project manager

pmo manager

project director

senior project manager

commercial manager

clinical research manager

<div><p>Job Description</p><p></p><p>
Are you passionate about driving high‑quality clinical trials and building strong partnerships with investigators? Do you thrive in a role that combines <b>end‑to‑end study ownership, cross‑functional leadership, and strategic impact</b>?</p><p>
We are looking for a <b>Clinical Research Manager (CRM)</b> to lead the operational delivery of clinical trials at country (and potentially cluster) level, ensuring excellence in execution, compliance, and stakeholder collaboration.</p><p></p><h2 class="jobSectionHeader"><b>
Key Responsibilities</b></h2><ul><li><p>
Serve as the <b>main point of contact</b> for assigned protocols, representing country operations within global Clinical Trial Teams</p></li><li><p>
Lead <b>end‑to‑end project management</b> of clinical trials&mdash;from feasibility and site selection through execution and close‑out</p></li><li><p>
Ensure <b>compliance with ICH/GCP, local regulations, internal policies, and safety reporting requirements</b></p></li><li><p>
Drive study performance by proactively planning, tracking, and resolving risks related to timelines, quality, and recruitment</p></li><li><p>
Lead and coordinate <b>local study teams</b>, acting as protocol expert and supporting CRAs and other country roles</p></li><li><p>
Review monitoring visit reports, identify performance gaps, and escalate issues as needed</p></li><li><p>
Conduct <b>quality control visits</b> when required</p></li><li><p>
Develop and execute <b>local risk management plans</b> for assigned studies</p></li><li><p>
Ensure accurate and timely use of <b>CTMS, eTMF, and other key systems</b></p></li><li><p>
Build strong, trust‑based relationships with <b>investigators, vendors, and external partners</b></p></li><li><p>
Share best practices across studies, countries, and clusters</p></li><li><p>
Contribute to <b>local and regional clinical operations strategy</b> in collaboration with internal stakeholders</p></li></ul><h3 class="jobSectionHeader"><b>
Experience &amp; Education</b></h3><ul><li><p>
Bachelor&rsquo;s degree in Science or equivalent (advanced degree preferred)</p></li><li><p><b>
5&ndash;6 years of experience in clinical research</b></p></li><li><p>
CRA experience is an advantage</p></li></ul><h3 class="jobSectionHeader"><b>
Core Skills</b></h3><ul><li><p>
Strong <b>project and site management</b> expertise</p></li><li><p>
Solid understanding of <b>clinical trial planning, execution, and performance metrics</b></p></li><li><p>
Excellent knowledge of the <b>local regulatory environment</b></p></li><li><p>
Ability to manage multiple studies and priorities simultaneously</p></li><li><p>
Fluent in <b>English and local language (Arabic)</b>, with strong written and verbal communication skills</p></li></ul><h3 class="jobSectionHeader"><b>
Leadership &amp; Behaviors</b></h3><ul><li><p>
Proven ability to <b>lead without direct authority</b> and influence cross‑functional teams</p></li><li><p>
Strong problem‑solving and risk‑mitigation mindset</p></li><li><p>
Skilled in navigating complex situations such as recruitment challenges, compliance issues, and resource constraints</p></li><li><p>
Collaborative, culturally aware, and effective in <b>remote/virtual environments</b></p></li><li><p>
Professional, diplomatic, and confident when engaging with investigators and stakeholders</p></li></ul><p></p><p><b>
Required Skills:
</b></p>Clinical Data Management, Clinical Research, Clinical Site Management, Clinical Trial Management Processes, Clinical Trials Operations, Good Clinical Practice (GCP), Planning, Project Management, Quality Management, Risk Management, Stakeholder Engagement<p></p><p><b>
Preferred Skills:
</b></p><p></p><p>Current Employees apply HERE</p><p></p><p>
Current Contingent Workers apply HERE</p><p></p><p><b>
Search Firm Representatives Please Read Carefully</b><br>
Merck &amp; Co., Inc., Rahway, NJ, USA, also known as Merck Sharp &amp; Dohme LLC, Rahway, NJ, USA, does not accept unsolicited assistance from search firms for employment opportunities. All CVs / resumes submitted by search firms to any employee at our company without a valid written search agreement in place for this position will be deemed the sole property of our company. No fee will be paid in the event a candidate is hired by our company as a result of an agency referral where no pre-existing agreement is in place. Where agency agreements are in place, introductions are position specific. Please, no phone calls or emails.</p><p></p><p><b>
Employee Status:
</b></p>Regular<p></p><p><b>
Relocation:</b></p><p></p><p><b>
VISA Sponsorship:</b></p><p></p><p><b>
Travel Requirements:</b></p><p></p><p><b>
Flexible Work Arrangements:</b></p>
Hybrid<p></p><p><b>
Shift:</b></p><p></p><p><b>
Valid Driving License:</b></p><p></p><p><b>
Hazardous Material(s):</b></p><p></p><p><b>
Job Posting End Date:</b></p>
04/27/2026<ul><li><b>A job posting is effective until 11:59:59PM on the day </b><b>BEFORE</b><b> the listed job posting end date. Please ensure you apply to a job posting no later than the day </b><b>BEFORE</b><b> the job posting end date.<br>
</b></li></ul><br>
<p><b>Requisition ID:</b>R392298</p></div>

