associate Director, Clinical Data Management...Full timeContract workTemporary workWork at officeFlexible hours3 days per week$186k - $233k
...Medicines is a late-stage clinical oncology company... ...ensuring conformance to CDISC standards and submission... ...audits.Timeline and vendor management for deliverables,... ...datasets (SDTM, ADaM) and data documentation, Reviewer... ...Committee meetings, Board of Director meetings, Exploratory...Full timeFor contractorsLocal area- Ascendis Pharma is seeking an Associate Medical Director to lead late-phase clinical trials in endocrinology. This role involves overseeing clinical trial design and ensuring compliance with trial protocols. The ideal candidate will possess an M.D. degree, board certification...
$229.3k - $269.8k
...antagonists. With advanced clinical trials in patients with hypercortisolism... ...learn more, visit As an Associate Medical Director, you will support the... ...clinical protocols, data collection systems and final... ...finance Participate in the management of human resources in a matrixed...Full time$183.5k - $269.8k
...antagonists. With advanced clinical trials in patients with... ...learn more, visit The Associate Director of Biostatistics will be responsible... .... This position will manage external statisticians and... ...in the evaluation of CDISC electronic data packages for completeness,...Full timeFor contractors3 days per week$229.3k - $269.8k
...antagonists. With advanced clinical trials in patients with... ...Statistical Programming team, the Associate Director is responsible for the... ...readiness of study data packages per CDISC standards and FDA guidance... ...: Work with data management to review CRO generated...Full time- A leading biotech company in Redwood City is seeking an Associate Director/Senior Manager, Clinical Development Program Manager. The role involves driving clinical development programs, collaborating with senior stakeholders, and managing project plans to maximize program...
- ...patients worldwide. Please visit for more information. The Associate Director, AI Data Scientist will be responsible for leading the... ...transformative AI/ML/GenAI solutions across the areas of Clinical Trial Execution and Digital Healthcare across Jazz Research...Work at officeWorldwideFlexible hours
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