18 Medical Research jobs in Saudi Arabia

Medical Research Mentor – Support Medical Trainees in Publishing

About ResPar

ResPar is a pioneering online m
edical
research platform that connects healthcare professionals, trainees, and researchers to structured research programs. We aim to enhance research quality and capacity in the region, and we are currently
expanding our network
of mentors.

Role Overview

We are seeking motivated Research Mentors to guide healthcare trainees (medical students, residents, fellows) in completing structured research projects. Mentors will play a key role in shaping the next generation of clinician-researchers while strengthening their own academic profile.

Responsibilities

• Provide mentorship to trainees on

research design, methodology, and publication process.
- Support structured projects (cross-sectional studies, cohort studies, case control studies, and systematic reviews & meta-analysis).
- Review progress, give constructive feedback, and ensure quality of outputs for mentees under your research project mentorship program.
- The final deliverable is expected to be a high-quality research paper suitable for submission to Q1 journals indexed in WoS and Scopus.
- Participate in CPD-accredited training activities under ResPar.

Qualifications

• Medical degree (MD/MBBS) or relevant PhD/Master's in health sciences.
• Prior research experience with at least 6 peer-reviewed publications.
• Strong interest in medical education, mentorship, and research development.
• Previous supervisory or teaching experience (preferred).

What We Offer

• Per-project compensation {7,225 SAR} (specifics to be discussed during the interview)
• Opportunity to be part of an innovative research hub.
• Enhance your academic portfolio and mentorship experience.
• Flexible online engagement.
• Recognition as faculty/mentor in CPD-accredited programs (Bonus).

Apply now by sharing your CV and publication record with us @

or send to WhatsApp

Location

Riyadh, Saudi Arabia

Experience

Job Type

Recruitment

Job Description

Position: Research Scientist Level.

Job requirements: 2 to 10 years of relevant experience after PhD.

Principal Duties:

• Manages and leads the development and administration of basic Medical Research and Human Clinical Trials Research Project; Conduct research and clinical investigations and execute planned experiments.

• Makes independent decisions on routine issues and recommend scientific approaches and solutions; Assist in the periodic assessment of ongoing laboratory research studies.

• Assists in seeking a progressive growth of investigative work by submitting proposals for extramural funding of stimulating investigative studies by other medical and research staff members, and by appropriate promotional efforts of the academic programs.

• Evaluates scientific, medical diagnostics, pathologists' research applications received from members of the KAIMRC staff and for improving the quality of research proposals prior to submission to the research council for review. · Safeguards the safety guidelines when dealing with laboratory materials.

• Trains junior researchers, technologists and other staff on new experiments, platforms, equipment and technologies

• Promotes teamwork, communications and sharing of information between projects in the domain of expertise;

• Participates in long-term planning of research activities or in the field; assist in the development of the Monthly, Quarterly, and Annual Research Center reports.

• Maintains the Research Laboratories in the Research Center based on higher specialty.

• Performs other job related duties as required.

Required Specialties:

• Cancer vaccines and Cancer Immunotherapy: Candidates required with PhD or equivalent with scientific background in cancer research, Experimental immunology (flow cytometry, immune assays, cell culture, scRNA), T cell immunology (human or mouse models), CRISPR gene-engineering of immune cells, single cell analyses, T cell exhaustion, and T cell receptor engineering, cancer genetics.

• Gene therapy: Candidates required with PhD. or equivalent with scientific background in genetics, gene therapy, cell transduction, cloning, mRNA technology platform, delivery vehicles (viral vectors, LNPs) CRISPR technology, molecular biology, single-cell analytics and bioinformatics.

• Cellular Therapy: Candidates required with PhD. or PhD/MD or equivalent with scientific background in cell transduction, viral vector development, CAR-T Cell therapy approaches, molecular and cellular biology, GMP processes.

• Infectious Diseases: Candidates required with PhD. or equivalent with scientific background in virology, including molecular virology, vaccine development, BSL3 experience and bacteriology including antimicrobial resistance (AMR), bacterial genomics and bioinformatics

• Proteomics: Candidates required with PhD. or equivalent with scientific background in Quantitative proteomics, system biology, mass spectrometry, molecular biology or chemistry.

