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clinical research associate biopharma

AstraZeneca

<div>
 At AstraZeneca, we unlock the power of what science can do. Empowered to explore, everyday we work towards our ultimate aim &ndash; treating, preventing, modifying and even curing complex diseases. With an unwavering belief in following the science, we unleash our curiosity. Investing in key areas, harnessing innovative technologies and taking smart risks. Help to shape the future of healthcare as we take our pipeline from strength to strength. Embrace an environment built on lifelong learning. Never complacent, we seek opportunities to expand our knowledge. The place to build a long-term meaningful career. Here we get to develop and grow &ndash; whether that&rsquo;s working at the leading-edge or on varied stages and molecules. Working on things that have never been done before. In return, when great science comes alive, we have the opportunity to get published. We stand together behind a shared ambition. United by our collective passion for having a positive impact on patients&rsquo; lives. Important work that is both meaningful and fulfilling. With the potential to reach over a billion patients across the globe who are living with these complex diseases.
 
 
 
 Background &amp; Qualifications
 
 
 
 <ul>
 <li>
 University degree, preferably from Healthcare related areas (Pharmacy, Veterinary, Chemistry, Biology, Medical etc. Faculties),
 </li>
 <li>
 Good level of English,
 </li>
 <li>
 Minimum 1 year of experience in a CRA and/or study coordinator positions
 </li>
 <li>
 Strong communication and negotiation skills,
 </li>
 <li>
 Ability to prioritize and handle multiple tasks,
 </li>
 <li>
 Effective planning and organizational skills with a result-oriented approach,
 </li>
 <li>
 Analytical thinking, critical reasoning ability,
 </li>
 <li>
 Good command of MS Office applications,
 </li>
 <li>
 No restriction to travel,
 </li>
 <li>
 Driving License,
 </li>
 <li>
 No military obligation for male candidates.
 
 
 </li>
 </ul>
 
 Job Description
 
 
 
 <ul>
 <li>
 Perform monitoring and site management activities for phase trials projects to assess the progress of clinical projects at assigned investigative/physician sites
 </li>
 <li>
 Ensure clinical project is conducted, recorded, and reported in accordance with the protocol, Company SOPs, ICH-GCP, and all applicable local and legal requirements.
 </li>
 <li>
 May assume clinical functional leadership tasks are assigned, actions as Lead CRA for project
 </li>
 <li>
 Train, support and advise Investigators and site staff in study related matters, including Risk Based Quality Management (RbQM) principles.
 </li>
 <li>
 Drive performance at the sites. Proactively identify and ensure timely resolution to study-related issues and escalate them as appropriate.
 </li>
 <li>
 Perform regular Site Quality Risk Assessments and adapt monitoring intensity accordingly during the study.
 </li>
 <li>
 Ensure data query resolution in a timely manner.
 </li>
 <li>
 Work with data management to ensure the robust quality of the collected study data.
 </li>
 <li>
 Collaborate with local MSLs as directed by LSM or line manager.
 
 
 </li>
 </ul>
 
 Why AstraZeneca?
 
 
 
 A high performing team, we work hard to not just meet but go beyond the needs of patients and the wider healthcare industry We leverage our partnerships with external experts across the industry, to create and communicate evidence that changes medical practice. As a partner for many, we effectively communicate complex ideas whilst seeking to understand ever-changing needs and requirements. Our valuable contribution and scientific expertise is responsible for advancing our pipeline and accelerating our pathway to finding a cure. Are you already imagining yourself joining our team? Good, because we can&rsquo;t wait to hear from you.
 
 
 
 Where can I find out more?
 
