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Healthcare

Clinical Trials & Regulatory Affairs

Get the training to conduct clinical trials and fulfill the educational requirements to become a CRA or CRC.

Join the thriving clinical trials market
Conducting clinical trials is essential to ensure the safety and efficacy of new drugs, biologics and medical devices. The demand for highly trained professionals to coordinate and manage clinical trials for the local, national and international biomedical and biotech communities continues to grow rapidly. By learning key concepts, guidelines, regulations and best practices, professionals gain the skills needed to become part of an active workforce and fulfill the requirements to become a CRA or CRC through ACRP, or CRP through SoCRA.

Clinical Trials & Regulatory Affairs Programs & Certificates

Classroom type:
Live Online
In-Person
Online
Hybrid

Biotechnology Project Management

Gain specialized skills to manage biotech projects from discovery to launch in this online certificate for science and pharma professionals.

Duration
9 Months
Cost
$6,240

Clinical Trials Design and Management Program

Since 1997, this program has trained clinical trial professionals at all levels and meets ACRP and SoCRA education requirements for certification.

Duration
6 - 24 Months
Cost
$5,100 - $5,700

Quality Assurance and Control

For chemists, biochemists, and biologists new to QA/QC in the pharmaceutical and biologics industry.

Duration
12-18 months
Cost
$3,750

Regulatory Affairs Essentials

A dynamic career at the intersection of science, business, and public service—focused on saving lives.

Duration
9 -15 Months
Cost
$3,580

Regulatory Affairs for Medical Devices

Gain the skills to navigate regulations and bring medical devices from concept to market.

Duration
9 -15 Months
Cost
$3,850

Clinical Trials & Regulatory Affairs Courses

Classroom type:
Live Online
In-Person
Online
Hybrid
FPM-40218

CT: Data Management Systems for Sponsors of Clinical Trials

Units
2.00
Cost
$525.00
FPM-40685

CT: Documents in Drug Development: Writing Protocols, Reports, Summaries, Submissions, and Disclosures

Units
3.00
Cost
$645.00
FPM-40173

CT: Drug Development Process

Units
3.00
Cost
$645.00
FPM-40338

CT: Financial Management of Clinical Trials

Units
1.00
Cost
$325.00
FPM-40204

CT: Good Clinical Practices

Units
3.00
Cost
$645.00
FPM-40388

CT: Human Subjects Protection and IRBs

Units
2.00
Cost
$525.00
FPM-40494

CT: Monitoring Oncology Trials

Units
3.00
Cost
$645.00
FPM-40233

CT: Practical Clinical Statistics for the Non-Statistician

Units
2.00
Cost
$525.00
FPM-40656

CT: Project Management in Clinical Trials

Units
3.00
Cost
$645.00
FPM-40189

CT: Regulation of Drugs, Biologics, Devices, and Diagnostics

Units
3.00
Cost
$645.00
FPM-40205

CT: Science of Clinical Trials Design

Units
3.00
Cost
$645.00
FPM-40208

CT: Site and Investigator Recruitment

Units
1.00
Cost
$325.00
FPM-40493

CT: Understanding Oncology

Units
3.00
Cost
$645.00
BIOL-40324

Design Control for Medical Devices

Units
3.00
Cost
$745.00
BIOL-40201

Good Documentation Practices

Units
3.00
Cost
$745.00
BIOL-40085

Good Laboratory Practices

Units
2.00
Cost
$645.00
BIOL-40000

Good Manufacturing Practices

Units
3.00
Cost
$745.00
BIOL-40244

In Vitro Diagnostics Product Development

Units
2.00
Cost
$625.00
BIOL-40322

Overview of Regulatory Affairs for Medical Devices

Units
3.00
Cost
$745.00
BIOL-40326

Post Market Topics for Medical Devices

Units
3.00
Cost
$745.00
BIOL-40323

Quality Management Systems for Medical Devices

Units
3.00
Cost
$745.00
BIOL-40101

Regulatory Compliance for Drugs & Biologics

Units
2.00
Cost
$645.00
BIOL-40102

Regulatory Requirements for Drugs & Biologics

Units
2.50
Cost
$675.00
BIOL-40325

Regulatory Submissions for Medical Devices

Units
3.00
Cost
$745.00