- Bioequivalence and Pharmaceutical Products Analysis: Candidates required with MSc or PhD. or equivalent with scientific background in Pharmaceutical product analysis/ quality control/ methods of analysis development, Pharmacokinetics- Pharmacodynamics (PK-PD), Bioequivalence studies, chemistry, mass spectrometry.

• Biomedical Engineering: Candidates required with PhD. or equivalent with scientific background in medical devices Prototyping, medical/diagnostic Product development,, Medical and diagnostic devices engineering.

• Nanomedicine: Candidates required with PhD. or equivalent with scientific background in Nanoparticles synthesis and characterization, Molecular sensors for diagnostics, drug delivery and chemistry.

• Bioinformatics, computational biology and Data Science: Candidates required with PhD. or equivalent with scientific background in bioinformatics, data science, drug discovery, whole genome sequencing, machine learning and artificial intelligence.

• Biostatistics: Candidates required with PhD. or equivalent with scientific background in biostatistics, Clinical Trials, Survival Analysis, Statistical Sampling, Statistical Genetics, and experimental Design.

• Population health: Candidates required with PhD. or equivalent with scientific background in popRegistry development, surveillance based research, epidemiology , cancer population health.

• Bioethics: Candidates with PhD. with strong interest and experience in bioethics and prior experience contributing to or managing institutional review boards, including strong analytical research capabilities and ability to prepare research and ethics review reports.

• Clinical Trials: Candidates with PhD/MD with prior experience conducting clinical trials and managing multi-site clinical trials at the international level. Very good understanding and ability to prepare and review clinical trials study plans, monitoring and submission to regulatory agencies.

Physical Science and Engineering Division

Organisation/Company KAUST Department Physical Science and Engineering Division Research Field Geosciences » Other Researcher Profile First Stage Researcher (R1) Recognised Researcher (R2) Established Researcher (R3) Positions Postdoc Positions Country Saudi Arabia Application Deadline 31 May 2026 - 23:59 (Asia/Riyadh) Type of Contract Temporary Job Status Full-time Hours Per Week 40 Offer Starting Date 1 Jun 2025 Is the job funded through the EU Research Framework Programme? Not funded by a EU programme Is the Job related to staff position within a Research Infrastructure? No

Professor Max Frenzel is currently recruiting for a 2-year Post-doc / Research Scientist position (extendable) to join the new Mineral Exploration and Exploitation Group at KAUST. The focus of the position will be on the development and implementation of new workflows for the mineralogical and geochemical characterization of ore materials, using combined µXRF-mapping, SEM-based automated mineralogy, and laser ablation ICP-MS, potentially complemented by powder X-ray diffraction. These workflows will then be applied to selected Saudi Arabian ore deposits to understand their genesis and exploration potential. In addition, the generated data can be used to optimize mineral extraction processes from existing mines within a geometallurgical framework.

The position will mostly focus on the development of measurement protocols and data integration methods for the different data types. In terms of applications, the candidate will be free to choose their own case study(s). Additionally, close collaboration with other group members is expected for the application of the developed workflows.

Saudi Arabia is a fast-developing country offering unparalleled opportunities in mineral resources and other geoscience-related fields. In particular, the recent opening of Saudi Arabia for international exploration companies has led to a substantial increase of activity in the mineral exploration sector. Given the great geological potential of Saudi Arabia for different types of mineral deposits, it is probably the country with the most exciting mineral exploration opportunities right now.

• Detailed experience in the use of at least one of the following analytical techniques for material characterization: X-ray spectroscopy, scanning electron microscopy, and/or laser-ablation ICP-MS is expected
• Willingness to master the other techniques required for the position.
• Excellent oral and written communication skills in English, as evidenced by a strong publication and conference presentation record.
• Experience in coding, particularly in python or R for data science and machine learning applications, are desirable.
• Willingness to participate in field work and sample collection is also desirable.
• A completed PhD is sufficient for appointment as a postdoctoral researcher. For appointment as a research scientist, additional research experience of at least 2 years is required in the relevant areas highlighted above.

