Certificate in Trial Participant Screening Protocols

-- viewing now

The Certificate in Trial Participant Screening Protocols is a comprehensive course designed to meet the growing industry demand for experts in clinical trial participant screening. This course emphasizes the importance of thorough participant screening, a critical aspect of successful clinical trials, by providing learners with in-depth knowledge of screening protocols and best practices.

4.5
Based on 5,211 reviews

7,382+

Students enrolled

GBP £ 140

GBP £ 202

Save 44% with our special offer

Start Now

About this course

Throughout the course, learners will develop essential skills in participant eligibility criteria, informed consent, and data management, ensuring they are well-equipped to contribute to the integrity and validity of clinical trials. As the biotechnology and pharmaceutical industries continue to expand, the need for qualified professionals with a deep understanding of trial participant screening protocols has never been greater. Earning this certificate will empower learners to advance their careers while making a significant impact on the future of healthcare and medical research.

100% online

Learn from anywhere

Shareable certificate

Add to your LinkedIn profile

2 months to complete

at 2-3 hours a week

Start anytime

No waiting period

Course Details

Introduction to Trial Participant Screening Protocols: Understanding the importance of screening protocols in clinical trials, including eligibility criteria, exclusion criteria, and the role of informed consent.
Pre-Screening Procedures: Learning about the initial steps in the screening process, such as reviewing medical histories, conducting interviews, and identifying potential participants.
Screening Evaluations: Exploring the various assessments used during the screening process, including physical examinations, laboratory tests, and imaging studies.
Data Management in Screening: Understanding the importance of accurate data collection and management during the screening process, including data entry, security, and confidentiality.
Ethical Considerations in Trial Participant Screening: Examining the ethical issues surrounding the screening process, such as informed consent, patient privacy, and the potential for bias.
Regulatory Compliance in Screening: Learning about the regulatory requirements for clinical trial screening protocols, including FDA regulations, ICH guidelines, and local laws.
Screening Process Improvement: Exploring strategies for improving the screening process, including the use of technology, standardization, and quality control measures.
Communication and Documentation in Screening: Understanding the importance of clear communication and documentation during the screening process, including with study sponsors, investigators, and participants.

Career Path

Roles in trial participant screening protocols involve managing and coordinating activities related to selecting eligible candidates for clinical trials. Key tasks include: * **Data Analysis:** Reviewing and analyzing applicant data to determine eligibility. * **Medical Background:** Understanding medical terminology and conditions to assess participant suitability. * **Communication:** Liaising with various stakeholders, including researchers, clinicians, and potential trial participants. * **Legal Knowledge:** Complying with legal and ethical regulations governing clinical trials. * **Technical Writing:** Documenting trial participant screening protocols and related materials. These roles are in demand in the UK, with competitive salary ranges depending on the specific position, organization, and level of experience. To excel in these roles, focus on building the necessary skills and staying updated on industry trends.

Entry Requirements

  • Basic understanding of the subject matter
  • Proficiency in English language
  • Computer and internet access
  • Basic computer skills
  • Dedication to complete the course

No prior formal qualifications required. Course designed for accessibility.

Course Status

This course provides practical knowledge and skills for professional development. It is:

  • Not accredited by a recognized body
  • Not regulated by an authorized institution
  • Complementary to formal qualifications

You'll receive a certificate of completion upon successfully finishing the course.

Why people choose us for their career

Loading reviews...

Frequently Asked Questions

What makes this course unique compared to others?

How long does it take to complete the course?

What support will I receive during the course?

Is the certificate recognized internationally?

What career opportunities will this course open up?

When can I start the course?

What is the course format and learning approach?

Course fee

MOST POPULAR
Fast Track: GBP £140
Complete in 1 month
Accelerated Learning Path
  • 3-4 hours per week
  • Early certificate delivery
  • Open enrollment - start anytime
Start Now
Standard Mode: GBP £90
Complete in 2 months
Flexible Learning Pace
  • 2-3 hours per week
  • Regular certificate delivery
  • Open enrollment - start anytime
Start Now
What's included in both plans:
  • Full course access
  • Digital certificate
  • Course materials
All-Inclusive Pricing • No hidden fees or additional costs

Get course information

We'll send you detailed course information

Pay as a company

Request an invoice for your company to pay for this course.

Pay by Invoice

Earn a career certificate

Sample Certificate Background
CERTIFICATE IN TRIAL PARTICIPANT SCREENING PROTOCOLS
is awarded to
Learner Name
who has completed a programme at
London College of Foreign Trade (LCFT)
Awarded on
05 May 2025
Blockchain Id: s-1-a-2-m-3-p-4-l-5-e
Add this credential to your LinkedIn profile, resume, or CV. Share it on social media and in your performance review.
SSB Logo

4.8
New Enrollment