18 Study Coordinator jobs in Saudi Arabia

Join to apply for the FREELANCERS ONLY: Audio Data Collection – German & Arabic Speakers (Short-Term Project) role at DATAmundi

Join to apply for the FREELANCERS ONLY: Audio Data Collection – German & Arabic Speakers (Short-Term Project) role at DATAmundi

Hello, dear partner!

We’re looking for German and Arabic speakers to join a short-term audio data collection project focused on improving speech recognition technologies.

This is a remote opportunity that requires no previous experience and no educational background — just your voice and attention to detail!

What’s the Project About?

We're collecting and reviewing 2,500 unique German voice recordings as part of a global speech dataset. The project will run for 6 weeks, and we are looking to onboard large numbers of contributors and reviewers in both German and Arabic.

️ Who Can Apply?

Contributors (Recording Voice Samples)

• Proficient in spoken German or Arabic (non-native speakers welcome)
• Average task time: 2 minutes per recording
• No special equipment or setup needed
  
  

• Native speakers of German or Arabic
• Average task time: 4 minutes per item
• Strong attention to detail is a plus
  
  

• Project Duration: 6 weeks
• Tasks are short and can be completed flexibly
• Ideal for students, freelancers, or anyone looking to contribute part-time
  
  

• 500 contributors per language
  
  

• No prior experience required
• No educational background needed
• Participation from a diverse range of regions is encouraged. The location set in this post is for reference only and not selective.
  
  

• Seniority level Internship

• Employment type Part-time

• Job function Other
• Industries Translation and Localization

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Below you will find the details for the position including any supplementary documentation and questions you should review before applying for the opening. To apply for the position, please click the Apply for this Job link/button.

If you would like tobookmark this position for later review, click on the Bookmark link. To email this position to a friend, click on the Email to a Friend link. If you would like to print a copy of this position for your records, click on the Print Preview link.

1. Applications are invited for faculty positions as soon as possible at King Fahd University of Petroleum & Minerals, Dhahran, Saudi Arabia.

2. Applicants must be fluent in English as it is the medium of instruction in the University.

3. A good track record of research and of handling projects independently.

Job Reference Number

Job Reference Number F208

Job Title

Job Title Research Scientist - Applied Research Center for Environment & Marine Studies - RI

Location

Type

Type Full Time

Job Description

The Center for Environment & Marine Studies at KFUPM is seeking qualified researchers to fill a research scientist position. The potential candidate must hold a Ph.D. degree in Chemistry with experience in Analytical and Environmental Chemistry. Besides, they must utilize that experiment in the environmental monitoring and in the determination of hazardous contaminants such as TPH (Total Petroleum Hydrocarbon), PAH (Polycyclic Aromatic Hydrocarbon), polychlorinated, and BTEX (benzene, ethylbenzene, and toluene) in water, sediment and biota samples using different analytical instruments such as GC-MS, HPLC and LC-MS.

Job Responsibility

· Perform samples analysis for quantification of different environmental pollutants using the most common analytical techniques GC- FID , GC-MS, HPLC and LC-MS.

· Train joiner chemists on the advanced analytical techniques.

· Conduct basic and applied research related to water treatment, analytical method development and environmental monitoring.

· Publish findings in reputable peer reviewed journals.
· Write research proposals.

Competitive salary based on qualifications and experience. The appointment includes the following benefits according to the university policy.
1. Tax free salary.
2. Free furnished air-conditioned on-campus housing unit with free essential utilities and maintenance.
3. Air ticket/s to Dhahran on appointment.
4. Annual repatriation air ticket/s for family members up to four persons.
5. 30 days of paid vacation.
6. Assistance with local tuition fees for school-aged dependent children.
7. Transportation allowance
8. Medical insurance
9. End-of-service gratuity after two (2) years of continuous service.
The KFUPM campus has a range of facilities including a medical and dental clinic, health club with swimming pool, an extensive library, computing, research

Qualifications

· PhD degree in Analytical Chemistry.

· Has an experience in a research centers similar to the Center for Environment & Marine Studies whose working in the environmental monitoring and in the determination of hazardous contaminants such as TPH (Total Petroleum Hydrocarbon), PAH (Polycyclic Aromatic Hydrocarbon), polychlorinated, and BTEX (benzene, ethylbenzene, and toluene) in water, sediment and biota samples.

· Experience in Analytical instruments such as GC-MS, HPLC and LC-MS.

· Published a good number of articles in reputable journals

· Ability to work with interdisciplinary research groups.

Special Instructions to Applicants

1. Applications are invited for faculty positions as soon as possible at King Fahd University of Petroleum & Minerals, Dhahran, Saudi Arabia.

2. Applicants must be fluent in English as it is the medium of instruction in the University.

3. A good track record of research and of handling projects independently.

Contact Information

Director of Talent Acquisition Department
King Fahd University of Petroleum & Minerals
KFUPM Box 5005, Dhahran 31261
Saudi Arabia
Email:

Open Date

Close Date

Open Until Filled Yes

Required fields are indicated with an asterisk (*).

• * Highest Education Level you have earned ?
  • Bachelor
  • Masters
  • PhD or above
• * How did you hear about this employment opportunity?

  (Open Ended Question)

Documents Needed to Apply

Required Documents

• Resume
• Cover Letter/Letter of Application
• All Official Transcripts (BS, MS, Ph.D.) combined in one file
• All Degrees and Certifications (BS, MS, Ph.D.) combined in one file
• Abstract of the Dissertation
• Scanned copy of Passport
• Applicant Photo
• Teaching Statement
• Research Statement
• List of Publications
Optional Documents
• Other Document
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Below you will find the details for the position including any supplementary documentation and questions you should review before applying for the opening. To apply for the position, please click the Apply for this Job link/button.

