Clinical Data AMS Sr. Consultant
$120.2k - $140kDeloitte
Position Summary Are you an experienced, passionate pioneer in technology who wants to work in a collaborative environment? As an experienced Clinical Data AMS Senior Consultant you will have the ability to share new ideas and collaborate on projects as a consultant without the extensive demands of travel. If so, consider an opportunity with Deloitte under our Project Talent Model. Project Talent Model (PTM) is a talent model that is tailored specifically for long-term, remote client service delivery. Recruiting for this role ends on 10/1/2026 Position Summary The Clinical Data Analytics (CDA) AMS Lead will serve as the primary functional and operational expert for the Clinical Data Analytics (CDA) technology portfolio, with primary emphasis on SAS Grid Administration supporting biostatistics and real-world data (RWD) science operations. This role owns the health, stability, and compliance posture of a suite of clinical and regulatory R&D platforms — including Axway Secure Transport (ST), eClinical Elluminate, Eclipse (medical coding), and EAST — across the full engagement lifecycle: implementation, configuration, validation, and steady-state managed services. The AMS Lead acts as the escalation point for platform issues, drives root-cause resolution, and ensures all supported systems remain inspection-ready in accordance with global regulatory standards (GxP, 21 CFR Part 11, GDPR/HIPAA as applicable). Work you’ll do/Responsibilities As a Clinical Data AMS Senior Consultant, you will provide own day-to-day administration, monitoring, patching, upgrades, troubleshooting and performance tuning of the SAS Grid environment (grid nodes, metadata server, workspace/stored process servers), ensuring high availability for biostatistical programming and RWE workloads. Manage configuration, patching, upgrades, and troubleshooting for Axway Secure Transport (ST), ensuring secure, reliable file transfer for clinical data exchange with CROs, labs, and regulatory partners. Provide operational and functional support for eClinical Elluminate, including data review workflows, listings/reports configuration, and integration touchpoints with upstream/downstream clinical systems. Support EAST (Trial design and simulation platform) configuration, access provisioning, and issue triage. Lead incident, problem, and change management across all supported platforms — triaging tickets, performing root-cause analysis, and driving permanent fixes within SLA. Manage installation qualification (IQ), operational qualification (OQ), and performance qualification (PQ) activities, and maintain validation documentation (URS, FRS, test scripts, traceability matrices) for all platform changes. Coordinate patching, upgrades, DR/backup testing, and environment refreshes (Prod/UAT/Dev) in line with change control procedures. Ensure ongoing compliance with GxP, Part 11, data integrity (ALCOA+), and audit-readiness across all systems; support internal/external audits and regulatory inspections. Manage access control, user provisioning/de-provisioning, and periodic access reviews per SOX/GxP requirements. Develop and maintain SOPs, runbooks, knowledge base articles, and platform architecture documentation. Monitor capacity, licensing, and vendor SLAs; escalate and manage vendor relationships (SAS, Axway, Elluminate, Eclipse vendors) as needed. Conduct root cause analysis (RCA) for recurring incidents and implement corrective and preventive actions in coordination with Quality and IT teams. Support validation activities including IQ/OQ/PQ execution, traceability matrix development, and preparation of GxP-compliant documentation. Participate in go-live readiness activities, cutover planning, hypercare support, and post-implementation review. Lead teams comprising consultants and analysts and drive delivery within the quality and compliance workstream. Maintain comprehensive documentation including runbooks, SOPs, functional specifications, validation artefacts, and change management records. The successful candidate would possess these skills: Ability to work independently and collaborate as part of a teamEffective written and verbal communication skillsMeticulous attention to detail and quality of work productAbility to build and sustain professional relationships Ability to lead projects or workstreamsAbility to manage and prioritize multiple tasks in a fast-paced and dynamic environmentStrong interpersonal skills and professional demeanor Ability to meet deadlinesAbility to provide clear guidance to others The Team You will be part of the Clinical Data Analytics (CDA) Technology & Operations organization, which enables biostatistics, clinical data management, and real-world evidence functions with reliable, compliant, and scalable technology platforms. The team operates at the intersection of IT infrastructure, clinical operations, and quality/regulatory compliance, partnering closely with global business and technology stakeholders to support end-to-end clinical trial data lifecycles from data capture and coding through statistical analysis and submission-ready outputs. The team follows a managed-services model with defined SLAs, on-call rotation for critical platform support, and a strong culture of