Clinical Research Manager

Sanofi

<div><div><div><div><p><b>Job title: </b>Medical Science Liaison &ndash; Immunology (Respiratory &amp; GI)</p><ul><li><b>
Location:</b> <i>Riyadh, Kingdom of Saudi Arabia</i></li></ul><p></p><p><b>
About the job</b></p><p>
As a <b>Medical Science Liaison &ndash; Immunology (Respiratory &amp; GI)</b> within our Specialty Care team, you'll serve as the vital bridge between cutting-edge science and clinical practice. You'll build trusted relationships with key scientific experts, support clinical research initiatives, and bring real-world medical insights back to our brand teams to help shape breakthrough treatments for patients with immune challenges. Ready to get started?</p><p>
Join the team transforming care for people with immune challenges, rare diseases, cancers, and neurological conditions. In Specialty Care, you'll help deliver breakthrough treatments that bring hope to patients with some of the highest unmet needs.</p><p></p><p><b>
About Sanofi</b></p><p>
We're an R&amp;D-driven, AI-powered biopharma company committed to improving people's lives and delivering compelling growth. Our deep understanding of the immune system &ndash; and innovative pipeline &ndash; enables us to invent medicines and vaccines that treat and protect millions of people around the world. Together, we chase the miracles of science to improve people's lives.</p><p></p><p><b>
Main responsibilities</b></p><ul><li>
Build and maintain balanced scientific relationships with key external experts to deepen understanding of customer research needs and opportunities in Immunology (Respiratory &amp; GI).</li><li>
Develop a clear understanding of the healthcare ecosystem through stakeholder mapping and identifying key milestones in patient journeys.</li><li>
Provide healthcare professionals and decision-makers with accurate, balanced, and timely scientific information about our Immunology portfolio.</li><li>
Collaborate closely with Medical Affairs and clinical teams to coordinate Phase IV clinical projects, facilitate investigator-sponsored study submissions, support publications, and assist in site selection.</li><li>
Act as a product expert supporting commercial teams during training sessions, particularly in handling medical objections.</li><li>
Serve as the primary source of real-world medical insights and scientific expert feedback from the field to brand teams.</li><li>
Represent Sanofi at key medical and scientific conferences by staffing medical information booths, gathering competitive intelligence, and observing sponsored speakers.</li><li>
Receive, document, and report adverse events according to company procedures and ensure risk management plan implementation and monitoring.</li></ul><p><b>
About you</b></p><ul><li><b>
Education:</b> University degree in life sciences required; MD, PhD, or PharmD strongly preferred</li><li><b>
Experience:</b> At least 2 years of experience in specialty care and/or Immunology/Gastroenterology is a plus</li><li><b>
Technical skills:</b> Strong knowledge of clinical research methodology and Good Clinical Practice (GCP)</li><li><b>
Communication skills:</b> Ability to communicate effectively at various management levels, including with scientific external experts</li><li><b>
Soft skills:</b> Self-motivated team player with business acumen, resource planning abilities, and the capacity to inspire and motivate others</li><li><b>
Languages:</b> Full professional proficiency in English and Arabic</li></ul><p><b>
Why choose us?</b></p><ul><li>
Work at the intersection of cutting-edge immunoscience and patient care, helping deliver breakthrough treatments to those with the highest unmet medical needs.</li><li>
Build meaningful relationships with leading scientific experts and key opinion leaders while contributing to clinical research that shapes the future of Immunology care.</li><li>
Develop your career in a purpose-driven environment with opportunities to grow across therapeutic areas, functions, and geographies.</li><li>
Collaborate with diverse, multidisciplinary teams across Medical Affairs, Clinical Research, and Commercial functions to drive patient impact.</li><li>
Thrive in a workplace that values scientific excellence, ethical leadership, and your personal well-being with comprehensive benefits and flexible working options.</li></ul><p><b>
Pursue</b> <i>Progress</i>. <b>Discover</b> <i>Extraordinary.</i></p><p>
Join Sanofi and step into a new era of science - where your growth can be just as transformative as the work we do. We invest in you to reach further, think faster, and do what's never-been-done-before. You'll help push boundaries, challenge convention, and build smarter solutions that reach the communities we serve. Ready to chase the miracles of science and improve people's lives? Let's Pursue <i>Progress</i> and Discover <i>Extraordinary</i> &ndash; together.</p><p>
At Sanofi, we provide equal opportunities to all regardless of race, color, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, disability, gender identity, protected veteran status or other characteristics protected by law</p></div></div></div>
null</div>

