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Overnight Oracle Argus Safety Jobs (NOW HIRING)

Collabera

Safety Systems Analyst

Jersey City, NJ

Oracle AERS, ARISg, ARGUS) and excellent technical, analytical and problem solving skills pertaining to safety database systems. Individual should have excellent communication skills and ...

Apex IT

Oracle Cloud HCM Solution Architect

$64.50 - $85/hr

... the travel is overnight, varies. Job Summary: The Oracle Cloud HCM Architect owns the client ... Health & Safety § Oracle Cloud Talent Management • Workforce Compensation • Learning • ...

Oracle

System Administrator 1-IT

Kansas City, MO · On-site

$25.82 - $50.43/hr

Please be advised, this position is a standardized overnight/off-hours shift. Conducts end-to-end ... Safety and Compliance-Safety, Security, Compliance, and Documentation:-Learns and follows all ...

Ryan Companies

Capital Markets Associate

Minneapolis, MN · On-site +1

$120K - $150K/yr

Occasional overnight travel expected. To be successf ul in this role, you must have: * Bachelor ... Strong working knowledge of Argus is a plus You will really stand out if you have: * Proficient in ...

Ryan Companies

Capital Markets Associate

Chicago, IL · On-site +1

$120K - $150K/yr

Occasional overnight travel expected. To be successf ul in this role, you must have: * Bachelor ... Strong working knowledge of Argus is a plus You will really stand out if you have: * Proficient in ...

Ryan Companies

Capital Markets Associate

Chicago, IL · On-site

$120K - $150K/yr

Occasional overnight travel expected. To be successf ul in this role, you must have: * Bachelor ... Strong working knowledge of Argus is a plus You will really stand out if you have: * Proficient in ...

Portman

Development Manager

Atlanta, GA · On-site

Participates in Company-provided training such as safety, non-discrimination, information systems ... ARGUS, MS Office, and Microsoft Project Software * Business Travel as needed with overnight stay ...

TGG Accounting

Project Manager

Middlesex, VT · On-site

Lead project meetings to review schedules, budgets, safety, production goals, and overall project ... Maintain accurate project documentation using Procore, Primavera P6 (Oracle), and other project ...

TGG Accounting

Project Manager

Montpelier, VT · On-site

Lead project meetings to review schedules, budgets, safety, production goals, and overall project ... Maintain accurate project documentation using Procore, Primavera P6 (Oracle), and other project ...

TGG Accounting

Project Manager

Middlesex, VT

Lead project meetings to review schedules, budgets, safety, production goals, and overall project ... Maintain accurate project documentation using Procore, Primavera P6 (Oracle), and other project ...

TGG Accounting

Project Manager

Middlesex, VT · On-site

Lead project meetings to review schedules, budgets, safety, production goals, and overall project ... Maintain accurate project documentation using Procore, Primavera P6 (Oracle), and other project ...

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Overnight Oracle Argus Safety information

What is the difference between Overnight Oracle Argus Safety vs Clinical Data Coordinator?

AspectOvernight Oracle Argus SafetyClinical Data Coordinator
CertificationsOracle Argus Safety certification, pharmacovigilance trainingClinical research certifications, GCP training
Work EnvironmentPharmaceutical companies, CROs, pharmacovigilance teamsClinical trial sites, research organizations
Industry UsagePharmacovigilance, drug safety monitoringData management, trial coordination

Overnight Oracle Argus Safety professionals focus on drug safety and pharmacovigilance using Oracle Argus Safety software, often working in pharmacovigilance teams. Clinical Data Coordinators handle clinical trial data collection and management, primarily at research sites. While both roles require attention to detail and industry-specific certifications, they serve different functions within the clinical research and drug safety landscape.

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Overnight Oracle Argus Safety jobs near you
Infographic showing various Overnight Oracle Argus Safety job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 79% Full Time, 17% Part Time, 2% Contract, and 1% Nights. Highlights an 99% Physical, and 1% Remote job distribution.