• English (C1 / IELTS 7.0 equivalent or better)

Research Field GeosciencesChemistryEngineering » Materials engineering Years of Research Experience None

The position will include a competitive salary based on the candidate’s qualifications and experience; benefits include medical and dental insurance, free housing on the KAUST campus, an annual travel allowance, 30 paid vacation days, and other generous benefits. KAUST is a vibrant and international community, with many opportunities for social, sporting, and learning activities outside of work.

The successful applicant will be associated with the new Mineral Exploration and Exploitation Group at KAUST. The group will commence work in August 2025. Its main aim is to contribute to the development of mineral resources in Saudi Arabia by developing innovative approaches to mineral exploration, mining, and mineral processing. The working group will initially consist of 1 PhD student and 2 MSc students, but is projected to grow to 2 postdocs (incl. this positions), 3 PhD students, and a variable number of MSc students. In addition, KAUST provides a highly collaborative research environment, and active engagement of the holder of the position in collaborative activities within and outside of the research group will be strongly encouraged and supported.

Eligibility criteria

Applicants must hold a PhD degree in a relevant discipline, as listed above, and must demonstrate fluency in English in writing, speaking and listening at the indicated level.

Selection process

Received applications will be reviewed and suitable candidates will be interviewed on a rolling basis, starting from June 1, 2025.

Physical Science and Engineering Division

Organisation/Company KAUST Department Physical Science and Engineering Division Research Field Geosciences » Geology Geosciences » Other Mathematics » Statistics Mathematics » Other Researcher Profile First Stage Researcher (R1) Recognised Researcher (R2) Established Researcher (R3) Positions Postdoc Positions Country Saudi Arabia Application Deadline 31 May 2026 - 23:59 (Asia/Riyadh) Type of Contract Temporary Job Status Full-time Hours Per Week 40 Offer Starting Date 1 Jun 2025 Is the job funded through the EU Research Framework Programme? Not funded by a EU programme Is the Job related to staff position within a Research Infrastructure? No

Professor Max Frenzel is currently recruiting for a 2-year Post-doc position (extendable) to join the new Mineral Exploration and Exploitation Group at KAUST. The focus of the position will be on the development of new methods integrating a variety of data types (remote sensing, geology, geophysics, geochemistry) for geological modelling and advanced exploration targeting of mineral deposits. These workflows will then be applied in relevant Saudi Arabian contexts to help discover new ore deposits.

The position will combine techniques from geological modelling, geostatistics, machine learning, and potentially geophysics (inversion) to develop new exploration targeting methods. These will be designed to make the most of the excellent outcrop conditions in Saudi Arabia, which means that a particular focus will be placed on the use of remote sensing data. Other relevant data types are geological maps, geophysical surveys (gravity, electromagnetic, seismic), and soil or stream sediment geochemistry. In terms of the application to specific regions in Saudi Arabia, the candidate will be free to choose their own case study(s). The willingness to collaborate closely with local exploration companies is expected.

Saudi Arabia is a fast-developing country offering unparalleled opportunities in mineral resources and other geoscience-related fields. In particular, the recent opening of Saudi Arabia for international exploration companies has led to a substantial increase of activity in the mineral exploration sector. Given the great geological potential of Saudi Arabia for different types of mineral deposits, it is probably the country with the most exciting mineral exploration opportunities right now.

• Excellent coding skills in python, R, or another relevant language are expected, as demonstrated by previously completed projects.
• Strong candidates will also have a firm background in geostatistics, geospatial modelling, and/or data science.
• Excellent oral and written communication skills in English are required, as evidenced by a strong publication and conference presentation record.
• In addition, candidates should hold a driver’s licence or be willing to acquire one, and should be willing to undertake fieldwork.
• Experience in the mineral resource sector is desirable but not essential.
• Experience in conducting UAV surveys is desirable but not essential.
• A completed PhD is sufficient for appointment as a postdoctoral researcher. For appointment as a research scientist, additional research experience of at least 2 years is required in the relevant areas highlighted above.