 
 
 Follow AstraZeneca on LinkedIn https://www.linkedin.com/company/1603/
 
 
 Follow AstraZeneca on Instagram https://www.instagram.com/astrazenecaturkiyekariyer/
 
 
 
 Date Posted
 
 
 
 23-Tem-2025
 
 
 
 Closing Date
 
 
 
 AstraZeneca embraces diversity and equality of opportunity. We are committed to building an inclusive and diverse team representing all backgrounds, with as wide a range of perspectives as possible, and harnessing industry-leading skills. We believe that the more inclusive we are, the better our work will be. We welcome and consider applications to join our team from all qualified candidates, regardless of their characteristics. We comply with all applicable laws and regulations on non-discrimination in employment (and recruitment), as well as work authorization and employment eligibility verification requirements.
</div>

Clinical Research Associate (Biopharma)

Sanofi

<div><div>Pharmacovigilance Specialist - VIE Contract</div><div><ul><li>
Location: T&uuml;rkiye, Istanbul</li><li>
Target start date: 01/05/2026</li></ul></div>
iMove, the Sanofi VIE Program, is available to citizens of the European Economic Area (EU + Norway, Liechtenstein and Iceland) aged between 18 and 28.
PLEASE NOTE that since this program is primarily an international development program, candidates cannot apply to a VIE assignment in their own country of citizenship.
PLEASE NOTE that applications that are only submitted in French cannot be considered by our non-French speaking partners at Sanofi worldwide. Therefore, only applications that are submitted in English will be considered. Please make sure to apply with your personal email address.
About the job
As Pharmacovigilance Specialist VIE within our Pharmacovigilance team, you&rsquo;ll
support the department for the medicinal safety related activities and gain experience in pharmacovigilance.
This is an excellent opportunity for a recent graduate or early-career professional to gain valuable international experience in drug safety and pharmacovigilance within a leading global pharmaceutical company, Sanofi.
Join the engine of Sanofi&rsquo;s mission &mdash; where deep immunoscience meets bold, AI-powered research. In R&amp;D, you&rsquo;ll drive breakthroughs that could turn the impossible into possible for millions.
Ready to get started?
About Sanofi
We&rsquo;re an R&amp;D-driven, AI-powered biopharma company committed to improving people&rsquo;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&rsquo;s lives.
Main responsibilities:
Safety Information Management<ul><li>
Managing the intake and processing of safety information received via phone and email in Turkish.</li><li>
Accurately entering and transferring pharmacovigilance cases to our global vendor or directly into the global PV database, and ensuring timely and compliant processing and Health Authority submission of all safety data.</li></ul>
Reporting &amp; Documentation<ul><li>
Compiling, reviewing, and maintaining comprehensive safety reports, managing systematic archiving of all PV-related documentation.</li><li>
Supporting the planning and submission of periodic safety update reports.</li></ul>
Stakeholder Collaboration<ul><li>
Liaising with the Global Pharmacovigilance department for case management and safety assessments, and coordinating with local vendors for regulatory submissions to the Turkish Health Authority (TITCK).</li><li>
Building effective working relationships with cross-functional teams.</li></ul>
Risk Management &amp; Compliance<ul><li>
Supporting the implementation and tracking of Risk Management Plans (RMP).</li><li>
Managing the distribution and tracking of educational materials for healthcare professionals and patients.</li><li>
Reviewing market research activities to ensure PV compliance.</li></ul>
About you
Experience:<ul><li>
Previous professional experience, ideally within the pharmaceutical industry.</li></ul>
Soft and technical skills:<ul><li>
Strong communication and interpersonal skills.</li><li>
Strong attention to detail, accuracy in data management, proactive mindset with problem-solving abilities.</li><li>
Excellent organizational and time management skills.</li><li>
Ability to work effectively in a multicultural team environment.</li><li>
Proven ability to meet deadlines and manage multiple priorities.</li><li>
Knowledge of pharmacovigilance regulations and guidelines and previous experience with safety databases or case processing systems would only be a plus.</li></ul>
Education:<ul><li>
Master's degree in Life Sciences, Pharmacy, Medicine, or related field is preferred.</li></ul>
Languages:<ul><li>
Fluency in both English and Turkish is mandatory (written and spoken).</li></ul>
Why choose us?<ul><li>
Be part of a pioneering biopharma company where patient insights shape drug development.</li><li>
Work at the forefront of AI-powered science that accelerates discovery and improves outcomes.</li><li>
Collaborate beyond your expertise, sparking new ideas with diverse, multidisciplinary teams.</li><li>
Be part of a pioneering biopharma company that engages patients early in drug development and uses their insights to design studies that reflect real-world needs.</li><li>
Work at the forefront of drug discovery, harnessing cutting-edge AI, data, and digital platforms to push the boundaries of science.</li><li>
Help improve the lives of millions of people globally by making drug development quicker and more effective.</li></ul><div>
iMove is a unique program tailored for European youth interested in challenging themselves with meaningful assignments across the globe. At Sanofi we have a strong ambition to invest in young talents who will drive the success of Sanofi tomorrow.</div><div>
Sanofi&rsquo;s Work Abroad Program, iMove, offers jobs-assignments with actual responsibilities and a perspective to grow. We provide those opportunities in various functions such as: marketing, finance, regulatory, supply chain, clinical trials, production, etc. and in more than 40 countries. Sanofi unites people who are passionate about solving healthcare needs across the world. Joining our iMove Work Abroad Program is a unique opportunity to make a difference through your work.</div><div> 
#LI-EUR
</div>null</div>

