27 Healthcare Research jobs in Saudi Arabia

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

Experienced Clinical • Riyadh, Saudi Arabia

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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 R

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 R

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

Computer Research Scientist vacancy in Khamis Mushayt Saudi Arabia

Computer Research Scientist - Contract

We are searching for a highly skilled and motivated Computer Research Scientist to join our team on a contract basis. As a Computer Research Scientist, you will be responsible for conducting research, developing new technologies and solving complex problems in the field of computer science.

Responsibilities:
- Conduct research and experiments to develop new computer technologies
- Analyze data and develop algorithms to solve complex problems
- Collaborate with other scientists and engineers to design and implement new systems
- Develop software prototypes to test new ideas and concepts
- Stay updated with the latest advancements in computer science and technology
- Write technical reports and present findings to stakeholders

Requirements:
- Bachelor's or Master's degree in Computer Science or related field
- Proficient in programming languages such as Java, C++, Python, etc.
- Strong analytical skills and ability to think critically
- Knowledge of data mining, machine learning, and artificial intelligence techniques
- Experience with biometric passport systems is a plus
- Excellent communication skills in English (both written and verbal)
- Egyptian nationality preferred, but not required
- Available for contract work without any prior experience

Salary:
We offer a competitive salary of 1700$ per month for this contract position. Our company is committed to providing equal employment opportunities to all individuals regardless of race, color, religion, gender, national origin, age, disability or any other legally protected status.

Location:
This position is based in Khamis Mushayt City in Saudi Arabia. However, due to the current circumstances surrounding COVID-19, we are open to remote work arrangements.

We are an equal opportunity employer seeking diversity in our workforce. We also encourage women to apply for this position as we strongly believe in promoting gender equality in STEM fields. If you are a passionate Computer Research Scientist looking for an exciting opportunity to contribute your skills and knowledge on a contract basis, we would love to hear from you!

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

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Computer Research Scientist vacancy in Khamis Mushayt Saudi Arabia

Computer Research Scientist


We are currently seeking a highly skilled and motivated Computer Research Scientist to join our team in Khamis Mushayt, Saudi Arabia. As a leading research institution, we are looking for a candidate who is passionate about computer science and has a strong desire to make groundbreaking contributions in their field.

Responsibilities:
- Conduct advanced research in the field of computer science, with a focus on areas such as artificial intelligence, machine learning, data mining, or human-computer interaction.
- Develop innovative algorithms and techniques to solve complex problems.
- Design and implement experiments to test hypotheses and validate findings.
- Collaborate with other researchers and experts in related fields to explore new possibilities for research.
- Publish research papers in reputable journals and present findings at conferences.
- Stay up-to-date with latest developments and advancements in the field of computer science.

Requirements:
- A Bachelor's degree in Computer Science or a related field. A Master's or PhD degree is preferred.
- At least 3 years of experience working as a Computer Research Scientist or in a similar role.
- Strong background in one or more of the following areas: artificial intelligence, machine learning, data mining, or human-computer interaction.
- Proficient in programming languages such as Python, Java, or C++.
- Experience with statistical analysis software (e.g. R) is a plus.
- Excellent problem-solving skills and ability to think critically.
- Strong communication skills with the ability to present complex information in a clear and concise manner.

This is an urgent position and we are looking for someone who can join our team immediately. We welcome candidates from all nationalities but proficiency in English is required.

If you have a passion for pushing the boundaries of computer science and want to be part of an innovative research team, then we encourage you to apply for this position. We offer competitive salaries and benefits package along with opportunities for professional growth and development.

Note: This job description is written in simple English suitable for beginners or non-native speakers. We welcome candidates from all backgrounds and nationalities to apply for this position.

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

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