English (C1 / IELTS 7.0 equivalent or better)

Level Good

Research Field Physics » OtherGeosciencesEngineering » Geological engineering Years of Research Experience None

The position will include a competitive salary based on the candidate’s qualifications and experience; benefits include medical and dental insurance, free housing on the KAUST campus, an annual travel allowance, 30 paid vacation days, and other generous benefits. KAUST is a vibrant and international community, with many opportunities for social, sporting, and learning activities outside of work.

The successful applicant will be associated with the new Mineral Exploration and Exploitation Group at KAUST. The group will commence work in August 2025. Its main aim is to contribute to the development of mineral resources in Saudi Arabia by developing innovative approaches to mineral exploration, mining, and mineral processing. The working group will initially consist of 1 PhD student and 2 MSc students, but is projected to grow to 2 postdocs (incl. this positions), 3 PhD students, and a variable number of MSc students. In addition, KAUST provides a highly collaborative research environment, and active engagement of the holder of the position in collaborative activities within and outside of the research group will be strongly encouraged and supported.

Eligibility criteria

Applicants must hold a PhD degree in a relevant discipline, as listed above, and must demonstrate fluency in English in writing, speaking and listening at the indicated level

Selection process

Received applications will be reviewed and suitable candidates interviewed on a rolling basis, starting from June 1, 2025.

Job Purpose / Summary
Responsible for staffing and managing Employee, Consultant or Freelance Clinical Research Associates (CRAs), In-House Clinical Research Associates (, Clinical Project Assistants (CPAs) and Clinical Projects Coordinators (CPCs) and ensuring adherence to and implementation of CTI policies. Manage quality and consistency of CRA services across multiple projects according to all applicable regulatory guidelines, Good Clinical Practices (GCPs) and Standard Operating Procedures (SOPs).

Essential Functions

• Responsible for the ongoing job specific training and mentoring of the subordinate CRAs and CPAs/CPCs s in accordance with Department goals and mission.  Supervision of the work of subordinate CRAs and CPAs/CPCs.
• First line of communication and escalation for the subordinate CRAs and CPAs/CPCs, including for HR and administrative issues.
• Issue, Task and Time management of the subordinate CRAs and CPAs/CPCs.
• Assuring compliance of subordinate CRAs and CPAs/CPCs to the applicable procedures, guidelines, timelines, and deliverables.
• Regular assessments and appraisals of CRAs and CPAs/CPCs and their level of competence.
• Quality Control - performs co-monitoring visits and reviews visit reports for the subordinate CRAs when needed.
• Regular reporting to Director CLO Dept. and participation in meetings with other CRMs, PMs.  Participate in the process of development and update of department-specific company SOPs and Wis when required
• Execute any activities in compliance with applicable SOPs, instructions and principles.
• Provide enough/trained resources for all projects to ensure smooth conduction of study specific activities.
• Collaborate with Director of clinical operations , on planning, assigning, and directing billable work assignments to CRAs, to ensure projects are properly resourced and study timelines are met.
• Assist in collecting preliminary and follow-up information from clients, with the purpose of identifying and evaluating project feasibility pertaining to clinical monitoring.
• Assist with defining operational Key Performance Indicators and departmental goals.
• Manage recruitment process for CRAs (and Consultant/Freelance CRAs as applicable), including review of CVs and conducting interviews collaboratively with Human Resources and others.
• Collaborate with other functional areas within CTI to ensure CRA (and Consultant/Freelance CRA as applicable) on-boarding, off-boarding, and project handovers are effective and timely

What You'll Bring:

• 2-3 years clinical research monitoring experience
• Practical experience in conducting clinical studies with pharmaceutical company or Contract Research Organization (CRO)
• Bachelor's degree in allied health fields such as nursing, pharmacy, or health science or equivalent experience as determined by CTI Management and Human Resources

About CTI
CTI Clinical Trial and Consulting Services is a global, privately held, full-service clinical contract research organization (CRO) focused on the advancement of treatments for chronically and critically ill patient populations. We assist clinical research throughout the lifecycle of development, from drug concept to commercialization. CTI is headquartered in the Greater Cincinnati, OH region with global operations in collaboration with pharmaceutical, biotechnology, and medical device firms. For more information, visit

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

• Advance Your Career - We support career progression through a structured mentoring program and leadership courses that provide the support needed to grow. We also value ongoing education and training through a dedicated training department.
• Join an Award-Winning and Valued Team - We have an award-winning unparalleled culture that can be felt by our employees across 60 countries. We support a work-life balance and the importance of time with family by offering hybrid work from home opportunities. We also encourage care for the world around us through our unique CTI Cares program.
• Make a Lasting Impact - We focus on moving medicine forward by working on treatments for chronically and critically-ill patients, who depend on us to bring life-changing therapies to market.