Pharmacovigilance Specialist - VIE Contract

Eli Lilly

<div>At Lilly, we unite caring with discovery to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our employees around the world work to discover and bring life-changing medicines to those who need them, improve the understanding and management of disease, and give back to our communities through philanthropy and volunteerism. We give our best effort to our work, and we put people first. We&rsquo;re looking for people who are determined to make life better for people around the world.<h3 class="jobSectionHeader">
Overview</h3>
The Clinical Research Lead (CRL) is responsible for managing clinical investigators and sites participating in Lilly clinical trials and/or Post-Marketing Safety Studies. This includes investigator/site identification and qualification, ensuring timely trial enrollment aligned with scientific objectives, database lock delivery, issue resolution at trial sites, and maintaining inspection readiness at all times.
The CRL ensures global program delivery through comprehensive investigator and site management, leveraging data and tools for informed decisions, and fostering high-quality interactions with clinical trial sites to provide an unparalleled customer experience. Additionally, the CRL oversees vendor monitoring activities, identifying and mitigating significant findings and trends.
In countries without an Associate Director/Director of Investigator Engagement, the CRL may represent Investigator Engagement internally and externally, including interactions with regulatory bodies and influencing the local regulatory environment and strategy.<h3 class="jobSectionHeader">
Primary Responsibilities</h3>
Clinical Investigator Management<ul><li>
Manage all activities at clinical trial sites, including site identification, qualification, enrollment planning, execution, and close-out.</li><li>
Ensure timely delivery of enrollment readiness, trial recruitment, and database locks through performance management and issue resolution.</li><li>
Identify opportunities to accelerate trial enrollment while maintaining an exceptional customer experience.</li><li>
Apply scientific, therapeutic area, and regional expertise to support trial execution and quality data delivery.</li><li>
Develop strategic institutional/site relationships to optimize clinical trial programs across therapeutic areas.</li></ul>
Clinical Trial Management<ul><li>
Implement investigator/site risk plans to meet enrollment and database lock commitments.</li><li>
Maintain site and country-level inspection readiness at all times.</li><li>
Use metrics to inform site/country/regional decision-making.</li><li>
Collaborate with internal and external teams to remove barriers to trial execution.</li><li>
Understand local treatment paradigms and standard of care to support feasibility and trial allocation.</li><li>
Provide vendor oversight for site monitoring activities.</li><li>
For countries with PMS requirements: manage Post-Marketing Safety Studies, including CRO selection, regulatory documentation, and project management.</li></ul>
Business Management and Engagement<ul><li>
Build strong professional relationships with clinical investigators to expand research partnerships and deliver an exceptional trial experience.</li><li>
Collaborate cross-functionally to align priorities and deliver the portfolio.</li><li>
Prospect targeted sites in line with portfolio strategy.</li><li>
Maintain therapeutic and technical expertise for scientific discussions with investigators and site staff.</li><li>
Act as a communication bridge between sites, vendors, and Lilly.</li><li>
Influence internal and external factors to improve clinical research delivery.</li></ul>
Country/Regulatory Responsibilities (where applicable)<ul><li>
Engage with regulatory bodies, ethical review boards, and national authorities to represent Lilly in the clinical trial environment.</li><li>
Participate in country pharmaceutical associations and affiliated bodies.</li><li>
Ensure compliance with local regulatory requirements and maintain internal processes accordingly.</li><li>
Contribute to external clinical development community initiatives and incorporate learnings into internal strategies.</li><li>
Support affiliate leadership in implementing regional initiatives.</li></ul><h3 class="jobSectionHeader">
Minimum Qualifications</h3><ul><li>
Bachelor&rsquo;s degree or equivalent (preferably in a scientific or health-related field).</li><li>
Minimum 3 years of experience in pharmaceutical industry and/or clinical research.</li><li>
Strong knowledge of Good Clinical Practice (GCP).</li><li>
Ability to acquire and maintain therapeutic expertise to support portfolio needs.</li><li>
Excellent organizational and self-management skills.</li><li>
Strong communication skills (verbal and written) and ability to influence others.</li><li>
Strategic agility and broad business acumen.</li><li>
Demonstrated leadership behaviors and ability to lead in uncertain environments.</li></ul><h3 class="jobSectionHeader">
Additional Preferences</h3><ul><li>
Strong organizational and planning skills.</li><li>
Ability to enhance customer experience.</li><li>
Fluent in English.</li><li>
Knowledge of country regulatory guidelines.</li><li>
Strong teamwork and interpersonal skills.</li><li>
Ability to develop innovative solutions.</li><li>
Travel required (50&ndash;75%).</li></ul>
Lilly is dedicated to helping individuals with disabilities to actively engage in the workforce, ensuring equal opportunities when vying for positions. If you require accommodation to submit a resume for a position at Lilly, please complete the accommodation request form (https://careers.lilly.com/us/en/workplace-accommodation) for further assistance. Please note this is for individuals to request an accommodation as part of the application process and any other correspondence will not receive a response.
Lilly does not discriminate on the basis of age, race, color, religion, gender, sexual orientation, gender identity, gender expression, national origin, protected veteran status, disability or any other legally protected status.
#WeAreLilly</div>

