Associate Clinical Study Manager: Drive Trial Excellence

Advanced Recruiting Partners

United States

On-site

USD 85,000 - 120,000

Full time

14 days+
Application generator

Turn this role into an interview — a resume and cover letter built around what this employer wants.

Get past ATS filters

Job summary

Advanced Recruiting Partners is seeking an Associate Clinical Study Manager (ACSM) to support planning, execution, and oversight of clinical trials, ensuring compliance with protocols, SOPs, and regulatory requirements.

You will collaborate with cross-functional teams, CRAs, sites, and vendors to manage timelines, enrollment, budgets, TMF accuracy, and regulatory submissions, while contributing to inspection readiness and risk mitigation.

Qualifications

  • Strong knowledge of clinical trial processes and GCP regulations.
  • Experience with CTMS and electronic Trial Master File (eTMF) systems.
  • Excellent organizational, project coordination, and communication skills.
  • Ability to manage multiple priorities in a fast-paced biotech environment.

Responsibilities

  • Support planning, implementing, and managing clinical trials.
  • Oversee site selection, feasibility, and site initiation.
  • Track enrollment, milestones, and timelines.
  • Monitor study performance metrics and escalate risks.
  • Serve as a liaison with CRAs, sites, CROs, and vendors.
  • Maintain TMF and assist in regulatory submissions and audits.
  • Provide status updates to internal stakeholders.
  • Support inspection readiness for regulatory authorities.

Skills

Clinical trial processes & GCP
CTMS & eTMF experience
Organizational & project coordination
Communication skills
Biotech/pharma/CRO experience

Education

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

Tools

CTMS
eTMF

Job description

Advanced Recruiting Partners is seeking an Associate Clinical Study Manager (ACSM) to support planning, execution, and oversight of clinical trials, ensuring compliance with protocols, SOPs, and regulatory requirements.

You will collaborate with cross-functional teams, CRAs, sites, and vendors to manage timelines, enrollment, budgets, TMF accuracy, and regulatory submissions, while contributing to inspection readiness and risk mitigation.

Get your free, confidential resume review.
or drag and drop your file here.
Similar jobs

Similar jobs worth comparing

Associate Clinical Study Manager
Associate Clinical Study Manager

Advanced Recruiting Partners • United States

On-site
USD 85,000 - 120,000
Senior Clinical Trial Manager, Clinical Operations
Senior Clinical Trial Manager, Clinical Operations

ADP, Inc. • San Diego (CA)

On-site
USD 150,000 - 165,000
Hybrid Associate Clinical Study Manager – Global Trials
Hybrid Associate Clinical Study Manager – Global Trials

Worldwide • San Antonio (TX), Northern (KY)

Hybrid
USD 28,000 - 55,000
Clinical Trials Site Manager
Clinical Trials Site Manager

Care Access • Town of Brandon (NY)

On-site
USD 80,000 - 110,000
PTO and company holidays
Medical, dental and vision insurance
Health Savings Account (HSA) and Flex
+2
Clinical Trial Associate
Clinical Trial Associate

Tech Observer • Paramus (NJ)

Hybrid
USD 60,000 - 80,000
Clinical Trial Manager
Clinical Trial Manager

Kelly Science, Engineering, Technology & Telecom • United States

On-site
USD 80,000 - 110,000
Clinical Trial Manager: Lead Study Delivery & Compliance
Clinical Trial Manager: Lead Study Delivery & Compliance

Cognitive Research Corporation • United States

On-site
USD 90,000 - 130,000
Clinical Study Lead - Trials & Compliance
Clinical Study Lead - Trials & Compliance

Dm Clinical Research Group • Philadelphia

On-site
USD 90,000 - 130,000
Clinical Trial Manager/Senior Clinical Trial Manager - CNS
Clinical Trial Manager/Senior Clinical Trial Manager - CNS

Cognitive Research Corporation • United States

On-site
USD 90,000 - 130,000
Senior Clinical Trial Manager
Senior Clinical Trial Manager

Brio Group • California (MO)

On-site
USD 80,000 - 120,000