25 Medical Research jobs in Saudi Arabia

Experienced Clinical Research Associate Sponsor-dedicated page is loadedExperienced Clinical Research Associate Sponsor-dedicated Apply locations Riyadh, Saudi Arabia time type Full time posted on Posted Yesterday job requisition id R1455607

Job Overview
Perform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol, applicable regulations and guidelines, and sponsor requirements.

Essential Functions
• Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with contracted scope of work and Good Clinical Practice.
• Work with sites to adapt, drive, and track subject recruitment plan in line with project needs to enhance predictability.
• Administer protocol and related study training to assigned sites and establish regular lines of communication with sites to manage ongoing project expectations and issues.
• Evaluate the quality and integrity of study site practices related to the proper conduct of the protocol and adherence to applicable regulations. Escalate quality issues as appropriate.
• Manage the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and enrollment, case report form (CRF) completion and submission, and data query generation and resolution. May support start-up phase.
• Ensure copies/originals (as required) site documents are available for filing in the Trial Master File (TMF) and verify that the Investigator's Site File (ISF) is maintained in accordance with GCP and local regulatory requirements.
• Create and maintain appropriate documentation regarding site management, monitoring visit findings and action plans by submitting regular visit reports, generating follow-up letters and other required study documentation.
• Collaborate and liaise with study team members for project execution support as appropriate.
• If applicable, may be accountable for supporting development of project subject recruitment plan on a per site basis.
• If applicable, may be accountable for site financial management according to executed clinical trial agreement and retrieve invoices according to local requirement.

Qualifications
• High School Diploma or equivalent Degree in scientific discipline or health care preferred.
• Requires at least 2 years of year of on-site monitoring experience.
• Equivalent combination of education, training and experience may be accepted in lieu of degree.
• Good knowledge of, and skill in applying, applicable clinical research regulatory requirements.
• i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines.
• Good therapeutic and protocol knowledge as provided in company training.
• Computer skills including proficiency in use of Microsoft Word, Excel and PowerPoint and use of a laptop computer and iPhone and iPad (where applicable).
• Written and verbal communication skills including good command of Arabic and English language.
• Organizational and problem-solving skills.
• Effective time and financial management skills.
• Ability to establish and maintain effective working relationships with coworkers, managers, and clients.

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

Similar Jobs (1) Experienced Clinical Trial Assistant locations Riyadh, Saudi Arabia time type Full time posted on Posted Yesterday

#J-18808-Ljbffr

Job Overview
Perform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol, applicable regulations and guidelines, and sponsor requirements.

Essential Functions
• Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with contracted scope of work and Good Clinical Practice.
• Work with sites to adapt, drive, and track subject recruitment plan in line with project needs to enhance predictability.
• Administer protocol and related study training to assigned sites and establish regular lines of communication with sites to manage ongoing project expectations and issues.
• Evaluate the quality and integrity of study site practices related to the proper conduct of the protocol and adherence to applicable regulations. Escalate quality issues as appropriate.
• Manage the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and enrollment, case report form (CRF) completion and submission, and data query generation and resolution. May support start-up phase.
• Ensure copies/originals (as required) site documents are available for filing in the Trial Master File (TMF) and verify that the Investigator's Site File (ISF) is maintained in accordance with GCP and local regulatory requirements.
• Create and maintain appropriate documentation regarding site management, monitoring visit findings and action plans by submitting regular visit reports, generating follow-up letters and other required study documentation.
• Collaborate and liaise with study team members for project execution support as appropriate.
• If applicable, may be accountable for supporting development of project subject recruitment plan on a per site basis.
• If applicable, may be accountable for site financial management according to executed clinical trial agreement and retrieve invoices according to local requirement.

Qualifications
• High School Diploma or equivalent Degree in scientific discipline or health care preferred.
• Requires at least 2 years of year of on-site monitoring experience.
• Equivalent combination of education, training and experience may be accepted in lieu of degree.
• Good knowledge of, and skill in applying, applicable clinical research regulatory requirements.
• i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines.
• Good therapeutic and protocol knowledge as provided in company training.
• Computer skills including proficiency in use of Microsoft Word, Excel and PowerPoint and use of a laptop computer and iPhone and iPad (where applicable).
• Written and verbal communication skills including good command of Arabic and English language.
• Organizational and problem-solving skills.
• Effective time and financial management skills.
• Ability to establish and maintain effective working relationships with coworkers, managers, and clients.

