Clinical Research Associate (level dependent on experience)

Ctifacts; Riyadh; On-site; SAR 180,000 - 240,000; Full time

Job summary

CTI Clinical Trial and Consulting Services in Riyadh, Saudi Arabia, seeks a Clinical Research Associate to support successful conduct of trials and act as the main site contact for CTI.

Responsibilities include performing initiation, monitoring and close-out visits, supporting regulatory start-up activities, ensuring data integrity and timelines, and participating in global project meetings; requires 2–3 years of CRA experience and strong ICH-GCP knowledge.

Qualifications

• 2–3 years of clinical research experience as a CRA or related profession.
• Life science background.
• Excellent knowledge of ICH-GCP and regulatory requirements.

Responsibilities

• Conduct evaluation, initiation, monitoring and close out visits.
• Assist with regulatory and study start-up activities including contract and budget negotiations.
• Ensure clinical data integrity and meet study timelines.
• Provide ongoing updates and support to project management.
• Attend global project meetings including investigator meetings and global team teleconferences.
• Complete assigned training programs in drug development processes, therapeutic areas, GCPs and any applicable local regulatory requirements.

Skills

CRA experience

Life science background

ICH-GCP knowledge

Job description

Position:Clinical Research Associate (level dependent on experience)

Location: Riyadh, Saudi Arabia

Job Id:080-22 c

# of Openings:1

Clinical Research Associate (level dependent on experience)

Job Purpose/Summary

As a CRA you will be responsible for the successful conduct of clinical trials and serve as the main contact for the investigative site by representing CTI in a professional manner.

What You’ll Do

• Conduct evaluation, initiation, monitoring and close out visits
• Assist with regulatory and study start-up activities including contract and budget negotiations
• Ensure clinical data integrity and meet study timelines
• Provide ongoing updates and support to project management
• Attend global project meetings including investigator meetings and global team teleconferences
• Complete assigned training programs in drug development processes, therapeutic areas, Good Clinical Practices (GCPs) and any applicable local regulatory requirements.

What You Bring

• 2 - 3 years of clinical research experience as a CRA or related profession
• Life science background
• Excellent knowledge in ICH-GCP and regulatory requirement

Why CTI?

At CTI, we recognize that our people are what make our company successful. Our work moves medicine forward.

For that reason, we treat our team members with the respect they deserve, and our numbers show it:

• We support career progression – We believe in promoting from within and we have a structured mentoring program and program for recent graduates to provide the support employees need to move forward
• We value education and training – We provide tuition assistance, partner with universities and colleges to create programs in our field, and have a dedicated training department
• We value our people - We have never had a layoff in our three decade history and we guaranteed full pay for our employees during the COVID-19 shut-down regardless of the number of hours worked. We support a work-life balance and the importance of time with family by offering generous vacation time, a hybrid work from home schedule, and paid parental leave.
• We think globally and act locally – With employees across 60 countries, we have global reach but maintain culture and connections to the local communities in which we work. Our CTI Cares Committees are dedicated to ensuring the CTI culture and values translate around the world.
• We are looking toward the future – We have had a consistent double-digit growth rate over the last decade, invest in cutting-edge technology, and pride ourselves on our average annual retention rate of 95%, which is much higher than many other CROs
• Our work makes a difference – We focus our work on treatments for chronically and critically-ill patients, who are depending on us to bring these life-changing therapies to market

CTI Clinical Trial and Consulting Services

Filipa Magalhães

www.ctifacts.com