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Associate Clinical Site Manager Jobs (NOW HIRING)

Accel Research Sites

Clinical Site Director

Decatur, GA · On-site

$87K - $119K/yr

Clinical Site Director Department: Operations Employment Type: Full Time Location: Accel Research ... Overall site management and leadership with a focus on driving site performance, enhancing ...

Socket.dev

Clinical Site Director

Woodstock, GA · On-site

$72K - $98K/yr

Clinical Site Director Department: Operations Employment Type: Full Time Location: North Georgia ... Overall site management and leadership with a focus on driving site performance, enhancing ...

Scorpion Therapeutics

Act as primary site contact/site manager across all phases of a clinical research study for ... Education/experience: Associate's degree (or equivalent) + 5+ years healthcare experience ...

Alcanza

Clinical Site Director

Decatur, GA

$78K - $106K/yr

The Clinical Site Director is responsible for driving operational performance for of the research ... Overall site management and leadership with a focus on driving site performance, enhancing ...

Alcanza

Clinical Site Director

Woodstock, GA · On-site

$72K - $98K/yr

The Clinical Site Director is responsible for driving operational performance for of the research ... Overall site management and leadership with a focus on driving site performance, enhancing ...

Jobtailor

Clinical Site Representative

Phoenix, AZ · On-site

Organize and manage required preceptor, student, and faculty training events * Increase ... Clinical Site Development * Contract Negotiation * Communication Skills * Organizational Skills

TriMedx, LLC

Associates look forward to coming to work each day* Every associate matters and makes a difference ... The Site Manager Clinical Engineering leads clinical engineering initiatives to provide superior ...

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How much do associate clinical site manager jobs pay per hour?

As of Sep 10, 2026, the average hourly pay for associate clinical site manager in the United States is $31.54, according to ZipRecruiter salary data. Most workers in this role earn between $21.15 and $41.59 per hour, depending on experience, location, and employer.

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Infographic showing various Associate Clinical Site Manager job openings in the United States as of July 2026, with employment types broken down into 88% Full Time, 11% Part Time, and 1% Contract. Highlights an 83% Physical, 2% Hybrid, and 15% Remote job distribution, with an average salary of $65,604 per year, or $31.5 per hour.

Associate Clinical Study Manager

San Antonio, TX • On-site

Worldwide Clinical Trials
Scientific Research and Development Services • 10K+ employees
Learn more about Worldwide Clinical Trialsexternal

Other

This job post has expired today. Applications are no longer accepted.

Job description

What the Associate Clinical Study Manager does at Worldwide


The Associate, Clinical Study Manager will be responsible for the site-level monitoring activities of on one or more allocated Phase I through IV Clinical Trials that may be local, regional, or global in scope. Supports the CSM with directing the technical, financial, and operational aspects to ensure the successful completion of the clinical trials. Works with functional area leads to identify and evaluate essential project prerequisites. The ACSM cooperates with the CSM to ensure all project deliverables meet client’s time/quality/cost expectations.


What you will do


  • Coordinate study monitoring visits, to include (but not limited to): ensuring the monitor has access to the relevant electronic systems, reserving monitoring space, assembling study documents for CRA review, and ensuring all follow-up action items are completed in a timely manner.
  • Work collaboratively with other clinic departments to ensure all queries are answered in a timely manner.
  • Manage and store signed approval forms for Clinical Lab, PK processing, Clinspark Go live, and Clinspark training and access request forms from clients.
  • Coordinate and collate signature forms for SIV attendance, logistics meetings, and any other protocol training related meetings, file in the appropriate study folder.
  • Ensure staff training is documented in the appropriate study files on the study protocol and other related processes, adhere to professional standards and to SOPs as well as current Good Clinical Practice (GCP) and applicable local regulations.
  • Facilitate shipment of samples to bioanalytical labs for analysis per the study timeline and/or client request.


What you will bring to the role


  • Excellent communication, planning, and organizational skills.
  • Sense of urgency and ability to be adaptable in a fast-paced and rapidly changing environment.
  • Self-motivated and excellent problem-solving skills.
  • Ability to work independently.
  • Ability to negotiate and liaise with clients in a professional manner.
  • Must have satisfactory customer service skills.


Your experience


  • Bachelor’s Degree (Life Sciences or Health preferred) or 4 years clinical research experience Or Associates Degree with 2 years clinical research experience.
  • Min 1 year as a Clinical Research Coordinator preferred


Apply