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

#J-18808-Ljbffr

Experienced Clinical Research Associate Sponsor-dedicated page is loaded Experienced Clinical Research Associate Sponsor-dedicated Apply locations Riyadh, Saudi Arabia time type Full time posted on Posted Yesterday job requisition id R1455607

Job Overview
Perform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol, applicable regulations and guidelines, and sponsor requirements.

Essential Functions
• Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with contracted scope of work and Good Clinical Practice.
• Work with sites to adapt, drive, and track subject recruitment plan in line with project needs to enhance predictability.
• Administer protocol and related study training to assigned sites and establish regular lines of communication with sites to manage ongoing project expectations and issues.
• Evaluate the quality and integrity of study site practices related to the proper conduct of the protocol and adherence to applicable regulations. Escalate quality issues as appropriate.
• Manage the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and enrollment, case report form (CRF) completion and submission, and data query generation and resolution. May support start-up phase.
• Ensure copies/originals (as required) site documents are available for filing in the Trial Master File (TMF) and verify that the Investigator's Site File (ISF) is maintained in accordance with GCP and local regulatory requirements.
• Create and maintain appropriate documentation regarding site management, monitoring visit findings and action plans by submitting regular visit reports, generating follow-up letters and other required study documentation.
• Collaborate and liaise with study team members for project execution support as appropriate.
• If applicable, may be accountable for supporting development of project subject recruitment plan on a per site basis.
• If applicable, may be accountable for site financial management according to executed clinical trial agreement and retrieve invoices according to local requirement.

Qualifications
• High School Diploma or equivalent Degree in scientific discipline or health care preferred.
• Requires at least 2 years of year of on-site monitoring experience.
• Equivalent combination of education, training and experience may be accepted in lieu of degree.
• Good knowledge of, and skill in applying, applicable clinical research regulatory requirements.
• i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines.
• Good therapeutic and protocol knowledge as provided in company training.
• Computer skills including proficiency in use of Microsoft Word, Excel and PowerPoint and use of a laptop computer and iPhone and iPad (where applicable).
• Written and verbal communication skills including good command of Arabic and English language.
• Organizational and problem-solving skills.
• Effective time and financial management skills.
• Ability to establish and maintain effective working relationships with coworkers, managers, and clients.

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

Similar Jobs (1) Experienced Clinical Trial Assistant locations Riyadh, Saudi Arabia time type Full time posted on Posted Yesterday #J-18808-Ljbffr

**Job Overview**
Perform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol, applicable regulations and guidelines, and sponsor requirements.
**Essential Functions**
- Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with contracted scope of work and Good Clinical Practice.
- Work with sites to adapt, drive, and track subject recruitment plan in line with project needs to enhance predictability.
- Administer protocol and related study training to assigned sites and establish regular lines of communication with sites to manage ongoing project expectations and issues.
- Evaluate the quality and integrity of study site practices related to the proper conduct of the protocol and adherence to applicable regulations. Escalate quality issues as appropriate.
- Manage the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and enrollment, case report form (CRF) completion and submission, and data query generation and resolution. May support start-up phase.
- Ensure copies/originals (as required) site documents are available for filing in the Trial Master File (TMF) and verify that the Investigator's Site File (ISF) is maintained in accordance with GCP and local regulatory requirements.
- Create and maintain appropriate documentation regarding site management, monitoring visit findings and action plans by submitting regular visit reports, generating follow-up letters and other required study documentation.
- Collaborate and liaise with study team members for project execution support as appropriate.
- If applicable, may be accountable for supporting development of project subject recruitment plan on a per site basis.
- If applicable, may be accountable for site financial management according to executed clinical trial agreement and retrieve invoices according to local requirement.
**Qualifications**
- High School Diploma or equivalent Degree in scientific discipline or health care preferred.
- Requires at least 2 years of year of on-site monitoring experience.
- Equivalent combination of education, training and experience may be accepted in lieu of degree.
- Good knowledge of, and skill in applying, applicable clinical research regulatory requirements.
- i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines.
- Good therapeutic and protocol knowledge as provided in company training.
- Computer skills including proficiency in use of Microsoft Word, Excel and PowerPoint and use of a laptop computer and iPhone and iPad (where applicable).
- Written and verbal communication skills including good command of Arabic and English language.
- Organizational and problem-solving skills.
- Effective time and financial management skills.
- Ability to establish and maintain effective working relationships with coworkers, managers, and clients.
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 is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide.
To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere. Thank you for your interest in growing your career with us.
EEO Minorities/Females/Protected Veterans/Disabled

If you want to do your next step as a CRA, this is your chance!