Medical Science Liaison

Novartis

<div><div><h3 class="jobSectionHeader"><b>Summary
</b></h3><div>To serve as a liaison to the medical/ scientific community and responsible for establishing, devel-oping and partnering with Health Care Providers/ Professionals (HCPs), e.g. external Medical Ex-perts, study investigators, treatment guideline experts, etc. to ensure the appropriate dissemina-tion of clinical and scientific information regarding Novartis&rsquo; compounds in a timely, ethical and stakeholder-focused manner. To implement clinical and educational strategies in collaboration with other Novartis colleagues for designated stakeholders. To pair key stakeholders&rsquo; scientific educational and research needs with available Novartis resources and provide the latest emerging data in response to specific HCP inquiries, as appropriate.<br>
<br>
#LI-Onsite</div>
</div><div><h3 class="jobSectionHeader"><b>About the Role
</b></h3><div><h3 class="jobSectionHeader"><b>Medical Expert Engagement</b></h3><ul><li>
Identify, map, and engage Medical Experts and study investigators in alignment with the Integrated Product Strategy (IPS).</li><li>
Share medical, scientific, and health outcomes evidence on Novartis compounds, therapeutic areas, and new treatment options with HCPs and key stakeholders.</li></ul><h3 class="jobSectionHeader"><b>
Scientific Information &amp; Requests</b></h3><ul><li>
Respond to unsolicited HCP requests by presenting globally approved data, including compounds in development.</li><li>
Involve HCPs in advisory boards, educational activities, and publications when relevant.</li></ul><h3 class="jobSectionHeader"><b>
Clinical Research Support</b></h3><ul><li>
Educate on Novartis clinical research programs, recommend study sites, and support trial feasibility and accrual.</li><li>
Facilitate IIT submissions and material transfer agreements for independent research.</li></ul><h3 class="jobSectionHeader"><b>
Scientific Exchange &amp; Insights</b></h3><ul><li>
Promote scientific exchange on emerging principles and trends.</li><li>
Collect and report HCP insights to inform medical strategy and IPS planning.</li></ul><h3 class="jobSectionHeader"><b>
Internal Contributions</b></h3><ul><li>
Act as a local medical resource for disease area and product training.</li><li>
Contribute to IPS and Medical Affairs strategy design and execution.</li></ul><h3 class="jobSectionHeader"><b>
Compliance &amp; Integrity</b></h3><ul><li>
Ensure adherence to all compliance processes (e.g., IIT, Medical Affairs Field Interactions).</li><li>
Foster a diverse, inclusive, and harassment-free environment.</li></ul><h3 class="jobSectionHeader"><b>
Education &amp; Communication</b></h3><ul><li>
Provide scientific and educational information to HCPs on patient-critical issues.</li><li>
Support internal capability building through training and knowledge sharing.</li></ul><p></p><p><b>
Minimum Requirements</b></p><ul><li>
A degree in PharmD, PhD, MD (Medical Doctor) is essential.</li><li>
At least 1-year experience as Medical Science Liaison, specific experience in Hematology is a plus.</li><li>
Fluent in both Arabic and English languages.</li></ul></div><p></p>
</div><div><div><p><b>Why Novartis:</b> Helping people with disease and their families takes more than innovative science. It takes a community of smart, passionate people like you. Collaborating, supporting and inspiring each other. Combining to achieve breakthroughs that change patients&rsquo; lives. Ready to create a brighter future together? https://www.novartis.com/about/strategy/people-and-culture</p><p><b>
Benefits and Rewards:</b> Learn about all the ways we&rsquo;ll help you thrive personally and professionally.<br>
Read our handbook (PDF 30 MB)</p></div></div></div>
<br><div><div>Division
<div>International
</div></div><div>Business Unit
<div>Development
</div></div><div>Location
<div>Saudi Arabia
</div></div><div>Site
<div>Riyadh
</div></div><div>Company / Legal Entity
<div>SA01 (FCRS = SA001) Novartis Saudi Arabia Ltd
</div></div><div>Alternative Location 1
<div>Jeddah, Saudi Arabia
</div></div><div>Functional Area
<div>Research &amp; Development
</div></div><div>Job Type
<div>Full time
</div></div><div>Employment Type
<div>Regular
</div></div><div>Shift Work
<div>No
</div></div><div></div><div><p>Novartis is committed to building an outstanding, inclusive work environment and diverse teams' representative of the patients and communities we serve.</p></div></div>

