Associate Manager, Centralized Monitoring

Benefits

Parental leave

Not verified

Non-birth-parent leave

Not verified

Family-building benefits

• Fertility benefits: Not verified
• Adoption assistance: Not verified
• Surrogacy assistance: Not verified

Mental health support

Not verified

Relocation assistance

Not verified

Childcare support

Not verified

Learning budget

Not verified

Verification

Not verified checked Jun 13, 2026

Salary

$115K-$144K From the posting source checked Jun 20, 2026

401(k) match

Reported from DOL Form 5500 industry filing (not employer-specific)

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Market context

U.S. role benchmark (BLS OEWS)

$61,842 U.S. median for this role

Projected growth (BLS Employment Projections)

+1.9% - Slower

U.S. benchmark only; posted salary is not compared across countries or currencies.

Matched to SOC 11-1021 - Operations aggregate by role bucket.

Source: U.S. Bureau of Labor Statistics, OEWS, May 2024 and Employment Projections, 2024-2034.

Role

Role function

Operations From the posting source checked Jun 20, 2026

Seniority

Mid From the posting source checked Jun 20, 2026

Work mode

Remote From the posting source checked Jun 20, 2026

In-office days

0 days From the posting source checked Jun 20, 2026

Schedule

Shift type

Not verified

Weekend work

Not verified

Company

Company stage

Public-company From the posting source checked Jun 20, 2026

Equity

Offered Verified - SEC 10-K source checked Jun 20, 2026

Application

Cover letter

Not verified

Assessment

Not verified

Deadline

Not stated

Where they hire

State eligibility is not yet verified.

About this role

Associate Manager, Centralized Monitoring Remote Position Summary: The Associate Manager, Centralized Monitoring is responsible for executing and overseeing centralized monitoring activities across clinical trials using a risk-based quality management (RBQM) framework. The role focuses on proactive signal detection, data surveillance, risk identification support, and escalation to support study quality, participant safety, and regulatory compliance. This position also contributes to process improvement, and cross-functional collaboration related to centralized monitoring activities. Incumbent will support cross-functional collaboration across multiple clinical studies, with a focus on regulatory compliance and inspection readiness. Essential Job Functions and Responsibilities: These may include but are not limited to: Support the execution of centralized monitoring strategies for studies ensuring setup aligns with Crinetics' RBQM best practices. Perform ongoing centralized monitoring reviews using clinical, operational, and quality data sources (e.g., EDC, CTMS, safety, vendor data). Identify emerging study-level and site-level risks through Key Risk Indicators (KRIs), Quality Tolerance Limits (QTLs), and analytical outputs. Support the evaluation of trends, data anomalies, protocol deviations, and performance metrics to detect potential quality or compliance issues. Document and report signals, findings, and recommendations within designated systems (e.g., CTMS, RBQM platform). Support study teams' understanding of the significance and root causes of centralized monitoring findings. Contribute to the development and maintenance of RBQM documentation, including: Centralized Monitoring Plans KRI and QTL threshold definitions SDV and SDR strategies Collaborate with Clinical Monitoring to support alignment of monitoring approaches with ICH-GCP E6 (R2/R3) and internal SOPs. Provide input on targeted monitoring actions, such as focused SDV, site

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