Clinical Research Lead

Fortrea

<div></div><div><div>Fortrea is recruiting an experienced Clinical Project Manager with valuable expertise in Oncology. In this role, you will ensure the successful execution of clinical studies on a local level, while maintaining high-quality standards and regulatory compliance. This position is sponsor-dedicated for a renowned pharmaceutical company.<div><div><div><div><div><div><div><div><div><h3 class="jobSectionHeader">
Please note this role is for upcoming future opportunities that may arise at Fortrea.
</h3></div></div></div></div></div></div></div></div></div></div>Summary of Responsibilities:<ul><li>
Leading the local study teams (consisting of monitors and study administrators) at country level to deliver committed components of clinical studies according to agreed resources, budget and timelines</li><li>
Ensuring that study sites are identified, site qualifications performed, set up, initiated, monitored, closed and documentation archived</li><li>
Ensuring timely submissions of proper application/documents to Ethic Committee/Regulatory Authority.</li><li>
Close communication with global study teams and overall responsibility for study commitments, for timely delivery of data to required quality as agreed with global</li><li>
Creating and implementing alternative action plans proactively in order to reach the targeted patient numbers; monitoring the patience admission processes in coordination with the researchers; planning and taking the necessary precaution when required</li><li>
Ensuring the compliance of the clinical research process with ICH-GCP practices, the study protocol, Global and Local Clinical SOP&rsquo;s, and the Ministry of Health Clinical Research Regulations; being knowledgeable about these procedures and keeping abreast of any changes and revision</li><li>
Participating in system/process improvement projects within global and local task groups consisting of employees from different units</li></ul>
Qualifications:<ul><li>
University degree, preferably from Healthcare related areas (Pharmacy, Veterinary, Chemistry, Biology, Medical etc. Faculties),</li><li>
Advanced level of English,</li><li>
Minimum 5 year experiences in Clinical Research (preferably 2 years in Project Management positions and Oncology specific)</li><li>
Project management skills,</li><li>
Strong communication and negotiation skills,</li><li>
Ability to prioritize and handle multiple tasks,</li><li>
Basic coaching skills and good at team work,</li><li>
Financial management skills,</li><li>
Effective planning and organizational skills with result-oriented approach,</li><li>
Stakeholder management experience,</li><li>
Analytical thinking, critical reasoning ability,</li><li>
Good command of MS Office applications,</li><li>
No restriction to travel,</li><li>
Driving License,</li></ul>
Learn more about our EEO &amp; Accommodations request here.</div>

