Referso Jobs

Associate Director, Patient Safety Scientist

AstraZeneca · Posted Nov 9, 2026

Open

Gaithersburg, Maryland, United States
Hybrid
Full-time · Manager
$132K–$199K per year

Associate Director, Patient Safety Scientist

AstraZeneca · Posted Nov 9, 2026

Open

Gaithersburg, Maryland, United States
Hybrid
Full-time · Manager
$132K–$199K per year

Associate Director, Patient Safety Scientist

AstraZeneca · Posted Nov 9, 2026

Open

Gaithersburg, Maryland, United States
Hybrid
Full-time · Manager
$132K–$199K per year

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Lead safety science activities for cell therapy assets within the Global Patient Safety Unit, integrating data, managing risks, and supporting regulatory submissions.

Compensation

The annual base pay for this position ranges from $132K to $199K. Our positions offer eligibility for multiple incentives an opportunity to receive short-term incentive bonuses, equity-based awards for salaried roles and commissions for sales roles.

Responsibilities

Conduct and coordinate safety surveillance, signal detection, validation, evaluation and management for assigned cell therapy assets
Develop MedDRA search strategies
Translate safety data into analyses and recommendations
Lead pharmacovigilance and risk‑management planning
Author and project‑manage safety reports and deliverables

Requirements

Bachelor’s degree in life sciences, pharmacy, nursing or a related discipline
Advanced degree in immunology, autoimmune disease, pharmacology or a related discipline
Nice to have: MSc
Nice to have: PhD
Nice to have: PharmD

Skills

safety science pharmacovigilance signal management periodic safety reports

Director, DSPV Data, Technology and Innovation

Insmed Incorporated · Posted Oct 29, 2026

Open

Remote
Remote
Full-time · Manager
$185K–$253K per year
10+ years

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Business owner of Insmed's safety systems, accountable for DSPV data, technology and innovation strategy and roadmap.

Compensation

$185,000.00-252,500.00 Annual

Responsibilities

Define and approve business requirements, configuration decisions, user access, and release priorities for safety systems
Own the business relationship with safety systems and technology vendors
Act as main point of contact between DSPV and Insmed IT
Hold vendors and contractors accountable for quality and timeliness
Monitor capacity, performance and stability of safety systems

Requirements

Bachelor's degree in a scientific, computational, health-related or information systems discipline
Advanced degree in a related field preferred
Nice to have: AI, machine learning, natural language processing
Nice to have: Real-world evidence applications
Nice to have: Python

Skills

Business ownership of safety database Safety system implementation Safety data migration Project management of technology projects

Project Manager, Patient Safety

Lifelancer · Posted Nov 9, 2026

Open

Remote, Canada
Remote
Full-time
CA$105K–CA$123K per year
2+ years

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Lead global drug safety projects, manage a portfolio of safety projects, and serve as the trusted safety partner for sponsors.

Compensation

Pay Range: CAD 105,000-123,000

Responsibilities

Lead and manage global or regional safety projects
Oversee adverse event processing
Oversee expedited safety reports
Perform or oversee quality review, signal detection, trend recognition and aggregate reporting
Prepare Safety Management Plans, reconciliation plans and monthly status reports

Requirements

Non-degree plus 6–7 years' safety experience
Associate degree (including RN) plus 5–6 years' safety experience
BS/BA plus 4–5 years' safety experience
MS/MA plus 2–3 years' safety experience
PharmD plus 1–2 years' safety experience

Skills

project management safety leadership pharmacovigilance client and sponsor-facing skills negotiation

Medical Coder - Operations

Careers Signant Health · Posted Nov 6, 2026

Open

Noida, Uttar Pradesh, India

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Responsible for medical coding services for clinical trials, ensuring accurate and timely deliverables.

Responsibilities

Codes medical terms, adverse events, and concomitant medications using MedDRA and WHODrug across multiple clinical trials.
Leads resolution of complex coding issues and discrepancies.
Performs encoder user acceptance testing.
Authors relevant sections of the data management plan (DMP).
Ensures compliance with regulatory requirements for clinical trial coding (e.g., FDA, EMA).

Requirements

Bachelor’s degree in a relevant medical field or equivalent work experience
Nice to have: 2+ years of professional experience in medical coding in the clinical trials data space
Nice to have: Familiarity with 21 CFR Part 11 or experience in a regulated environment

Skills

MedDRA coding WHODrug coding Access Excel office software technologies

See full job description

Manager Medical Review

Regeneron · Posted Nov 5, 2026

Open

Hyderabad, Telangana, India
On-site
Manager
7–9 years

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Lead end‑to‑end medical review of Individual Case Safety Reports for global development programs and selected marketed products.

Responsibilities

Perform complete medical review of Individual Case Safety Reports within defined timelines
Review and strengthen case narratives, analyses of similar events, company causality rationales, and reporting decisions
Determine expectedness using current reference safety information
Apply MedDRA coding to adverse events and medical histories
Partner with pharmacovigilance teams, risk management leads, and clinical development leads to produce cohesive, submission‑ready case documentation

Requirements

MD or MBBS with active registration or eligibility for registration with the relevant Indian professional regulatory body
Nice to have: AI or generative AI tools in pharmacovigilance, safety review, or clinical documentation

Skills

MedDRA coding ICH E2A, E2B, E2D guidelines FDA and EMA pharmacovigilance requirements Oracle Argus Safety

Associate Director - Senior Case Manager

Eli Lilly and Company · Posted Nov 3, 2026

Open

Indianapolis, Indiana, United States
Full-time · Manager
$117K–$172K per year
5+ years

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Senior hands‑on practitioner for Individual Case Safety Report (ICSR) work across intake, processing and regulatory submission.

Compensation

$117,000 - $171,600

Responsibilities

Act as key operational decisionmaker on complex ICSR validity questions
Monitor operational metrics and trends to identify emerging risks
Resolve difficult, complex, duplicate and linked‑case scenarios
Provide audit and inspection support for case management operations
Coach case managers and vendor trainers on difficult case scenarios

Requirements

Bachelor’s degree
Nice to have: coaching case processors
Nice to have: calibrating case processors
Nice to have: knowledge of ICSR reporting requirements
Nice to have: automation tools

Skills

ICSR processing data entry submission quality checking safety database Argus safety database Veeva Vault

Associate Director, Patient Safety Scientist

Associate Director, Patient Safety Scientist

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Associate Director, Patient Safety Scientist

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Director, DSPV Data, Technology and Innovation

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Project Manager, Patient Safety

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Medical Coder - Operations

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Manager Medical Review

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Associate Director - Senior Case Manager

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MedDRA coding jobs

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