You’ll have training and development to plan and progress your career in the direction you choose. And you won’t do it alone – you will have dedicated mentoring and receive structured quarterly reviews on performance, promotion and bonus awards.

While Projects Vary, Your Typical Responsibilities Might Include

• Performing site selection, initiation, monitoring and close-out visits, plus maintaining appropriate documentation
• Supporting the development of a subject recruitment plan
• Establishing regular lines of communication plus administering protocol and related study training to assigned sites
• Evaluating the quality and integrity of site practices – escalating quality issues as appropriate
• Managing progress by tracking regulatory submissions, recruitment, case report form (CRF) completion, and data query resolution

You will need to be comfortable collaborating and communicating with a variety of colleagues and customers. Ideally, you will also have a good basic knowledge of applicable clinical research regulatory requirements.


You Should Have

• A Bachelor's degree in a health care or other scientific discipline or educational equivalent
• At least 1,5 - 2 years of on-site monitoring experience
• Fluent in Arabic and English language
• Good written and verbal communication skills including good command of English language
• Requires frequent travel to sites
• Flexible about location, but location must have good connectivity to travel
• Homebased

If you want to make an impact in the global research market, where we are working to make a real difference in patient health, we ask you to apply now and join our team .
Connect to great opportunity

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

#J-18808-Ljbffr

If you want to do your next step as a CRA, this is your chance!
You'll have training and development to plan and progress your career in the direction you choose. And you won't do it alone - you will have dedicated mentoring and receive structured quarterly reviews on performance, promotion and bonus awards.
**While Projects Vary, Your Typical Responsibilities Might Include**
+ Performing site selection, initiation, monitoring and close-out visits, plus maintaining appropriate documentation
+ Supporting the development of a subject recruitment plan
+ Establishing regular lines of communication plus administering protocol and related study training to assigned sites
+ Evaluating the quality and integrity of site practices - escalating quality issues as appropriate
+ Managing progress by tracking regulatory submissions, recruitment, case report form (CRF) completion, and data query resolution
You will need to be comfortable collaborating and communicating with a variety of colleagues and customers. Ideally, you will also have a good basic knowledge of applicable clinical research regulatory requirements.
**You Should Have**
+ A Bachelor's degree in a health care or other scientific discipline or educational equivalent
+ At least 1,5 - 2 years of on-site monitoring experience
+ Fluent in Arabic and English language
+ Good written and verbal communication skills including good command of English language
+ Requires frequent travel to sites
+ Flexible about location, but location must have good connectivity to travel
+ Homebased
If you want to make an impact in the global research market, where we are working to make a real difference in patient health, we ask you to **apply now and join our team** .
**Connect to** _great opportunity_
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 is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide.
To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere. Thank you for your interest in growing your career with us.
EEO Minorities/Females/Protected Veterans/Disabled

**Role Summary**:Manage the execution of the assigned clinical studies, from initiation through to

closeout. Ensure that all clinical study management and project deliverables are completed, ensuring

quality deliverables on time and in accordance with SOPs, policies and practices.

**What we Offer**:

- Excellent salary and benefits package
- Company car or car allowance
- Depending on the model, home-based is a possibility
- Flexible working hours in a home-based role
- As a CRA, you will receive a company iPad and have use of key developments such as site visit apps, visit reporting apps which allow CRAs to do their day to day job more efficiently!
- We invest in keeping our teams stable, so workload is consistent
- We offer genuine career development opportunities for those who want to grow as part of the organization
- We give the chance to work on cutting edge medicines, right at the forefront of new medicine development
**Role Details**:

- Working in partnership with a single-sponsor
- On site between 6 and 9 days per month, dependent on the sponsor
- All CRAs and SCRAs are allocated a dedicated IQVIA Line Manager
- Permanent employment contract
- Fantastic work/life balance - flexible working within the core hours of 10 am to 4 pm
- Sponsor model has reduced travel (approx. 30% or less) due to using ‘Fit for Purpose Monitoring’ which incorporates remote monitoring therefore there is less need for on-site visits

**Responsibilities**:

- Site management and monitoring activities across the Turkey
Provide protocol and study training to the assigned sites
- Create and maintain monitoring visit reports and action plans
- If appropriate, co-monitor, train and mentor junior members of the team