Clinical Project Manager sponsor-dedicated

IQVIA

<div>
 
 IQVIA Laboratories
 
 
 
 IQVIA Laboratories is a global leader in drug discovery and development, offering comprehensive central and specialty biomarker services. Our expertise includes genomics, immunoassays, flow cytometry, anatomic pathology, precision medicine, vaccine assays, ADME, and bioanalytical services. We also specialise in antibody and biomarker discovery and decentralized clinical trial solutions. Committed to scientific rigor and operational excellence, we support all phases of drug development, ensuring high data integrity and accelerating transformative therapies.
 
 
 
 Join us on our exciting journey!
 
 
 
 
 Job Overview
 
 
 
 Define the scope and objectives of business systems through research and collaboration with stakeholders.
 
 
 Analyse user needs and adjust system logic to enhance efficiency and performance.
 
 
 Oversee business systems projects from inception through implementation and support.
 
 
 Design PowerBI dashboards and functional prototypes to support data-driven requirements gathering.
 
 
 Extract, query, and interpret complex lab data using SQL to inform clinical and operational decisions.
 
 
 Translate technical infrastructure requirements into accessible documentation and actionable plans.
 
 
 Foster cross-functional collaboration to align technology with business goals in clinical trial settings.
 
 
 
 Requirements
 
 
 
 <ul>
 <li>
 Bachelor&rsquo;s Degree in Computer Science or Life Sciences.
 </li>
 <li>
 10&ndash;15 years of experience in IT as a Business Analyst, including 6 years in a Central Lab or Clinical Trials environment preferred.
 </li>
 <li>
 Deep understanding of business applications and client requirements in a regulated setting.
 </li>
 <li>
 Strong SQL skills for querying and managing data in complex systems.
 </li>
 <li>
 Proficiency with PowerBI to translate datasets into dynamic visualizations and insights.
 </li>
 <li>
 Knowledge of lab data structures, enterprise platforms, and clinical research workflows.
 </li>
 <li>
 Exceptional communication, documentation, and coordination skills across technical and non-technical teams.
 
 
 </li>
 </ul>
 
 Benefits Of Joining IQVIA
 
 
 
 <ul>
 <li>
 Work-Life Balance, with a strong focus on a positive well-being.
 </li>
 <li>
 Continuous career development and growth opportunities.
 </li>
 <li>
 Variety of therapeutic areas
 </li>
 <li>
 Collaborative and supportive team environment
 </li>
 <li>
 Access to cutting-edge and innovative, in-house technology
 
 
 </li>
 </ul>
 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 https://jobs.iqvia.com
</div>