continuous improvement and regulatory rigor. Our Industry Solutions offering provides verticalized solutions that transform how clients sell products, deliver services, generate growth, and execute mission-critical operations. We deliver integrated business expertise with scalable, repeatable technology solutions specifically engineered for each sector. QualificationsRequired 6+ years of IT application support/administration experience in a pharmaceutical, biotech, or CRO environment, with 3+ years hands-on SAS Grid Administration.Experience supporting clinical/regulatory platforms in a GxP/validated environment, including change control, CSV (Computer System Validation), and audit support.Hands-on experience with Axway Secure Transport (ST) or equivalent secure managed file transfer (MFT) tools.Experience with Linux and Windows server administration in support of grid/application environmentsFamiliarity with GxP quality management concepts including 21 CFR Part 11, Annex 11, computerised system validation (CSV), and IQ/OQ/PQ documentation standards.Experience with Incident Management, Problem Management, and Change Management following ITSM/ITIL frameworks.Proficiency with ServiceNow and JIRA for ticket management, SLA tracking, and Agile project delivery.S/B.E / B.Tech / M.C.A. / M.Sc (CS) degree or equivalent experienceLimited immigration sponsorship may be available Ability to travel 10%, on average, based on the work you do and the clients and industries/sectors you serveRole is remote Preferred Experience with CDISC standards (SDTM/ADaM) as they relate to downstream SAS programming environments.SAS Certified Platform Administrator or SAS Certified Deployment Specialist credential.Familiarity with supplier qualification management and third-party audit management modules within QMS platforms.ServiceNow or equivalent ITSM tool experience for ticketing and change management.Experience supporting regulatory submissions (FDA/EMA) from a systems/platform readiness perspective. The wage range for this role takes into account the wide range of factors that are considered in making compensation decisions including but not limited to skill sets; experience and training; licensure and certifications; and other business and organizational needs. The disclosed range estimate has not been adjusted for the applicable geographic differential associated with the location at which the position may be filled. At Deloitte, it is not typical for an individual to be hired at or near the top of the range for their role and compensation decisions are dependent on the facts and circumstances of each case. A reasonable estimate of the current range is $120,200 - $140,000. You may also be eligible to participate in a discretionary annual incentive program, subject to the rules governing the program, whereby an award, if any, depends on various factors, including, without limitation, individual and organizational performance. Deloitte is committed to providing reasonable accommodations for people with disabilities. If you require a reasonable accommodation to participate in the recruiting process, please direct your inquiries to the Global Call Center (GCC) at View email address on click.appcast.io. Recruiting tips From developing a stand out resume to putting your best foot forward in the interview, we want you to feel prepared and confident as you explore opportunities at Deloitte. Check out recruiting tips from Deloitte recruiters. BenefitsAt Deloitte, we know that great people make a great organization. We value our people and offer employees a broad range of benefits. Learn more about what working at Deloitte can mean for you. Our people and culture Our inclusive culture empowers our people to be who they are, contribute their unique perspectives, and make a difference individually and collectively. It enables us to leverage different ways of thinking, ideas, and perspectives, and bring more creativity and innovation to help solve our clients' most complex challenges. This makes Deloitte one of the most rewarding places to work. Our purpose Deloitte’s purpose is to make an impact that matters for our people, clients, and communities. At Deloitte, purpose is synonymous with how we work every day. It defines who we are. Our purpose comes through in our work with clients that enables impact and value in their organizations, as well as through our own investments, commitments, and actions across areas that help drive positive outcomes for our communities. Learn more. Professional development From entry-level employees to senior leaders, we believe there’s always room to learn. We offer opportunities to build new skills, take on leadership opportunities and connect and grow through mentorship. From on-the-job learning experiences to formal development programs, our professionals have a variety of opportunities to continue to grow throughout their career. As used in this posting, "Deloitte" means Deloitte Consulting LLP, a subsidiary of Deloitte LLP. Please see for a detailed description of the legal structure of Deloitte LLP and its subsidiaries. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, disability or protected veteran status, or any other legally protected basis, in accordance with applicable law. Qualified applicants with criminal histories, including arrest or conviction records, will be considered for employment in accordance with the requirements of applicable state and local laws, including the Los Angeles County Fair Chance Ordinance for Employers, City of Los Angeles’s Fair Chance Initiative for Hiring Ordinance, San Francisco Fair Chance Ordinance, and the California Fair Chance Act. See notices of various fair chance hiring and ban-the-box laws where available. Fair Chance Hiring and Ban-the-Box Notices | Deloitte US Careers Requisition code: 364229 Job ID 364229 Package and Technology Enablement | Package Managed ServicesSame job available in 79 locations