Senior Hematology Medical Science Liaison - Riyadh

Bdjobs.com

<div>
 <p>
  <strong>
   The Nazifa Recruitment Services
  </strong>
  is looking for
  <strong>
   Consultant/Specialist Doctor (Saudi Arabia)
  </strong>
 </p>
 <p>
  <br/>
 </p>
 <p>
  <strong>
   Job Description / Responsibility
  </strong>
 </p>
 <ul>
  <li>
   <strong>
    Clinical Care &amp; Decision-Making:
   </strong>
   They perform complex procedures, evaluate patients, interpret diagnostic tests, and develop personalized treatment plans, often using dual-process thinking to ensure accuracy.
  </li>
  <li>
   <strong>
    Specialized Expertise:
   </strong>
   Provide expert opinions on challenging cases, acting as the final authority on clinical decisions within their specialty.
  </li>
  <li>
   <strong>
    Leadership &amp; Team Management:
   </strong>
   Lead multidisciplinary teams (MDTs) to deliver comprehensive care and manage rotas.
  </li>
  <li>
   <strong>
    Supervision &amp; Mentorship:
   </strong>
   Teach and mentor junior doctors, medical students, and nursing staff.
  </li>
  <li>
   <strong>
    Clinical Governance &amp; Safety:
   </strong>
   Ensure compliance with healthcare regulations, ethical standards, and hospital protocols to maintain safety.
  </li>
  <li>
   <strong>
    Research &amp; Education:
   </strong>
   Participate in medical research, service development, and continuous professional development (CPD).
  </li>
 </ul>
 <p>
  <strong>
   Educational Requirements
  </strong>
 </p>
 <ul>
  <li>
   Bachelor of Medicine and Bachelor of Surgery(MBBS)
  </li>
  <li>
   Doctor of Medicine (MD)
  </li>
  <li>
   Master of Surgery (MS)
  </li>
  <li>
   Fellowship of the College of Physicians and Surgeons (FCPS)
  </li>
  <li>
   Diploma
  </li>
  <li>
   Accepted post graduate degree: MBBS+ MS, MD, FCPS, MPhil, MRCP, MRCS, Diploma
  </li>
  <li>
   Skills Required: Health/ Medical
  </li>
 </ul>
 <p>
  <strong>
   Experience Requirements
  </strong>
 </p>
 <ul>
  <li>
   2 to 6 year(s)
  </li>
  <li>
   The applicants should have experience in the following business area(s):
  </li>
  <li>
   Hospital
  </li>
 </ul>
 <p>
  <strong>
   Note:
  </strong>
 </p>
 <ul>
  <li>
   Need minimum 2-5 years of working experience after post graduation
  </li>
 </ul>
 <p>
  <strong>
   Salary
  </strong>
 </p>
 <ul>
  <li>
   Tk. 800000 - 1200000 (Monthly)
  </li>
 </ul>
</div>


Consultant/Specialist Doctor (Saudi Arabia)- For The Nazifa Recruitment Services- Job ID: 1475498

Rawaj - Human Capital Management