Senior Business Systems Analyst/Product Owner

Parexel

<div>Key Accountabilities:<div><div><div><div><div><div><div><div><div>
Site Management Responsibilities<ul><li>
Contributes to the selection of potential investigators.
</li><li>In some countries, as required, Sr CRAs are accountable for study start-up and regulatory maintenance. Tasks may include Site Qualification Visits, collection, preparation, review and tracking of documents for the application process; submission of proper application/documents to EC/IRB and to Regulatory Authorities for start-up and for the duration of the study.
</li><li>Trains, supports, and advises Investigators and site staff in study related matters, including Risk Based Quality Management (RbQM) principles.
</li><li>Confirms that site staff have completed and documented the required training appropriately, including ICH-GCP training, prior to and for the duration of the study. Ensures the sites are always inspection ready.
</li><li>Actively participates in Local Study Team (LST) meetings.
</li><li>Contributes to National Investigators meetings, as applicable.</li><li>
Initiates, monitors, and closes study sites in compliance with Client Procedural Documents. Shares information on patient recruitment and study site progress (site quality/performance) within the LST.
</li><li>Drives performance at the sites. Proactively identifies and ensures timely resolution to study-related issues and escalates them as appropriate.
</li><li>Updates CTMS and other systems with data from study sites as per required timelines.
</li><li>Manages study supplies (Investigator Site File (ISF), etc.), drug supplies and drug accountability at study site. Prepares study drug for destruction, if applicable.</li><li>
Performs monitoring visits (remote and onsite), as well as remote data checks, in accordance with the timelines specified in the study specific Monitoring Plan. If required, determines and discusses with LSAD the correct timing and type of visits.
</li><li>Performs Source Data Review (SDR), Case Report Form (CRF) review and Source Data Verification (SDV), in accordance with the Monitoring Plan.
</li><li>Performs regular Site Quality Risk Assessments and adapts monitoring intensity accordingly during the study.
</li><li>Ensures data query resolution in a timely manner.
</li><li>Works with data management to ensure robust quality of the collected study data.
</li><li>Ensures accurate and timely reporting of Serious Adverse Events and their follow ups.</li><li>
Prepares and finalizes monitoring visit reports in CTMS and provides timely feedback to the Principal Investigator, including follow-up letter, within required timelines and in line with Client SOP.
</li><li>Follows up on outstanding actions with study sites to ensure resolution in a timely manner.
</li><li>Follows quality issue processes by escalating systematic or serious quality issues, data privacy breaches, Clinical Study Protocol (CSP) or ICH-GCP compliance issues to Local Management and/or Clinical Quality Management (CQM) as required.
</li><li>Assists site in maintaining inspection ready ISF.
</li><li>Prepares for and collaborates with the activities associated with audits and regulatory inspections in liaison with LSAD and Clinical Quality Associate Director (CQAD).
</li><li>Ensures timely collection/uploading of essential documents into the eTMF in accordance with ICHGCP, Client SOPs and local requirements. Supports/participates in regular QC checks performed by LSAD or delegate.
 </li><li>Ensures that all study documents under their responsibility (i.e., site documents, relevant communications, etc.) are available and ready for final archiving and completion of local part of the eTMF.
</li><li>Provides feedback on any research related information including sites/investigators/competing studies that might be useful for the local market.
</li><li>Collaborates with local Medical Scientific Liaisons (MSLs) as directed by LSAD or line manager</li></ul>
Compliance with Sponsor Standards<ul><li>
Ensures compliance with the Client&rsquo;s Code of Ethics and company policies and procedures relating to people, finance, technology, security, and SHE (Safety, Health and Environment).</li><li>
Ensures compliance with local, national, and regional legislation, as applicable.
</li><li>Completes timesheets accurately as required</li></ul>
Compliance with Parexel Standards<ul><li>
Complies with required training curriculum.
</li><li>Completes timesheets accurately as required.
</li><li>Submits expense reports as required.
</li><li>Updates CV as required.
</li><li>Maintains working knowledge of and complies with Parexel/Client processes, ICH-GCPs and other applicable requirements.</li></ul>
Skills (Essential):
<ul><li>Excellent attention to detail.
</li><li>Good written and verbal communication skills.
</li><li>Good collaboration and interpersonal skills.
</li><li>Good negotiation skills.
</li><li>Proficient in written and spoken English language required.
</li><li>Fluency in local language(s) required.
</li></ul>Skills (Desirable):
<ul><li>Ability to work in an environment of remote collaborators. Manages change with a positive approach for self, team and the business. Sees change as an opportunity to improve performance and add value to the business.
</li><li>Ability to look for and champion more efficient and effective methods/processes of delivering quality clinical trials with reduced budget and in less time.
</li><li>Good analytical and problem-solving skills.
</li><li>Demonstrates ability to prioritize and manage multiple tasks with conflicting deadlines.
</li><li>Ability to understand the impact of technology on projects and to use and develop computer skills while making appropriate use of systems/software in an e-enabled environment.
</li><li>Team oriented and flexible; ability to respond quickly to shifting demands and opportunities Knowledge and Experience (Essential):
</li><li>Excellent knowledge of international guidelines ICH-GCP, basic knowledge of GMP/GDP. &bull; Good knowledge of relevant local regulations.
</li><li>Good medical knowledge and ability to learn relevant Client Therapeutic Areas.
</li><li>Basic understanding of the drug development process.
</li><li>Good understanding of Clinical Study Management including monitoring, study drug handling and data management.</li></ul>
Knowledge and Experience (Desirable):
<ul><li>Familiar with risk-based monitoring approach including remote monitoring.
</li><li>Good cultural awareness.
</li></ul>Education:
<ul><li>Bachelor&rsquo;s degree in related discipline, preferably in life science, (or equivalent adapted to local country market needs), that supports skills and capabilities of the position and ensures successful conduct of responsibilities and appropriate interactions with internal and or external customers.</li></ul>
Other:<ul><li>
Ability to travel nationally/internationally as required.
</li><li>Valid driving license per country requirements, as applicable</li></ul></div></div></div></div></div></div></div></div></div></div>

