Source Job

14 jobs similar to Principal Database Programmer (LATAM)

Jobs ranked by similarity.

$180,000–$210,000/yr
US

  • Function as lead programmer to produce and/or validate tables, listings, figures, and analysis datasets.
  • Develop/review TFL shells, SDTM and ADaM specifications in collaboration with biostatisticians and other clinical development colleagues.
  • Work closely with Data Management and Biostatistics to ensure final databases, analyses, and reports are accurate.

Nuvalent is working to create selective medicines designed with the goal to address the needs of patients with cancer using its expertise in chemistry. Nuvalent is an early-stage company bringing together experienced scientists and industry veterans with a proven track record in oncology drug development.

$155,000–$190,000/yr
US

  • Lead statistical programming efforts for clinical studies.
  • Oversee and coordinate activities with Contract Research Organizations (CROs).
  • Collaborate closely with statisticians and cross-functional study teams to deliver results in a timely and accurate manner.

Kailera is developing therapies that give people the power to transform their lives and elevate their overall health. Rooted in an entrepreneurial spirit and a team-oriented culture, they are working together to advance novel therapies for obesity and related conditions.

US

  • Support the design, specifications, and development of eCRFs
  • Develop Data Management Plan documents
  • Manage effective communication of data issues and discrepancies to study sites via the query management process

Kyverna Therapeutics is a patient-centered, clinical-stage biopharmaceutical company developing cell therapies for patients suffering from autoimmune diseases. They are committed to transforming the future of treatment for autoimmune disease and redefining what’s possible.

$175,000–$192,000/yr
US

  • Responsible for timelines and quality of CDM deliverables for the assigned studies.
  • Manages CDM timelines to coordinate and synchronize deliverables with the overall study timelines.
  • Responsible for the accuracy and completeness of the clinical data collected during a clinical trial.

Celcuity is a clinical-stage, publicly traded biotechnology company seeking to extend the lives of cancer patients through the development of targeted therapies. They are committed to fair and equitable compensation practices and strive to provide employees with competitive total compensation packages.

US

  • Develop and implement software applications using a variety of languages, frameworks, and methodologies.
  • Establish host environments for software applications with community-based health care settings.
  • Perform data extracts against databases and other data sources, to analyze extracted data and to summarize results.

The Division of Informatics, Clinical Epidemiology and Translational Data Science (DICE) is an academic unit within OHSU’s Department of Medicine that focuses on improving healthcare practice and outcomes through informatics tools and data analytics. DICE engages in research related to the development, dissemination, and evaluation of information technology and outcomes research in the healthcare field.

Europe

  • Program Lead IT Operations at our customers for Veeva’s R&D SaaS solutions
  • Function as a Primary customer liaison managing communication between managed services teams, customer stakeholders, and 3rd parties
  • Oversee customer release management programs including resource planning, release tracking, and forecasting

Veeva Systems is a mission-driven organization and pioneer in industry cloud, helping life sciences companies bring therapies to patients faster. As one of the fastest-growing SaaS companies in history, they surpassed $2B in revenue in their last fiscal year with extensive growth potential ahead.

US

  • Provides validation and UAT support for Clinical Data Management activities across studies.
  • Leads and coordinates functions for multiple assigned projects related to the planning, execution, collection, and cleaning of clinical data.
  • Works within the company’s SOPs, guidelines and standards to ensure data integrity at all times.

Iovance Biotherapeutics is committed to cultivating and offering a diverse and inclusive work environment. As an equal-opportunity employer, their employees and applicants will be considered without regard to an individual’s race, color, religion, sex, pregnancy, national origin, age, physical and mental disability, marital status, sexual orientation, gender identity, gender expression, genetic information, military and veteran status, and any other characteristic protected by applicable law.

US

  • Working collaboratively with stakeholders, address hypotheses across various disease and treatment areas, leveraging the Atropos platform.
  • Run custom analytics using Atropos Health's proprietary technology stack + industry standard tools and analysis packages.
  • Own end-to-end hypothesis generation and study generation across multiple health care domains

Atropos Health develops GENEVA™ OS, an operating system for rapid healthcare evidence using real-world data. They aim to transform healthcare with timely, relevant real-world evidence, fostering a diverse, inclusive, and equitable workplace.

$204,000–$245,000/yr

  • Lead statistical support for early- and late-phase clinical studies.
  • Lead the development, execution, and interpretation of statistical analyses.
  • Lead the development and the adoption of innovative statistical approaches.

Kailera develops therapies that give people the power to transform their lives and elevate their overall health. They are rooted in an entrepreneurial spirit and a team-oriented culture, working together to advance novel therapies for obesity and related conditions.

$138,237–$138,237/yr
US

  • Collaborate with implementation teams and external customers to ensure data integrity and interface validation for symplr software solutions.
  • Analyze and manage patient healthcare data for consistency and accuracy while configuring system software during implementation projects.
  • Leverage analytical, technical, and communication skills to define processes for clinical data management and assist customers in achieving their organizational goals.

Symplr is revolutionizing healthcare operations with a first-of-its-kind platform that drives effective, efficient, and connected workflows, increasing operational benefits and scaling clinical, financial, and quality outcomes. We are a remote-first company with employees across the United States, India, and the Netherlands.

Europe

  • Data preparation and cleaning of raw clinical trial data for PK/PD analysis.
  • Writing R or Rmarkdown code for descriptive and statistical analysis of PK/PD data.
  • Ensuring CDISC compliance for regulatory submissions.

Jobgether uses an AI-powered matching process to ensure applications are reviewed quickly, objectively, and fairly. They identify top-fitting candidates and share the shortlist with the hiring company.

Mexico

  • Support the primary TAM in monitoring the health and performance of Varicent solutions across a portfolio of VIP customers.
  • Assist in coaching users on foundational Varicent functionality, configuration concepts, and best-practice methodologies.
  • Contribute to configuring Varicent solutions based on documented customer requirements, under guidance from the senior TAM.

Varicent is a company that transforms the Sales Performance Management (SPM) market and redefines how organizations achieve revenue success. Their SaaS solutions empower revenue leaders globally to design smarter go-to-market strategies and maximize seller performance.

LATAM

  • Oversees and supports country level feasibility, Investigator identification and selection, if applicable.
  • Responsible for overall management of project allocated direct reports (CRAs, Site Managers and CTAs, as applicable).
  • Coordinates and ensures the adequate preparations for site specific audits and inspections.

Ergomed is a rapidly expanding full-service mid-sized CRO specializing in Oncology and Rare Disease. They have operations in Europe, North America and Asia and values employee experience, well-being and mental health.

  • Accountable for study level tracking as assigned by the Clinical Project Manager.
  • Ensures patient enrollment activities are conducted in a timely manner and is comfortable communicating with site personnel.
  • Acts as QC of Trial Master Files; creates, maintains, and closes out TMFs; is key in set up, conduct, and close out of ancillary services.

Akero Therapeutics, a Novo Nordisk company, is focused on discovering and developing transformational treatments for patients with serious metabolic diseases. They are a team of problem solvers dedicated to pursuing bold scientific approaches to build a brighter future for patients.