ZipRecruiter

Log In

1

Clinical Site Management Associate Jobs (NOW HIRING)

Alcanza Clinical Research

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 ...

Alcanza Clinical Research

Clinical Site Director

Decatur, GA · On-site

$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 ...

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 ...

AbbVie

Site Management Lead

North Chicago, IL · On-site

Influences and aligns within Clinical Development Operations, with other assigned Site Management leaders, and key stakeholders in assigned studies. If assigned as the study strategy leader, is a key ...

AbbVie

Site Management Lead

North Chicago, IL · On-site

$109K/yr

Influences and aligns within Clinical Development Operations, with other assigned Site Management leaders, and key stakeholders in assigned studies. If assigned as the study strategy leader, is a key ...

Accel Research Sites

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 ...

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 ...

AbbVie

Site Management Lead

North Chicago, IL

Influences and aligns within Clinical Development Operations, with other assigned Site Management leaders, and key stakeholders in assigned studies. If assigned as the study strategy leader, is a key ...

Allergan

Site Management Lead

Irvine, CA · On-site

Influences and aligns within Clinical Development Operations, with other assigned Site Management leaders, and key stakeholders in assigned studies. If assigned as the study strategy leader, is a key ...

Allergan

Site Management Lead

North Chicago, IL · On-site

Influences and aligns within Clinical Development Operations, with other assigned Site Management leaders, and key stakeholders in assigned studies. If assigned as the study strategy leader, is a key ...

previous pagenext page

Showing results 21-40

All JobsHealthcare JobsHospital JobsDirector Of Pharmacy JobsClinical Site Management Associate Jobs

Clinical Site Management Associate information

See salary details

$12

$31

$55

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

As of Sep 11, 2026, the average hourly pay for clinical site management associate 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.

What is a clinical site management associate?

Clinical Site Management Associates (CSMAs) are professionals in the clinical research industry who support the management and oversight of clinical trial sites. They assist with site selection, initiation, monitoring, and closure activities to ensure trials are conducted according to protocols, regulations, and Good Clinical Practice (GCP) guidelines. CSMAs often serve as a liaison between the sponsor, clinical research associates, and site staff, helping to resolve issues and maintain study timelines. Their work is vital in ensuring the quality and integrity of clinical research data.

What are the key skills and qualifications needed to thrive as a clinical site management associate, and why are they important?

To thrive as a Clinical Site Management Associate, you need a strong understanding of clinical trial processes, regulatory guidelines, and a bachelor's degree in life sciences or a related field. Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC) tools, and GCP certification is typically required. Strong organizational skills, attention to detail, and effective communication help you build solid relationships with site staff and ensure study compliance. These competencies are critical for ensuring the smooth execution of clinical trials, regulatory adherence, and high-quality data collection.

What are some common challenges faced by clinical site management associates, and how can they be addressed?

Clinical Site Management Associates often navigate challenges such as coordinating communication between site staff and sponsors, ensuring regulatory compliance, and managing multiple study sites simultaneously. To address these challenges, strong organizational skills, proactive problem-solving, and effective communication are essential. Many teams use project management tools and regular check-ins to track progress and resolve issues promptly. Engaging in ongoing training and collaborating closely with Clinical Research Associates and site coordinators can also help streamline processes and maintain study quality.

What is the difference between Clinical Site Management Associate vs Clinical Research Coordinator?

AspectClinical Site Management AssociateClinical Research Coordinator
CredentialsBachelor's degree often required; certifications like CCRP beneficialBachelor's degree typically required; certifications like CCRP advantageous
Work EnvironmentSupports site operations, manages regulatory compliance, liaises with sponsorsCoordinates study activities, enrolls participants, collects data
Employer & Industry UsagePharmaceutical companies, CROs, research sitesAcademic institutions, hospitals, research centers

The Clinical Site Management Associate focuses on overseeing site operations and regulatory compliance, while the Clinical Research Coordinator handles participant recruitment and data collection. Both roles require similar educational backgrounds and certifications, but their daily responsibilities and work environments differ slightly.

What states have the most Clinical Site Management Associate jobs?

States with the most job openings for Clinical Site Management Associate jobs include:

What are popular job titles related to Clinical Site Management Associate jobs?

For Clinical Site Management Associate jobs, the most frequently searched job titles are:

Infographic showing various Clinical Site Management Associate job openings in the United States as of September 2026, with employment types broken down into 1% As Needed, 82% Full Time, 15% Part Time, and 2% Contract. Highlights an 87% Physical, 2% Hybrid, and 11% Remote job distribution, with an average salary of $65,604 per year, or $31.5 per hour.