Senior Clinical Research Associate & CRAII - FSP (Open)

Sabancı University IMC - Integrated Manufacturing Technologies Research and Application Center

<div>
 
 Location:
 
 Sabanc&inodot; University, Istanbul, T&uuml;rkiye
 
 
 
 Application Deadline:
 
 01.05.2026
 
 
 
 Active Evaluation Process:
 
 will start on 20.12.2025 and continue until the positions are filled.
 
 
 
 Job Start Date (approximate):
 
 01.09.2026
 
 
 
 About Sabanc&inodot; University
 
 
 
 Established by the Sabanc&inodot; Foundation in 1994, Sabanc&inodot; University provides a world-class education to its students, from undergraduate to the PhD level. The university is distinguished by its innovative educational system, which is unique in T&uuml;rkiye. Sabanc&inodot; University began to accept students in 1999. It offers students the freedom to choose their academic program within the first two years of enrollment. As of 2012, Sabanc&inodot; University is recognized as the most entrepreneurial and innovative foundation university in the University Entrepreneurship and Innovation Index, which is an index created by the Ministry of Science, Industry, and Technology of T&uuml;rkiye. In addition, SU is one of the highest-ranked universities in the Times Higher Education World University Rankings in T&uuml;rkiye. As a young university, Sabanc&inodot; University aspires to become an international reference point for innovation in education and research.
 
 
 
 Position Overview
 
 
 
 The Electronics Engineering Program in the Faculty of Engineering and Natural Sciences (FENS) at Sabanci University invites applications for full-time faculty positions at all ranks. Junior candidates should have a Ph.D. degree in related fields from one of the top 300 universities for the research dimension according to the Times Higher Education World University Rankings&rsquo; 2024 list and high potential in research and teaching, and Senior candidates (Associate and Full Professor) are expected to have demonstrated academic leadership and a strong record of publications, teaching, research, and services.
 
 
 Applications are sought in all areas of Electronics Engineering such as but not limited to: Digital Integrated Circuits and Systems (VLSI, SoC, ASIC) and Semiconductor Optoelectronics or Photonics.
 
 
 The Electronics Engineering (EE) Program offers B.Sc., M.S., and Ph.D. degrees in Electronics Engineering and the B.Sc. program is accredited by MUDEK, part of the International Engineering Alliance - Washington Accord. In addition, the EE program is ranked as one of the top EE programs in Turkey by THE and QS ranking systems.
 
 
 Detailed information about the Electronics Engineering Program can be found at http://ee.sabanciuniv.edu/.
 
 
 
 Key Responsibilities
 
 
 
 
 Teaching:
 
 The candidate is expected to teach at undergraduate and graduate levels (the expected load is three courses per year) and supervise undergraduate student projects and graduate theses. Other responsibilities include curriculum assessment and development and developing innovative practices in teaching.
 
 
 
 Research:
 
 The candidate must develop a robust research agenda and supervise graduate students. The candidate is expected to apply for grants to national and international agencies to support this research agenda.
 
 
 
 Service:
 
 The candidate is expected to actively work in the committees to help improve the academic and administrative processes of the faculty and the university.
 
 
 
 Qualifications
 
 
 
 <ul>
 <li>
 Possess a Ph.D. Degree in Electrical or Electronics Engineering Programs.
 </li>
 <li>
 Strong research background as demonstrated by a publication record in high quality journals in the field.
 </li>
 <li>
 For candidates at the Assistant Professor level, post-doctoral research experience is required.
 