Important Note
In light of recent increase in hiring scams, if you're selected to move onto the next phase of our hiring process, a member of our team will reach out to you directly from email address to guide you through our interview process. Please ensure you are applying for jobs directly on our website
)
or from our verified LinkedIn page.

Please Note

• We will never communicate with you via Microsoft Teams or text message
• We will never ask for your bank account information at any point during the recruitment process

Company Description

ClinLia is a Saudi Clinical Research Organization (CRO) with extensive experience in clinical research support and management services. We operate across a broad range of therapeutic areas to align with the new vision of Saudi Arabia 2030. Our goal is to advance clinical research and innovations to position the Kingdom on the clinical trials map.

Role Description

This is a full-time, on-site role located in Riyadh for a Clinical Research Coordinator/Laboratory Qualified. The Coordinator will be responsible for overseeing day-to-day clinical research activities, obtaining informed consent from participants, ensuring adherence to protocols, and managing clinical trials. Additional duties include handling laboratory tasks, conducting research, and ensuring compliance with regulatory requirements.

Qualifications

• Experience with Informed Consent and Protocol adherence
• Background in Research and Clinical Research Experience
• Experience managing Clinical Trials
• Excellent organizational and communication skills
• Ability to work on-site in Riyadh
• Bachelor's degree in a related field (e.g., life sciences, healthcare)
• Previous experience in a laboratory setting is a plus

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
• Fluent in English

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.
• Our culture is unparalleled – We've received multiple awards recognizing CTI as one of the best places to work in the greater Cincinnati area, as well as one of the top CROs in the industry
• 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

Are you interested? Then we look forward to your electronic application, with a tabular CV in English.

CTI Clinical Trial and Consulting Services

Filipa Magalhães

Position Summary:

We are seeking a highly skilled and motivated PhD-level R&D Scientist with 3–4 years of experience in drilling fluid systems and simulation modeling. The ideal candidate will lead and contribute to the development and optimization of advanced drilling fluid technologies and digital simulation tools to enhance wellbore stability, efficiency, and sustainability in drilling operations.

This is a strategic role for someone who combines deep technical knowledge with hands-on experience in lab research, fluid rheology, and numerical modeling.

Key Responsibilities:

• Lead and conduct R&D projects focused on designing, testing, and improving drilling fluid systems (water-based, oil-based, synthetic-based, or polymer-based).
• Develop and implement simulation models (e.g., hydraulics, thermal modeling, cuttings transport, fluid loss) to predict drilling fluid performance in various well conditions.
• Utilize numerical tools (e.g., ANSYS, COMSOL, CFD, or custom simulators) to optimize formulations and drilling parameters.
• Conduct laboratory experiments to assess rheology, stability, filtration, and other key drilling fluid properties under HPHT conditions.
• Analyze experimental and field data to correlate simulation models with real-world performance.
• Collaborate with field engineers, product development teams, and clients to troubleshoot field challenges and deliver customized fluid solutions.
• Write technical reports, research papers, and contribute to patent filings and conference presentations.
• Stay updated on emerging technologies, materials, and digital innovations in drilling and well construction.

Required Qualifications:

• PhD in Chemistry , Petroleum Engineering, Chemical Engineering, or a related field with a specialization in drilling fluids .
• 3–4 years of industry or academic R&D experience focused on drilling fluid systems and simulation.
• Strong knowledge of fluid rheology, wellbore hydraulics, HPHT testing, and formation interactions.
• Strong problem-solving abilities and capability to design and conduct structured research programs.
• Excellent written and verbal communication skills, including the ability to present technical findings to both technical and non-technical audiences

JOB PURPOSE / SUMMARY

Responsible for project activities associated with monitoring functions of phase I through phase IV clinical research studies and Real World Evidence (RWE) studies, while developing an understanding of drug development process, International Council for Harmonisation (ICH) / Good Clinical Practice (GCP) and relevant regulations. Performs management of study site activities in adherence to all applicable regulatory guidelines and Standard Operating Procedures (SOPs).

