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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
$5,750 - $6,150

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 for Drugs and Biologics

Prepare for regulatory affairs roles in drugs and biologics with hands-on, online training in U.S. and global requirements.

Duration
9 -15 Months
Cost
$3,800

Regulatory Affairs for Medical Devices

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

Duration
9 -15 Months
Cost
$4,100

Clinical Trials & Regulatory Affairs Courses

Classroom type:
Live Online
In-Person
Online
Hybrid
FPM-X402.33

CT: Biostatistical Approaches to Clinical Trial Design

Units
2.00
Cost
$525.00
Typically Offered
Winter, Summer
FPM-X406.85

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

Units
3.00
Cost
$645.00
Typically Offered
Fall, Spring, Summer
FPM-X401.73

CT: Drug Development Process

Units
3.00
Cost
$645.00
Typically Offered
Fall, Winter, Spring, Summer
FPM-X403.38

CT: Financial Management of Clinical Trials

Units
1.00
Cost
$325.00
Typically Offered
Fall, Winter, Spring, Summer
FPM-X402.04

CT: Good Clinical Practices

Units
3.00
Cost
$645.00
Typically Offered
Fall, Winter, Spring, Summer
FPM-X403.88

CT: Human Subjects Protection and IRBs

Units
2.00
Cost
$525.00
Typically Offered
Fall, Winter, Spring, Summer
FPM-X404.94

CT: Monitoring Oncology Trials

Units
3.00
Cost
$645.00
Typically Offered
Fall, Winter, Spring, Summer
FPM-X406.56

CT: Project Management in Clinical Trials

Units
3.00
Cost
$645.00
Typically Offered
Fall, Winter, Spring, Summer
FPM-X401.89

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

Units
3.00
Cost
$645.00
Typically Offered
Fall, Winter, Spring, Summer
FPM-X402.05

CT: Science of Clinical Trials Design

Units
3.00
Cost
$645.00
Typically Offered
Fall, Winter, Summer
FPM-X402.08

CT: Site and Investigator Recruitment

Units
1.00
Cost
$325.00
Typically Offered
Fall, Winter, Spring, Summer
FPM-X404.93

CT: Understanding Oncology

Units
3.00
Cost
$645.00
Typically Offered
Fall, Winter, Spring, Summer
BIOL-X403.24

Design Control for Medical Devices

Units
3.00
Cost
$745.00
BIOL-X400.85

Good Laboratory Practices

Units
2.00
Cost
$645.00
BIOL-X400.00

Good Manufacturing Practices

Units
3.00
Cost
$745.00
BIOL-X402.44

In Vitro Diagnostics Product Development

Units
2.00
Cost
$625.00
BIOL-X403.22

Overview of Regulatory Affairs for Medical Devices

Units
3.00
Cost
$745.00
BIOL-X403.26

Post Market Topics for Medical Devices

Units
3.00
Cost
$745.00
BIOL-X403.23

Quality Management Systems for Medical Devices

Units
3.00
Cost
$745.00
BIOL-X401.02

Regulatory Requirements for Drugs & Biologics

Units
2.50
Cost
$675.00
BIOL-X403.25

Regulatory Submissions for Medical Devices

Units
3.00
Cost
$745.00