<div><p><b>Leverage your expertise and join a leading company specializing in leading Pharmaceutical and medical devices company in Saudi Arabia.</b></p><p><b>
 </b>The <b>Product &amp; Business Development Manager</b> will be responsible for identifying and developing new products, conducting market insights and analysis, and establishing strategic partnerships, while working closely with R&amp;D and Regulatory Affairs teams to ensure successful product development and market entry.</p><h3 class="jobSectionHeader"><b>
Key Accountabilities</b></h3><ul><li><p>
Conduct in-depth <b>market research and analysis</b> to identify new product opportunities and unmet clinical needs in Saudi Arabia.</p></li><li><p>
Lead <b>product development initiatives</b> in coordination with R&amp;D and Regulatory Affairs teams.</p></li><li><p>
Translate market insights into actionable product strategies and portfolio expansion plans.</p></li><li><p>
Identify, evaluate, and onboard new <b>suppliers and manufacturing partners</b> to enhance product offerings.</p></li><li><p>
Build and maintain strong relationships with suppliers, principals, and international manufacturers.</p></li><li><p>
Collaborate with internal teams (Sales, Marketing, Regulatory, Supply Chain, Finance) for successful product launches.</p></li><li><p>
Monitor <b>product and business development KPIs</b>, opportunity pipelines, and performance metrics.</p></li><li><p>
Represent the company in supplier meetings, industry events, exhibitions, and conferences.</p></li><li><p>
Leverage established relationships with <b>NUPCO</b>, government authorities, hospitals, and distributors to support tenders, product listings, and long-term contracts.</p></li></ul><p><b>
Knowledge, Skills, and Experience</b></p><ul><li><p>
Bachelor&rsquo;s degree in <b>Pharmacy, Biomedical Engineering, Business Administration</b>, or related field (<b>MBA preferred</b>).</p></li><li><p>
Minimum <b>10+ years of experience</b> in <b>product development, market insights, or business development</b> within the medical devices industry.</p></li><li><p>
Proven experience in <b>product strategy, supplier management, and R&amp;D coordination</b>.</p></li><li><p>
Strong understanding of the <b>Saudi healthcare market, medical device regulations, and procurement processes</b> including NUPCO.</p></li><li><p>
Demonstrated ability to assess market opportunities and convert insights into viable products.</p></li><li><p>
Excellent <b>analytical, strategic thinking, negotiation, and stakeholder management</b> skills.</p></li></ul></div>