ESSENTIAL FUNCTIONS

• Serve as main CTI contact for assigned study sites

• Conduct site visits (pre-study (PSV), site initiation (SIV), interim monitoring (IMV), and close-out (COV)) and complete site visit deliverables with quality and within given timelines in Monitoring Plan while adhering to all applicable regulatory requirements, SOPs and ICH GCP

• Assist with study start-up activities, including feasibility, pre-study activities and site selection

• Collect, review and track essential/regulatory documents
• Participate in and complete all general and study specific training as required
• Participate in investigator, client and project team meetings
• Assist in developing patient enrollment strategies with Project Team and study sites
• Ensure proper storage, dispensation and accountability of all Investigational Product (IP) and trial-related materials
• Perform site management activities and provide ongoing updates of site status to Clinical Project Manager
• Conduct remote monitoring and complete all the related activities in accordance with study specific Monitoring Plan
• Utilize systems and reports to track subject status, subject case report form (CRF) retrieval / source document review (SDV), regulatory documents, and IP
• Assist with project-specific activities as member of Project Team
• May support in development of CRFs and other study related documents (subject worksheets, Monitoring Plan, etc.
• May support in the translation, customization, and review of Patient Information sheet and Informed Consent, protocol synopsis and other study applicable documents as per required procedures
• Where applicable, provide support to Regulatory Affairs Study Start-up Team in the preparation or revision of documentation for submission to Ethics Committee(s), Institutions Ethics Committees, Regulatory Authorities, Competent Authorities or Institutions Administration Boards, and follow-up the evaluation process until approval is available.
• Provide regular updates to Sponsor/ Client
• Where applicable, support in contract negotiation with study sites, Investigator payments and tracking of site payments
• Manage ISF and TMF for all assigned study sites in accordance with SOPs or study-specific Monitoring Plans
• Identify site issues and implement corrective actions or escalate as appropriate
• Liaise with Clinical Data Management for data cleaning activities

What You'll Bring:

• At least 2 years of clinical nursing experience, or at least 1 year of experience in related health care or clinical research work experience (ONCOLOGY) (ie, Study Coordinator), or at least 1 year experience performing relevant project support in-house functions

• Bachelor's Degree or higher in allied health field such as nursing, pharmacy, or health / natural science, or RN with Associate's Degree, or 3-year Nursing Diploma with at least 2 years clinical nursing experience, or equivalent experience as determined by CTI Management and Human Resources

About CTI

CTI Clinical Trial and Consulting Services is a global, privately held, full-service clinical contract research organization (CRO) focused on the advancement of treatments for chronically and critically ill patient populations. We assist clinical research throughout the lifecycle of development, from drug concept to commercialization. CTI is headquartered in the Greater Cincinnati, OH region with global operations in collaboration with pharmaceutical, biotechnology, and medical device firms. For more information, visit

Why CTI?

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

• Advance Your Career - We support career progression through a structured mentoring program and leadership courses that provide the support needed to grow. We also value ongoing education and training through a dedicated training department.
• Join an Award-Winning and Valued Team - We have an award-winning unparalleled culture that can be felt by our employees across 60 countries. We support a work-life balance and the importance of time with family by offering hybrid work from home opportunities. We also encourage care for the world around us through our unique CTI Cares program.
• Make a Lasting Impact - We focus on moving medicine forward by working on treatments for chronically and critically-ill patients, who depend on us to bring life-changing therapies to market.

Important Note

In light of recent increase in hiring scams, if you're selected to move onto the next phase of our hiring process, a member of our team will reach out to you directly from  email address to guide you through our interview process. Please ensure you are applying for jobs directly on our website
)
or from our verified LinkedIn page.

Please Note

• • We will never communicate with you via Microsoft Teams or text message
• We will never ask for your bank account information at any point during the recruitment process