Referso Jobs

Senior Manager, Clinical Data

Precigen, Inc · Posted Nov 10, 2026

Open

Germantown, Maryland, United States
Senior
7+ years

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Senior Manager, Clinical Data

Precigen, Inc · Posted Nov 10, 2026

Open

Germantown, Maryland, United States
Senior
7+ years

Apply with Referso

Manager, Drug Safety Operations

Precigen, Inc · Posted Nov 10, 2026

Open

Germantown, Maryland, United States
Manager
3–5 years

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Lead day‑to‑day pharmacovigilance operations, managing vendor relationships, ensuring regulatory compliance, and supporting safety reporting.

Responsibilities

Manage day‑to‑day relationships with PV vendors
Coordinate vendor selection activities
Support negotiation and maintenance of contracts, SOWs, change orders, and PVAs/SDEAs
Track and report KPIs and SLAs
Monitor vendor adherence to US and international PV regulations

Requirements

Bachelor’s degree in life sciences, nursing, pharmacy, or a related field

Skills

pharmacovigilance vendor oversight safety databases Argus ICSR processing PV regulations GVP 21 CFR 312/314 ICH E2 series

Lead DM (FSP)

Parexel · Posted Nov 6, 2026

Open

Shanghai, China

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Lead Data Management (FSP) responsible for data validation, database lock, user acceptance testing, and operational support in clinical trials.

Responsibilities

Lead and coordinate data validation activities during conduct and database lock
Manage query resolution and vendor data reconciliation
Support setup of data management documents and SOP compliance
Lead user acceptance testing on clinical database setups
Review protocols and EDC entry screens

Requirements

Bachelor’s degree or equivalent medical qualification

Skills

Data validation Data cleaning Database lock SAS CDISC MedDRA WHODrug Clinical Data Management Systems InForm Rave Veeva Data Labs ClinBase

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Clinical Data Management Lead (Contract)

Kriya Therapeutics · Posted Nov 5, 2026

Open

Remote
Remote
Contract
8+ years

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Lead clinical data management activities across Kriya Therapeutics' clinical development programs, ensuring data quality, integrity, and regulatory compliance.

Responsibilities

Execute day‑to‑day clinical data management activities for assigned studies
Develop and maintain study‑specific data management plans, CRF guidelines, and data validation specifications
Lead CRO data management activities and ensure deliverables meet quality standards
Serve as data management contact for cross‑functional study teams
Ensure compliance with FDA, ICH‑GCP, and other regulatory requirements

Requirements

Bachelor's degree in life sciences, health informatics, or computer science
Advanced degree preferred

Skills

clinical data management database design edit checks CRF design MedDRA WHODrug CDISC

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