Clinical Site Director

Decatur, GA • On-site

Alcanza Clinical Research
51 - 200 employees
Learn more about Alcanza Clinical Researchexternal

$87K - $119K/yr

Full-time

Medical, Dental, Vision, Life, Retirement

Posted 10 days ago

Job description

Clinical Site Director
Department: Operations
Employment Type: Full Time
Location: Accel Research Sites - Decatur, GA
Reporting To: Adrienne Hilliard
Description
Alcanza is a growing multi-site, multi-phase clinical research company with a network of locations in AL, AZ, FL, GA, IL, MA, MI, MO, NV, VA, SC, TN, TX and Puerto Rico. We have established a strong presence across Phase I-IV studies and several therapeutic areas including vaccine, neurology, dermatology, psychiatry, and general medicine. Join us as we continue to grow.
The Clinical Site Director is responsible for driving operational performance for of the research site. Provides on-site oversight to help ensure execution and coordination of clinical research activities according to ICH guidelines, GCP, and FDA guidelines and follows company policies and procedures.
Key Responsibilities
Essential Job Duties:
  • Overall site management and leadership with a focus on driving site performance, enhancing efficiencies, pati,ent safety and protocol/GCP/regulatory compliance.
  • Collaborating with department leaders in Business Development, Patient Recruitment, Finance, and Budgets Contracts and Quality to coordinate delivery expectations, meet expected study milestones (such as site activation targets, enrollment targets, etc.), meet budgets, and delivery quality data to sponsors.
  • Reviewing the performance dashboards and other clinical trial systems to oversee site and patient activities, ensure proper staff coverage, and to ensure the data has been updated to reflect timely execution of all operational aspects (required visits/calls, duration, and frequency).
  • Overseeing resourcing allocations, site assignments and study team members' output and performance, to ensure study deliverables are on track, identifying risks to delivery or quality, and escalating any risks to clinical trial management deliverables (timeline, quality and budget).
  • Assisting with initial and ongoing trainings regarding protocol specificities, Case Report Form (CRF) completion, Standard Operating Procedures (SOPs), clinical plans and guidelines, and timelines for the study.
  • Ensuring adherence to standard operating procedures, good clinical practice (GCP), FDA regulations, and company policies and procedures.
  • Overseeing site staff assigned to the study and routinely assessing study-specific process and training compliance, CMP compliance, and identifies emerging risks.
  • Develop and support execution of corrective action plans at site and study level.
  • Overseeing people management activities including interviewing and selection, performance appraisals, job description preparation, employee counseling, career coaching and termination meetings. Managing site staff, proactively identify and resolve issues, and work to ensure successful site operations.
  • Overseeing all payroll, absence tracking/approvals, new hire orientation, and training per operational needs.
  • Collaborating with investigators to ensure patient safety and meeting client goals and timelines.
  • Employing strategic thinking and problem-solving skills to propose and implement risk mitigations.
  • Participating and presenting in management or site meetings.
  • Perform all other duties as required or assigned.

Skills, Knowledge and Expertise
Minimum Qualifications: A Bachelor's degree AND 5+ years of clinical research experience or an equivalent combination of education and experience is required. 2+ years of clinical research site management experience is required. Bi-lingual (English / Spanish) proficiency is preferred.
Required Skills:
  • Proficiency with computer applications such as Microsoft applications, email, electronic health records, web applications, and the ability to type proficiently (40+ wpm).
  • Must possess strong organizational, time management, problem solving, and project management skills to meet project deadlines.
  • Well-developed written and verbal communication skills.
  • Well-developed interpersonal and listening skills and the ability to work well independently as well as with co-workers, subjects, managers and external customers.
  • Ability to effectively handle multiple tasks and adapt to changes in workloads and priorities.
  • Must be professional, respectful of others, self-motivated, and have a strong work ethic.
  • Must possess a high degree of integrity and dependability.
  • Ability to work under minimal supervision, identify problems and implement solutions.
  • Ability to handle highly sensitive information in a confidential and professional manner, and in compliance with HIPAA guidelines.

Benefits
  • Full-time employees regularly scheduled to work at least 30 hours per week are benefits-eligible, with coverage starting on the first day of the month following date of hire.
  • Medical, dental, vision, life insurance, short and long-term disability insurance, health savings accounts, supplemental insurances, and a 401k plan with a safe harbor match are offered.

Apply