**Qualifications**:

- Computer literacy required, including well-developed computer skills in MS Word and Excel
- program experience preferred
Knowledge of procedures for monitoring clinical trials, GCP and medical terminology preferred, but not mandatory
- Demonstrated good problem solving and organizational skills, able to handle and prioritize multiple tasks
- Able to perform assigned task with mínimal direct supervision by Line Manager or Clinical Lead
Demonstrated good problem solving
- Able to handle and prioritize multiple tasks/assignments
- Demonstrated ability to work in a cross functional manner
- Effective oral and written communication skills with both individuals and groups. Good command of English language required.
- Aptitude for training both in-house and site personnel
- Effective interpersonal and organizational skills
- Must possess a valid drivers license where applicable.
**To become part of our team, you should**:

- RN/BSN, BS/MS or BA with 3-5 years related clinical research experience preferred or two-year
- Associates degree plus 4-5 years experience in clinical monitoring. Alternatively, a high school diploma or equivalent and 7 or more years of related experience in a scientific or healthcare field may be considered (in lieu of an academic degree) OR equivalent combination of education, training and experience
- At least 3 years clinical monitoring research experience, encompassing all the activities of a Clinical Research Associate (all types of monitoring visits) and some prior clinical lead experience

Whatever your career goals, we are here to ensure you get there!
**We invite you to join IQVIA.

Computer Research Scientist vacancy in Khamis Mushayt Saudi Arabia

Senior Computer Research Scientist

We are seeking a highly skilled and experienced Senior Computer Research Scientist to join our dynamic team in Khamis Mushayt, Saudi Arabia. In this role, you will be responsible for conducting cutting-edge research in the field of computer science and technology. Your primary focus will be on developing and implementing innovative solutions to complex problems, as well as staying up-to-date with the latest advancements in the field.

Key Responsibilities:
- Conduct in-depth research and analysis to identify new areas of potential research
- Develop and implement novel algorithms, models, and tools to tackle complex computer science problems
- Collaborate with cross-functional teams to design, develop, and test software prototypes
- Stay current with emerging technologies and industry trends
- Publish research papers in top-tier conferences and journals
- Mentor junior team members and provide guidance on their research projects

Requirements:
- PhD in Computer Science or a related field
- Minimum of 5 years of experience in computer science research or a related role
- Strong background in algorithms, data structures, machine learning, and/or artificial intelligence
- Proficient in programming languages such as Python, Java, or C++
- Excellent problem-solving skills and ability to think creatively
- Excellent written and verbal communication skills
- Ability to work independently as well as within a team

Salary: $1100 per month.
This is a full-time position without accommodation. Applicants from all nationalities are welcome to apply. We are committed to creating an inclusive workplace that values diversity. Join our team of passionate researchers today!

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MEAT SLAUGHTERHOUSE WORKER | PACKERS, SORTERS | UKRAINE | without work experience

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Computer Research Scientist vacancy in Khamis Mushayt Saudi Arabia

Entry-Level Contract Computer Research Scientist

We are hiring a motivated and detail-oriented Computer Research Scientist to join our team on a contract basis. In this role, you will conduct research and experiments to develop new computer technologies and applications. You will also analyze data and present findings to the team. The ideal candidate should have a strong understanding of computer science principles and programming languages, as well as excellent problem-solving skills. This position is open to English-speaking individuals from Pakistan with no prior experience required. If you are passionate about computer research and looking for an opportunity to gain hands-on experience, we encourage you to apply.

Salary: $1500/month

Location: Khamis Mushayt, Saudi Arabia (open to Pakistani candidates)

Requirements:
- Bachelor's degree in Computer Science or related field
- Proficiency in programming languages such as Java, C++, Python
- Strong analytical and problem-solving skills
- Excellent communication skills in English
- Ability to work independently and within a team
- Attention to detail and ability to meet deadlines

Responsibilities:
- Conduct research and experiments to develop new computer technologies and applications
- Analyze data and present findings to the team
- Collaborate with cross-functional teams on projects
- Stay updated on industry trends and advancements in technology
- Assist in writing reports, articles, or publications based on research findings

We offer a competitive salary package and a supportive work environment for individuals looking to kickstart their career in computer research. This is an entry-level position with potential for growth within the company. If you are passionate about technology and eager to learn, we would love to hear from you!

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MEAT SLAUGHTERHOUSE WORKER | PACKERS, SORTERS | UKRAINE | without work experience

1200 $

17-06-2025

We need workers in our home and office, kindly text me if you’re interested to joining

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