$120k - $143k
...experienced Epic Willow Inpatient Senior Consultant you will have the ability to share new ideas... ...sector solutions in software, data, AI, network, and hybrid cloud infrastructure... ...equivalent experiencePreferredHospital or Clinic operations experienceAdditional Epic CertificationsITIL...DataSeniorLocal areaRemote work- ...REMOTE, USA The NAVLIN US Consulting Engagement Manager will play a... ...strategic thinking backed by robust data-driven tools to pure market... ...(researching topics such as clinical guidelines) and primary research... ...results. Take Action - I am empowered and hold myself...DataSeniorWork at officeLocal areaImmediate startRemote workShift work
$110.7k - $218.3k
Position Summary Senior Consultant - Digital Quality & ComplianceOur Deloitte Regulatory... .... Join our team and use advanced data, AI, and emerging technologies with industry... ..., biotechnology, medical device, or clinical environmentsExperience leading validation...DataSeniorVisa sponsorship$150k - $200k
...Weare seeking a high-quality Senior Manager/Associate Director of Clinical Pharmacology to lead the development and execution of clinical... ...Regulatory, Biometrics, etc.), and manage clinical pharmacology studies, data analysis, and regulatory filings. Essential Duties and...DataSenior$90k - $140k
...SystImmune SystImmune is a leading and well-funded clinical‑stage biopharmaceutical company located in... ...and IND‑enabling stages. The Scientist/Sr. Scientist, Clinical Pharmacology will... ...strategy to optimize study design, data interpretation, and regulatory submissions...DataSeniorFull time$72k - $141k
...potential. Leads smaller scale projects that involves the design, analysis and modeling of moderately complex to complex organizational data for a business area. Supports the active management of a business area by interpreting data and providing business insights.JOB...DataSeniorFull timeWork experience placementWork at officeRemote work$200k - $300k
SystImmune is a leading and well-funded clinical-stage biopharmaceutical company located in Redmond... ...this role could range across Director/Sr. Director/Exec Director based on the... ...temperament, and attention to details to drive data-informed decision making in a fast-paced...DataSeniorFull time- Integra LifeSciences in Princeton, NJ, is seeking an experienced leader to oversee end-to-end clinical data management across studies. You will guide study planning, data review, and regulatory compliance, while mentoring staff and coordinating with cross-functional teams...DataSenior
$131.04k - $196.56k
...feel like a fit? Then we would love to have you join us!The RoleThe Senior Manager, Clinical Programming is responsible for the establishment, governance, and integrity of Study Data Tabulation Model (SDTM) standards, perform sponsor oversight of relevant programming...DataSeniorFull timeFixed term contract$93k - $171.3k
Position Summary Senior Consultant, US Global StrategyThe US Global Strategy team is part of our Clients, Strategy, & Growth (CS&... ...enable businesses to lead and grow in dynamic markets, leveraging data-driven insights and deep industry specialization to anticipate...DataSenior$118k - $130k
...collaborative environment? As an experienced Regulatory Reporting Senior Consultant, you will have the ability to share new ideas and collaborate... ....Support regulatory exams, internal audits, and ad hoc data requests related to fund regulatory reporting.Drive continuous...DataSeniorLocal areaVisa sponsorship$110.7k - $218.3k
Position Summary Google Gemini, Senior Consultant, Technical Transformation Our Deloitte Sales & Service team empowers organizations... ..., commerce, sales, and service. We are a team of strategists, data scientists, operators, creatives, designers, engineers, and...DataSeniorLocal area$95k - $155k
...business processes, modernize their technology landscape, improve data quality, streamline integrations, and increase operational efficiency through the SAP Reinsurance Management solution. Our consultants work on complex international projects, collaborate closely with...DataSeniorWorldwide$110.7k - $218.3k
Position Summary Senior Consultant - Capital Markets Operations and Technology Our Enterprise Operations & Risk practice empowers... ...innovative and emergent technologies, including cloud computing, big data and analytics, process automation, artificial intelligence /...DataSeniorWork at office- Job DescriptionSenior Consultant- Research and Development, Life SciencesWe’re seeking a Senior... ...Consultant who blends R&D domain depth (Clinical, Safety, Regulatory) with consulting... ...business needs into scalable processes, data, and platform solutions, enabling efficiencies...DataSeniorFull timeTemporary workLocal area
