Data Engineer (Marketing-oriented) | Remote for Marketing Agency for Education
Our client is a fast-growing performance marketing agency specializing in mission-driven organizations across higher education and nonprofit sectors.
Since launching in ****, the agency has built a strong reputation for combining strategic thinking, creative execution, and data-driven marketing to help universities and organizations achieve measurable growth.
Your Role:
The Senior Data Engineer sits at the center of the agency's Data and Analytics function, connecting every paid media platform and CRM the agency touches into a single, reliable source of truth.
You'll own the full path data takes: from a client's ad accounts and CRM, through Adverity, into a BigQuery warehouse, through modular dbt/Dataform transformations, and out to the Looker Studio dashboards and automated Google Sheets reports the team and its partners rely on daily.
Reporting to the Data and Analytics Manager, you're joining at a pivotal moment — the agency is scaling its roster of education and nonprofit partners, and this role is instrumental in evolving the automated reporting suite that makes that growth possible without sacrificing data quality or client trust.
You'll:
Own data ingestion & pipeline architecture — connect and maintain API pipelines from paid media platforms (Meta, Google Ads, LinkedIn, TikTok, programmatic) into Adverity, build custom Python connectors for anything not natively supported, and architect scalable pipelines from source system through to dashboard
Own CRM integration — build and maintain rate.Demonstrates diligence in protecting the confidentiality of each subject/patient.Assesses factors that might affect subject/patient's safety and clinical data integrity at an investigator/physician site such as protocol deviation/violations and pharmacovigilance issues.Per the Clinical Monitoring/Site Management Plan (CMP/SMP):



Assesses site processes.Conducts Source Document Review of appropriate site source documents and medical records.Verifies required clinical data entered in the case report form (CRF) is accurate and complete via review of site source documents and medical records.Applies query resolution techniques remotely and on site, and provides guidance to site staff as necessary, driving query resolution to closure within agreed timelines.Utilizes available hardware and software to support the effective conduct of the clinical study data review and capture.Verifies site compliance with electronic data capture requirements.May perform investigational product (IP) inventory, reconciliation and reviews storage and security.Verifies the IP has been dispensed and administered to subjects/patients according to the protocol.Verifies issues or risks associated with blinded or randomized information related to IP.Applies knowledge of GCP/local regulations and organizational procedures to ensure IP is appropriately (re)labelled, imported and released/returned.Routinely reviews the Investigator Site File (ISF) for accuracy, timeliness and completeness.Reconciles contents of the ISF with the Trial Master File (TMF).
Ensures the investigator/physician site is aware of the requirement of archiving essential documents in accordance with local guidelines and regulations.Documents activities via confirmation letters, follow-up letters, trip reports, communication logs, and other required project documents as per SOPs and Clinical Monitoring Plan/Site Management Plan.Supports subject/patient recruitment, retention and awareness strategies.Enters data into tracking systems as required to track all observations, ongoing status and action items to resolution.Understands project scope, budgets,



and timelines for own and others' activities in the clinical team; manages site-level activities / communication to ensure project objectives, deliverables and timelines are met.Must be able to quickly adapt to changing priorities to achieve goals / targets.May act as primary liaison with study site personnel, or in collaboration with Central Monitoring Associate.Ensures all assigned sites and project-specific site team members are trained and compliant with applicable requirements.Prepares for and attends Investigator Meetings and/or sponsor face to face meetings.Participates in and may lead general clinical monitoring/project staff meetings (inclusive of Sponsor representation, as applicable) and attends clinical training sessions according to the project specific requirements.Provides guidance at the site and project level towards audit readiness standards and supports preparation for audit and required follow-up actions.May provide direct supervision, training and/or mentorship to more junior level CRAs.Performs training and sign off visits for junior CRA staff, as assigned.May be mentored and assigned lead tasks under supervision of an experienced Clinical Operations Lead (COL) or operational line manager.This could include participation in business development proposals and/or defense meetings.For Real World Late Phase (RWLP), the Sr.
CRA II will use the business card title of Sr.Site Management Associate II.Additional responsibilities include: Site support throughout the study lifecycle from site identification through close-out.Knowledge of local requirements for real world late phase study designs.Chart abstraction activities and data collection.As required, collaborate and build relationship with Sponsor and other affiliates, medical science liaisons and local country staff.The SMA II may be requested to train junior staff.Identify and communicate out of scope activities to Lead CRA/Project Manager.Proactively suggest poten-world data engineering case study)
Final Interview with company leadership
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📌 Senior Data Engineer — Remote Data Pipelines & Analytics (Santa Fe)
🏢 Atomic Hr
📍 Santa Fe