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Clinical Project Associate Jobs in Three Rivers, MI

Patient Access Coordinator

Granger, IN · On-site

$15.25 - $19.25/hr

Ensure office and clinical supply inventory is current, supplies are ordered in a timely manner ... projects as directed. ORGANIZATIONAL RESPONSIBILITIES Associate complies with the following ...

Patient Access Coordinator

Granger, IN · On-site

$15.25 - $19.25/hr

Ensure office and clinical supply inventory is current, supplies are ordered in a timely manner ... projects as directed. ORGANIZATIONAL RESPONSIBILITIES Associate complies with the following ...

Patient Access Coordinator

Granger, IN · On-site

$15.25 - $19.25/hr

Ensure office and clinical supply inventory is current, supplies are ordered in a timely manner ... projects as directed. ORGANIZATIONAL RESPONSIBILITIES Associate complies with the following ...

Physical Therapist

Three Rivers, MI · On-site

$1.5K - $1.9K/wk

Clinical Practice * Completes appropriate assessment per physician's orders and diagnosis ... projects as assigned. ORGANIZATIONAL RESPONSIBILITIES Associate complies with the following ...

Physical Therapist

Three Rivers, MI · On-site

$1.5K - $1.9K/wk

Clinical Practice * Completes appropriate assessment per physician's orders and diagnosis ... projects as assigned. ORGANIZATIONAL RESPONSIBILITIES Associate complies with the following ...

Physical Therapist

Three Rivers, MI

$1.5K - $1.9K/wk

Clinical Practice * Completes appropriate assessment per physician's orders and diagnosis ... projects as assigned. ORGANIZATIONAL RESPONSIBILITIES Associate complies with the following ...

Physical Therapist

Three Rivers, MI

$1.5K - $1.9K/wk

Clinical Practice * Completes appropriate assessment per physician's orders and diagnosis ... projects as assigned. ORGANIZATIONAL RESPONSIBILITIES Associate complies with the following ...

Occupational Therapist

Elkhart, IN · On-site

$38.25 - $50.25/hr

Clinical Practice: * Completes appropriate assessment per physician's orders and diagnosis ... projects as assigned. ORGANIZATIONAL RESPONSIBILITIES Associate complies with the following ...

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Clinical Project Associate information

See Three Rivers, MI salary details

$11

$29

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How much do clinical project associate jobs pay per hour?

As of Jul 14, 2026, the average hourly pay for clinical project associate in Three Rivers, MI is $29.09, according to ZipRecruiter salary data. Most workers in this role earn between $19.52 and $38.37 per hour, depending on experience, location, and employer.

What is a Clinical Project Associate?

A Clinical Project Associate (CPA) is a professional who supports the planning, execution, and management of clinical trials in the pharmaceutical, biotechnology, or medical device industries. Their responsibilities often include coordinating study documentation, assisting with regulatory submissions, tracking project timelines, and facilitating communication among study teams. CPAs play a crucial role in ensuring that clinical trials are conducted efficiently, ethically, and in compliance with regulatory standards. They work closely with clinical project managers, research associates, and other team members to help bring new therapies and treatments to market.

What are the typical responsibilities of a Clinical Project Associate in supporting clinical trial operations?

As a Clinical Project Associate, you will play a vital role in ensuring the smooth execution of clinical trials by handling administrative and logistical tasks. Your responsibilities often include maintaining study documentation, coordinating meetings, tracking project timelines, and supporting communication between internal teams and external partners such as clinical sites and vendors. You may also assist with regulatory submissions and help monitor compliance with study protocols. This position offers excellent exposure to the clinical research process and can be a stepping stone to more advanced roles within clinical operations.

What are the key skills and qualifications needed to thrive as a Clinical Project Associate, and why are they important?

To thrive as a Clinical Project Associate, you need a background in life sciences or a related field, attention to detail, and strong organizational skills. Familiarity with clinical trial management systems (CTMS), regulatory documentation, and tools like Microsoft Office is typically required. Excellent communication, teamwork, and time management abilities help professionals excel in supporting project coordination. These skills are crucial for ensuring regulatory compliance, smooth project execution, and effective collaboration within clinical research teams.

What is the difference between Clinical Project Associate vs Clinical Research Coordinator?

AspectClinical Project AssociateClinical Research Coordinator
CredentialsBachelor's degree often required; certifications like CCRP beneficialBachelor's degree in health or related field; certifications like CCRP common
Work EnvironmentTypically works with project teams, sponsors, and CROs in clinical trial settingsWorks directly with patients, investigators, and site staff at clinical trial sites
Employer & IndustryPharmaceutical companies, CROs, biotech firmsHospitals, clinics, research sites
Search & Comparison IntentHigh overlap in responsibilities and certificationsSimilar roles but more patient-facing

The Clinical Project Associate primarily supports clinical trial management from a project perspective, working with sponsors and CROs. In contrast, the Clinical Research Coordinator focuses on patient interactions and site management. Both roles require similar educational backgrounds and certifications, but their work environments and daily tasks differ significantly.

Medical Lab Scientist

Medical Lab Scientist

Beacon Health System

Plainwell, MI • On-site

Full-time

Re-posted 28 days ago


Beacon Health System rating

6.7

Company rating: 6.7 out of 10

Based on 142 frontline employees who took The Breakroom Quiz

525th of 884 rated healthcare providers


Job description

Full time. 40 hours per week. Night shift. Rotating weekends/holidays
 
 
 
Performs routine diagnostic and analytic testing of laboratory specimens independently.
Responsibilities:
Performs, validates, interprets, documents and reports laboratory test results. May collect and process specimens.
Performs instrument maintenance and troubleshooting. Executes and evaluates quality control and quality assurance procedures. Documents and reports as required by regulatory agencies.
Understands and participates in all aspects of clinical laboratory testing; pre-analytical, analytical, and post-analytical. Anticipates and maintains required supplies for uninterrupted testing.
Assists with data collection or special projects as assigned.
Aides in documentation, evaluation and submission of all required laboratory, departmental and staff statistics/reports.
Trains and mentors Medical Lab Technicians (MLTs) , new associates and students. Medical Tech Required: N Preferred: Y, Medical Technologist (ASCP) Required: N Preferred: Y, LIC Medical Lab Scientist (ASCP) Required: N Preferred: Y, Bachelor's degree in medical technology, medical laboratory scientist, human sciences or education qualifications as stated per CLIA requirements. None required. EDUCATION Diploma Required: N Preferred: N"

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