$105.4k - $207.8k
...whom they are dealing and ensuring the integrity of access to data.QualificationsRequired:Bachelor’s degree in Computer Science, Cyber... ...immigration sponsorship may be available.Preferred:Previous consulting or Big 4 experienceCyberArk/Beyond Trust/Delinea certifications...DataSeniorLocal areaVisa sponsorship$105k - $207k
...Recruiting for this role ends on 10/02/2026. Work you'll do As a Senior Consultant, Technical Transformation on the Business Finance team, you... ...integration of OneStream with enterprise platforms, data sources, and downstream systems to support solution performance...DataSeniorLocal area$110.7k - $218.3k
...of experience integrating Appian applications with enterprise data sources, application programming interfaces, and third-party services... .... As used in this posting, "Deloitte" means Deloitte Consulting LLP, a subsidiary of Deloitte LLP. Please see for a detailed...DataSeniorLocal areaFlexible hours$65 - $80 per hour
...for patients. Title: Senior Manager/Associate Director, Clinical Quality Location: Princeton, NJ Schedule: Hybrid... ...protocol deviations, risk assessments, participant safety, and data integrity. Partner with Clinical Development, Clinical...DataSeniorPermanent employmentContract work2 days per week$105k - $207k
...stakeholders into tailored OneStream applicationsBuild and support data integration and automation capabilities that enable effective... .... As used in this posting, "Deloitte" means Deloitte Consulting LLP, a subsidiary of Deloitte LLP. Please see for a detailed description...DataSeniorLocal area$130.72k - $196.08k
...based therapeutics to improve the lives of patients. As a Senior Clinical Trial Manager (CTM), you will play a pivotal role in driving the... ...of trial-level challenges.Monitor trial performance and data quality, leveraging key metrics to drive decision-making and continuous...DataSeniorFull timeFixed term contract- ...protocol compliance and deviationsCRF review and data correctionsIMP accountabilityMaintenance... ...and potential site and study issuesEnsure clinical data integrity and adherence to study... ...oncology Phase I-III studies required for Sr CRA considerationSkills and CompetenciesKnowledge...DataSeniorFull timeWork experience placementRemote workRelocationFlexible hoursNight shift
- Job DescriptionSenior Consultant - Project Manager, Life Sciences, Infosys Consulting The Role... ...pharmaceutical firms to modernize clinical trial operations and improve patient engagement... ...market access. Managing enterprise-wide data governance programs to ensure data...DataSeniorFull timeTemporary workLocal area
- ...Early Development, the Senior Director, Clinical Pharmacology will provide strategic and... ...activities currently supported by external consultants into an internally led capability.... ...interpretation of clinical pharmacology data. Oversee external clinical pharmacology...DataSenior
$235k - $255k
...facility for an experienced R&D/Clinical Quality leader to oversee our... ...) to support patient safety, data integrity, product quality and... ...for CROs, CMOs, laboratories, consultants and development partners.Lead... ...Clinical Development). REQUIREDFor SR or EX Director:Significant...DataSeniorFull timeContract workWork at officeLocal area$230k - $300k
...Description Job Description SystImmune is a leading and well-funded clinical-stage biopharmaceutical company located in Redmond, WA and... ...collaborate across functions to deliver high-quality clinical data that supports product development, regulatory submissions, and business...DataSenior$180k - $220k
...a difference. About the Role We’re seeking a Senior Director, Clinical Operations to lead Clinical Project Managers and Clinical Research... ...improvement initiatives based on audit and inspection findings, data, KPIs and metrics. Participates in related professional...DataSeniorWork at officeRelocationFlexible hours$90k - $140k
...Senior Clinical Research Associate SystImmune is a leading and well-funded clinical-stage... ...support SystImmune's clinical trials. The Sr. CRA is responsible for the management and... ...their assigned clinical study sites to ensure data quality and patient safety in accordance...DataSeniorContract workInterim roleWork at officeLocal areaRemote work$157.25k - $185k
...patients. Advanced technology, a world-class clinical development organization, and state-of-... ..., drug disposition, and drug metabolism data from clinical studies for TOI oncology... ...ability to effectively manage external consultants and third-party CROs. Strong...DataSeniorLocal area$20 - $23 per hour
...to, patients, caregivers, healthcare providers, and healthcare clinic personnel. This role will work on a hybrid schedule, 2 days in our... ...related to pharmaceutical contact center operations, including data privacy and security requirements Essential Requirements: High school...DataHourly payWork at officeLocal areaRemote workFlexible hours
Do you want to receive more vacancies?
Subscribe and receive similar vacancies to Clinical Data AMS Sr. Consultant. Be the first to apply!