Product & Business Development Manager – Pharmaceutical | Saudi Arabia

Salehiya Healthcare

<div>
 <p>
  <strong>
   About Us:
  </strong>
 </p>
 <p>
  Salehiya started commercial activities in 1964 as a specialized healthcare company. It is one of the leading Saudi Arabian companies in distributing pharmaceuticals, medical and laboratory equipment, diagnostics, medical disposables, and hospital and consumer supplies. The company kept pace with the rapid development of the health sector in Saudi Arabia and gradually evolved to meet the needs and demands of a constantly growing market.
 </p>
 <p>
  <br/>
 </p>
 <p>
  Salehiya is based in three major cities: Riyadh, Jeddah, and Dammam. It also has branches around the kingdom to cover the whole market and provide prompt and efficient client services, with over 1000 workforce.
 </p>
 <p>
  <br/>
 </p>
 <p>
  For more information, you can visit our website: www.salehiya.com
 </p>
 <p>
  <br/>
 </p>
 <p>
  <strong>
   Why Work with Us:
  </strong>
 </p>
 <p>
  Salehiya Healthcare is committed to creating a diverse and inclusive workplace where all employees are valued and respected. We believe in fostering a culture that encourages creativity and innovation, particularly in technology. We utilize the latest tools in our field and stay ahead of industry trends. Our comprehensive training programs and mentorship opportunities are designed to support professional growth and development. We prioritize maintaining a welcoming atmosphere for everyone.
 </p>
 <p>
  <br/>
 </p>
 <p>
  The core values that guide our people derive from our purpose to elevate the healthcare experience in the kingdom.
 </p>
 <p>
  <br/>
 </p>
 <p>
  <strong>
   Job Purpose:
  </strong>
 </p>
 <p>
  As a Marketing Associate, you will support the implementation of retail and aesthetic consumer brand strategies within the Saudi Arabian market. The role focuses on executing actionable plans that align with the brand&rsquo;s vision, bridging the gap between clinical efficacy and consumer marketing through operational support in product launches, market research, and integrated omnichannel execution.
 </p>
 <p>
  <br/>
 </p>
 <p>
  <strong>
   Key Responsibilities:
  </strong>
 </p>
 <p>
  <strong>
   Operational
  </strong>
 </p>
 <ul>
  <li>
   Support the identification of consumer needs and contribute to maintaining customer loyalty programs to assist in driving business success and growth within the Consumer Health sector.
  </li>
  <li>
   Collaborate in the implementation of tactical plans and provide operational support to the marketing team to enhance brand awareness, drive revenue, and ensure the success of marketing campaigns.
  </li>
  <li>
   Develop a clear understanding of the business's revenue and profitability drivers.
  </li>
  <li>
   Contribute to the execution of business strategies and roadmaps by providing necessary administrative and research support.
  </li>
  <li>
   Assist in market research, pricing analysis, and product development support for new and existing initiatives.
  </li>
  <li>
   Help implement marketing strategies across various channels, including traditional trade, modern trade, e-commerce, and emerging platforms.
  </li>
  <li>
   Assist with data collection and analysis to support business operations and decision-making
  </li>
  <li>
   Support the logistics and coordination of training sessions for Healthcare Professionals (HCPs), customers, and internal stakeholders.
  </li>
  <li>
   Assist in the planning, development, and execution of integrated marketing campaigns across multiple channels.
  </li>
  <li>
   Conduct research on target markets, demographics, competitors, and industry trends to provide actionable insights for the Marketing Manager.
  </li>
  <li>
   Work with agencies to coordinate the creation of engaging marketing materials, including blog posts, social media content, and brochures.
  </li>
  <li>
   Monitor and track sell-out data, stock levels, and marketing metrics to help evaluate campaign performance and identify trends.
  </li>
  <li>
   Assist in expanding consumer reach through the coordination of digital marketing activities and endorsements by HCPs and influencers.
  </li>
  <li>
   Provide end-to-end support in planning and executing marketing events, such as trade shows, exhibitions, webinars, and product launches.
  </li>
  <li>
   Maintain effective communication with internal stakeholders and work closely with cross-functional teams to ensure alignment.
  </li>
 </ul>
 <p>
  <br/>
 </p>
 <p>
  <strong>
   Qualifications:
  </strong>
 </p>
 <p>
  <strong>
   Minimum Qualifications:
  </strong>
 </p>
 <p>
  Bachelor&rsquo;s degree in Marketing, Business Administration, Pharmacy, or a related field.
 </p>
 <p>
  <strong>
   Minimum Experience:
  </strong>
 </p>
 <p>
  1-3 years of Previous marketing experience in the healthcare sector.
 </p>
 <p>
  <strong>
   Skills:
  </strong>
 </p>
 <ul>
  <li>
   Basic skills in coordinating multiple projects and meeting deadlines
  </li>
  <li>
   Proficiency in Microsoft Office (Excel for data analysis and PowerPoint for presentations).
  </li>
  <li>
   Familiarity with social media management, SEO basics, and working with digital influencers.
  </li>
  <li>
   Ability to track KPIs, monitor stock levels (Sell-out/Sell-in), and generate basic performance reports.
  </li>
 </ul>
</div>


