Junior Clinical Research Associate - Multi-Sponsored

IQVIA; Riyadh; On-site; SAR 70,000 - 120,000; Full time

Benefits offered by this job

Career growth resources

Flexible work schedules

Therapeutic knowledge programs

Excellent working environment

Attractive benefits package

Job summary

IQVIA Saudi Arabia is looking for talented and motivated team member to join our Multi-Sponsored team as junior CRA. At this position you will have the opportunity to put your passions to work in an environment designed to help you gain experience in a wide variety of therapeutic areas, and build a meaningful, strong career within our organization.

Under General Supervision, Your Responsibilities Will Include performing site visits, supporting subject recruitment, monitoring regulatory

Qualifications

• University degree in a scientific discipline or health care.
• Experience in Pharma Industry and/or Clinical Trials environment.
• Very good computer skills including MS Office.
• Excellent command of Arabic and English.
• Organizational, time management and problem-solving skills.
• Ability to establish and maintain effective working relationships with co-workers, managers and clients.
• Flexibility to travel.
• Driver’s license class B.

Responsibilities

• Performing site selection, initiation, monitoring and close-out visits.
• Supporting the development of a subject recruitment plan.
• Evaluating the quality and integrity of site practices per regulatory requirements.
• Managing progress by tracking regulatory submissions, recruitment, data query resolutions.
• Collaborating with experts at study sites and with client representatives.

Education

University degree in scientific discipline or health care

Tools

MS Office

Driver's license (Class B)

Job description

Associate Clinical Research Associate

IQVIA Saudi Arabia is looking for talented and motivated team member to join our Multi-Sponsored team as junior CRA. At this position you will have the opportunity to put your passions to work in an environment designed to help you gain experience in a wide variety of therapeutic areas, and build a meaningful, strong career within our organization.

Under General Supervision, Your Responsibilities Will Include

• Performing site selection, initiation, monitoring and close-out visits
• Supporting the development of a subject recruitment plan
• Evaluating the quality and integrity of site practices in accordance with regulatory requirements, i.e., Good Clinical Practice and International Conference on Harmonization guidelines
• Managing progress by tracking regulatory submissions, recruitment, case report form completion, and data query resolutions
• Collaborating with experts at study sites and with client representatives

Qualifications

• University degree in scientific discipline or health care
• Experience in Pharma Industry, and/or Clinical Trials environment
• Very good computer skills including MS Office
• Excellent command of Arabic and English language
• Organizational, time management and problem-solving skills
• Ability to establish and maintain effective working relationships with co-workers, managers, and clients
• Flexibility to travel
• Driver’s license class B

What You Can Expect

• Resources that promote your career growth
• Leaders that support flexible work schedules
• Programs to help you build your therapeutic knowledge
• Excellent working environment in a stabile, international, reputable company
• Attractive benefits package

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com

IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.