 
 </li>
 </ul>
 
 Why Join Sabanc&inodot; University?
 
 
 
 <ul>
 <li>
 Innovative Academic Environment: Sabanc&inodot; University is a leading private institution in Istanbul, known for its world-class research facilities, with its main campus located in Tuzla, a serene suburb of the city.
 </li>
 <li>
 Dynamic Research Community: Engage in groundbreaking research within a vibrant and collaborative academic community. Sabanc&inodot; University not only fosters a dynamic research culture with extensive international collaborations and access to global networks but also actively supports faculty applications to major international research programs such as ERC, MSCA, and Horizon Europe through its Research Support Office, with substantial internal funding for the project preparation phase.
 </li>
 <li>
 Career Development &amp; Mentorship: Benefit from career development programs and mentorship from distinguished researchers, supporting your growth in academia.
 </li>
 <li>
 Tenure Track: We offer a tenure-track position fully compatible with international standards, for junior faculty members. Tenure may be awarded in the fourth year of the initial contract contingent upon strong performance and demonstrated excellence in research, teaching, and service.
 </li>
 <li>
 SUCool Incubation Center: Opportunity to join the entrepreneurship ecosystem providing generous start-up funds, training and mentoring, global business and customer development, investor access and legal support, access to national and international grant funds and Sabanc&inodot; University PR support.
 
 
 </li>
 </ul>
 
 Compensation And Benefits Package
 
 
 
 <ul>
 <li>
 Competitive Salary: A highly competitive salary based on your qualifications and experience. Salary is reviewed based on annual performance results, and annual salary increases are compatible with academic performance.
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 Comprehensive Benefits: Enjoy private health insurance for you and your family, private pension plan contributions, life insurance, fully furnished on-campus housing or rental support.
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 Start-up Research Support: All newly starting faculty members are eligible for a substantial funding package (under the title &ldquo;Integration Fund&rdquo;) to initiate their research activities.
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 Access to Presidential Research Fund: During the first two years of their engagement at Sabanc&inodot; University, new faculty members are eligible to apply for the Presidential Research Fund support, which provides significant internal funding for preparing long-term research proposals.
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 Reduced Teaching Load: Newly starting faculty members benefit from a reduced teaching load during the first two years (Assistant Professor level) / first one year (Associate / Full Professor level)
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 Continued Research Support: All faculty members receive an annual Personal Research Fund to support their ongoing research activities, allocated laboratory space, and cutting-edge research facilities.
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 Tuition Assistance: Full-time faculty members receive a 50% reduction of tuition fees for their children or spouses for all undergraduate and graduate programs at Sabanc&inodot; University.
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 Education Support: Full-time faculty members receive tuition assistance for their dependent children who attend private / charter schools, from first through twelfth grade.
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 Relocation Allowance: Relocation allowance and an excess baggage / airfreight allowance for applicants recruited from overseas.
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 Additional Perks: Access to a discounted (42%) on-campus kindergarten, Health Center &amp; medical services and sports center.
 
 
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 </ul>
 
 Application Process
 
 
 
 
 Interested Applicants Should Submit With a Cover Letter
 
 
 
 <ul>
 <li>
 Detailed CV,
 </li>
 <li>
 a research statement outlining the envisioned research activities at Sabanc&inodot; University,
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 a teaching statement (in addition to the teaching philosophy, approach and experiences, the teaching statement should also include a list of all courses the candidate can offer at both graduate and undergraduate levels),
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 <li>
 three letters of reference using the online application form at http://crm.sabanciuniv.edu/academiccv/application.php?advertcode=EE-1-2025 .
 
 
 </li>
 </ul>
 
 Sabanc&inodot; University is committed to the principle of equal opportunity and equal treatment in education and employment. The University respects all individuals without any discrimination of gender, religion, national and ethnic origin, race, color, physical disability, physical appearance, marital or parental status, sexual orientation, age, or political affiliation in the administration of its educational, admission and employment policies, and its scholarship and university-sponsored programs.
 
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Full-time Faculty Member in Electronics Engineering Program(EE-1-2025)

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