Manager, Pharmacovigilance Operations

Allogene Therapeutics

South San Francisco, CA • On-site, Remote

$140K - $150K/yr

Full-time

Medical

Posted 16 days ago

Job description

Job Description
About Allogene:
Allogene Therapeutics, with headquarters in South San Francisco, is a clinical-stage biotechnology company pioneering the development of allogeneic chimeric antigen receptor T cell (AlloCAR T) products for cancer and autoimmune disease. Led by a management team with significant experience in cell therapy, Allogene is developing a pipeline of "off-the-shelf" CAR T cell product candidates with the goal of delivering readily available cell therapy on-demand, more reliably, and at greater scale to more patients.
About the role:
We are seeking a highly motivated Manager, Pharmacovigilance Operations to join our team. You will provide support to the Allogene Pharmacovigilance department for drug safety operations including safety vendor oversight and management, serious adverse event reporting, support of study teams and projects, oversight of global safety database activities, and collaboration to support risk management and pharmacovigilance for all Allogene Therapeutics Clinical Trials and post marketing (where applicable). You will be interfacing cross-functionally at many levels in the organization as well as with our external vendors. You will be self-motivated, have strong communication and teamwork skills along with a robust ability to work independently, problem solve, manage work priorities, build collaborative relationships, and remain flexible to the needs of the teams and projects. This position will report to the Director, Pharmacovigilance. This role can be remote with frequent to travel to Allogene's South San Francisco headquarters or can be based out of our headquarters in South San Francisco, CA hybrid onsite 3 days a week.
Responsibilities include, but are not limited to:
  • Assist in Safety Vendor Oversight activities including tracking of KPIs, compliance metrics, and open query metrics.
  • Participate in eTMF filing for Allogene studies per TMF plans and procedures.
  • Schedule meetings and manage meeting agenda for PV team. Support Study Management Team meetings as needed.
  • Facilitate the preparation, completion, and submission of periodic safety reports (DSUR, 6M LL, etc.) and other regulatory filing documents.
  • Assist in MedDRA and WHODrug coding as needed.
  • Collaborate with the preparation and updates to safety section in the Investigator Brochures, RSI, DSURs, Protocols, ICFs, etc.
  • Manage Regulatory Reporting Requirements across all studies, ensure all requirements are met by the most current regulations.
  • Support projects or other initiatives from cross functional groups and departments
  • Support SPEED access requests and maintain the tracker, resolve access issues as applicable, perform monthly reconciliation.
  • Support SAE reconciliation between Clinical and Safety databases as needed.
  • Manage safety mailbox and provide responses to relevant communications.
  • Maintain internal and external distributions lists including providing updates and communications as appropriate.
  • Assist in the development and approval of PV SOPs and Work instructions
  • Initiate SMP review per schedule
  • Liaise with QA for CAPA activities in relation to, but not limited to, late SUSAR or aggregate report submissions as well as deviations relating to case management processes as defined per the SMPs or SOPs
  • Maintain SUSAR tracker in real time, perform monthly reconciliation and identify/resolve issues in timely manner.
  • Participate in regulatory inspections and PV audits to ensure quality, integrity and compliance with pharmacovigilance and safety reporting requirements
  • Other duties and projects as assigned

Position Requirements & Experience:
  • Bachelor's degree in life sciences, healthcare, or a related discipline; advanced degree (e.g., RN, BSN, PharmD) preferred
  • Minimum of 5 years of pharmacovigilance experience in a pharmaceutical or biotechnology company
  • Solid understanding and working knowledge of US and ex-US pharmacovigilance regulatory requirements (e.g., US Code of Federal regulations; European Union GVP legislation; and ICH Guidelines)
  • Proficiency in safety databases and other systems (e.g., Oracle Argus, ARISg, MedDRA, WHODrug, SPEED)
  • Excellent organizational skills and an ability to prioritize effectively to deliver results within reasonably established timelines
  • Ability to work independently and collaboratively in a fast-paced environment and manage multiple projects simultaneously.
  • Experience with device safety reporting, eTMF filing, and regulatory inspections is a plus.
  • Strong interpersonal skills including verbal and written communication are essential in this collaborative work environment
  • Candidates must be authorized to work in the U.S.

We offer a chance to work with talented people in a collaborative environment and provide a top-notch compensation and benefits package, which includes an annual performance bonus, equity, health insurance, generous time off (including 2 annual holiday company-wide shutdowns) and much more. The expected salary range for this role is $140,000 to $150,000 per year. Actual pay will be determined based on experience, qualifications, geographic location, business needs, and other job-related factors permitted by law.
As an equal opportunity employer, Allogene is committed to a diverse workforce. Employment decisions regarding recruitment and selection will be made without discrimination based on race, color, religion, national origin, gender, age, sexual orientation, physical or mental disability, genetic information or characteristic, gender identity and expression, veteran status, or other non-job-related characteristics or other prohibited grounds specified in applicable federal, state and local laws. We also embrace differences in experience and background, and welcome diversity of opinions and thought, designed to create a stronger and better Allogene that is focused on developing life-changing products for patients.

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