If you would like tobookmark this position for later review, click on the Bookmark link. To email this position to a friend, click on the Email to a Friend link. If you would like to print a copy of this position for your records, click on the Print Preview link.

1. Applications are invited for faculty positions as soon as possible at King Fahd University of Petroleum & Minerals, Dhahran, Saudi Arabia.

2. Applicants must be fluent in English as it is the medium of instruction in the University.

3. A good track record of research and of handling projects independently.

Job Reference Number

Job Reference Number F208

Job Title

Job Title Research Scientist - Applied Research Center for Environment & Marine Studies - RI

Location

Type

Type Full Time

Job Description

The Center for Environment & Marine Studies at KFUPM is seeking qualified researchers to fill a research scientist position. The potential candidate must hold a Ph.D. degree in Chemistry with experience in Analytical and Environmental Chemistry. Besides, they must utilize that experiment in the environmental monitoring and in the determination of hazardous contaminants such as TPH (Total Petroleum Hydrocarbon), PAH (Polycyclic Aromatic Hydrocarbon), polychlorinated, and BTEX (benzene, ethylbenzene, and toluene) in water, sediment and biota samples using different analytical instruments such as GC-MS, HPLC and LC-MS.

Job Responsibility

Perform samples analysis for quantification of different environmental pollutants using the most common analytical techniques GC- FID , GC-MS, HPLC and LC-MS.

Train joiner chemists on the advanced analytical techniques.

Conduct basic and applied research related to water treatment, analytical method development and environmental monitoring.

Publish findings in reputable peer reviewed journals.
Write research proposals.

Competitive salary based on qualifications and experience. The appointment includes the following benefits according to the university policy.
1. Tax free salary.
2. Free furnished air-conditioned on-campus housing unit with free essential utilities and maintenance.
3. Air ticket/s to Dhahran on appointment.
4. Annual repatriation air ticket/s for family members up to four persons.
5. 30 days of paid vacation.
6. Assistance with local tuition fees for school-aged dependent children.
7. Transportation allowance
8. Medical insurance
9. End-of-service gratuity after two (2) years of continuous service.
The KFUPM campus has a range of facilities including a medical and dental clinic, health club with swimming pool, an extensive library, computing, research

Qualifications

PhD degree in Analytical Chemistry.

Has an experience in a research centers similar to the Center for Environment & Marine Studies whose working in the environmental monitoring and in the determination of hazardous contaminants such as TPH (Total Petroleum Hydrocarbon), PAH (Polycyclic Aromatic Hydrocarbon), polychlorinated, and BTEX (benzene, ethylbenzene, and toluene) in water, sediment and biota samples.

Experience in Analytical instruments such as GC-MS, HPLC and LC-MS.

Published a good number of articles in reputable journals

Ability to work with interdisciplinary research groups.

Special Instructions to Applicants

1. Applications are invited for faculty positions as soon as possible at King Fahd University of Petroleum & Minerals, Dhahran, Saudi Arabia.

2. Applicants must be fluent in English as it is the medium of instruction in the University.

3. A good track record of research and of handling projects independently.

Contact Information

Director of Talent Acquisition Department
King Fahd University of Petroleum & Minerals
KFUPM Box 5005, Dhahran 31261
Saudi Arabia
Email:

Open Date

Close Date

Open Until Filled Yes

Required fields are indicated with an asterisk ( ).

• Highest Education Level you have earned ?
  • Bachelor
  • Masters
  • PhD or above
• How did you hear about this employment opportunity?

  (Open Ended Question)

Documents Needed to Apply

Required Documents

• Resume
• Cover Letter/Letter of Application
• All Official Transcripts (BS, MS, Ph.D.) combined in one file
• All Degrees and Certifications (BS, MS, Ph.D.) combined in one file
• Abstract of the Dissertation
• Scanned copy of Passport
• Applicant Photo
• Teaching Statement
• Research Statement
• List of Publications
Optional Documents
• Other Document

The Center for Environment & Marine Studies at KFUPM is seeking qualified researchers to fill a Research Scientist III position. The potential candidate must hold a Ph.D. degree.

• Field studies
• Publish findings in reputable peer-reviewed journals
• Write research proposals

• PhD degree
• Experience in research centers similar to the Center for Environment & Marine Studies

• Tax-free salary
• Free furnished air-conditioned on-campus housing unit with free essential utilities and maintenance
• Air ticket/s to Dhahran on appointment
• Annual repatriation air ticket/s for family members up to four persons
• 30 days of paid vacation
• Assistance with local tuition fees for school-aged dependent children
• Transportation allowance
• Free health care at KFUPM Clinic
• End-of-service gratuity after two (2) years of continuous service

Director of Talent Acquisition Department
King Fahd University of Petroleum & Minerals
KFUPM Box 5005, Dhahran 31261
Saudi Arabia
Email:
Telephone: +966 13 860-7854
Fax: +966 13 860-2442

Required fields are indicated with an asterisk (*).

• * Highest Education Level you have earned?
  • Bachelor
  • Masters
  • PhD or above
• * How did you hear about this employment opportunity?

  (Open Ended Question)

Required Documents

• Resume
• Cover Letter/Letter of Application
• All Official Transcripts (BS, MS, Ph.D.) combined in one file
• All Degrees and Certifications (BS, MS, Ph.D.) combined in one file
• Abstract of the Dissertation
• Scanned copy of Passport
• Applicant Photo
• Teaching Statement
• Research Statement
• List of Publications

Optional Documents

• Other Document

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

IQVIA 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

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

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

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

IQVIA 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