Marketing Associate

CTI Clinical Trial and Consulting

<div><div><b>Clinical Research Associate (level dependent on experience)</b><br>
<br>
<b>Job Purpose/Summary</b></div>
<div><br>
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.</div>
<div></div><div><b>What You&rsquo;ll Do</b></div>
<ul><li>Conduct evaluation, initiation, monitoring and close out visits</li>
<li>Assist with regulatory and study start-up activities including contract and budget negotiations</li>
<li>Ensure clinical data integrity and meet study timelines</li>
<li>Provide ongoing updates and support to project management</li>
<li>Attend global project meetings including investigator meetings and global team teleconferences</li>
<li>Complete assigned training programs in drug development processes, therapeutic areas, Good Clinical Practices (GCPs) and any applicable local regulatory requirements.</li>
</ul><div><b>What You Bring</b></div>
<ul><li>2 - 3 years of clinical research experience as a CRA or related profession</li>
<li>Life science background</li>
<li>Excellent knowledge in ICH-GCP and regulatory requirement</li>
<li>Fluent in English</li>
</ul><div><b>Why CTI?</b></div>
<div>At CTI, we recognize that our people are what make our company successful. Our work moves medicine forward.</div>
<div></div><div>For that reason, we treat our team members with the respect they deserve, and our numbers show it:</div>
<ul><li>We support career progression &ndash; 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</li>
<li>We value education and training &ndash; We provide tuition assistance, partner with universities and colleges to create programs in our field, and have a dedicated training department</li>
<li>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.</li>
<li>Our culture is unparalleled &ndash; 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</li>
<li>We think globally and act locally &ndash; 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.</li>
<li>We are looking toward the future &ndash; 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</li>
<li>Our work makes a difference &ndash; 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</li>
</ul><div><div><div><div>Are you interested? Then we look forward to your electronic application, with a tabular CV in English.<br>
<br>
<b>CTI Clinical Trial and Consulting Services</b><br>
<br>
Filipa Magalh&atilde;es<br>
<br>
www.ctifacts.com</div></div></div></div></div>

Clinical Research Associate (level dependent on experience)

Explore 878+ Clinical research manager in Riyadh this April. Find roles across top companies and apply now to boost your career.