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clinical research associate

Bristol Myers Squibb

<div>Working with Us 
Challenging. Meaningful. Life-changing. Those aren't words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You'll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams. Take your career farther than you thought possible. 
 
Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives. Read more: careers.bms.com/working-with-us . 
 
Job Description<ul><li>
Conduct site qualification, initiation, routine monitoring and close-out visits across all trial phases in accordance with the Site Monitoring Plan, ensuring adherence to protocol, BMS Standard Operating Procedures (SOPs) and ICH GCP</li><li>
Maintain the ethical and scientific integrity of clinical trials by verifying data within electronic systems and paper records (as applicable) to ensure the accessibility, completeness and accuracy of data submitted by study sites</li><li>
Conduct site qualification, initiation, routine monitoring and close-out visits across all trial phases in accordance with the Site Monitoring Plan, ensuring adherence to protocol, BMS Standard Operating Procedures (SOPs) and ICH GCP</li><li>
Monitor site adherence to ICH GCP and local regulations, including compliance with the principles of ALCOA to maintain data integrity and reliability. Where required, provide training and support to site staff to uphold these standards and ensure patient safety. Participate in sponsor and/or Health Authority audits and inspections as applicable.</li><li>
Cultivate and sustain effective relationships with internal cross-functional teams and external partners, including vendors, clinical sites, and key stakeholders. Serve as the organization's representative for clinical trials at the site level.</li><li>
Motivate and influence sites to meet study objectives, including enrollment and retention goals.</li><li>
Communicate effectively, adapting to meet the needs of different stakeholders, utilizing the most appropriate communication style and method. Prepare and submit written reports, both monitoring and administrative, in a timely, accurate, concise, professional and objective manner</li><li>
Assess potential Investigators and their sites to ensure sufficient resources and capabilities to conduct clinical trials. May identify new potential Investigators and/or sites through ongoing collaborations with internal and external stakeholders during the site feasibility and selection process.</li><li>
Demonstrate understanding and proficiency working with targeted, centralized, remote and riskbased monitoring approaches</li><li>
Identify, assess, and prioritize risks at the site and study level and support sites in mitigating issues, including implementing mitigation strategies based on risk indicators</li><li>
Utilize strong analytical skills to evaluate site data and operational metrics, including ability to adjust monitoring strategies based on data trends and site performance</li><li>
Where applicable, perform Unblinded Site Monitor activities to protect the blind of the study by acting as secondary monitoring source separate from the blinded monitor</li><li>
Accountable for the review, reconciliation, and oversight of study drug/IMP. May support study drug/IMP label translation needs as applicable.</li><li>
Involvement in Regulatory Compliance audit/inspection process, as needed. This includes the development and implementation of site corrective and preventive actions.</li><li>
In specific instances, may support start-up and submission related activities, including ICF reviews and collection of documents to/from site.</li><li>
Support provision of access to relevant BMS and vendor systems is available for clinical trial site personnel and ensures internal BMS systems are kept up to date for site monitoring activities.</li><li>
Support coordination of site activities related to database locks to ensure timelines are met as required locally.</li><li>
Perform timely site closure activities when all required protocol visits and follow-up are completed.</li></ul>
Qualifications &amp; Experience 
 
Degree/Certification/Licensure:
 
 
<ul><li>Bachelor's degree required, preferably within life sciences or equivalent</li></ul> 
<ul><li>Valid driver's license (as locally required)</li></ul> 
Experience: 
 
<ul><li>2-3 years of relevant clinical research experience, able to work independently, demonstrates proficiency in all aspects of the role</li></ul> 
<ul><li>Relevant prior Pharma/Biotech Sponsor employment or experience as a clinical study coordinator</li></ul> 
preferred 
 
<ul><li>Experience in the drug discovery/development process.</li></ul> 
Competencies: 
 
<ul><li>Knowledge and understanding of clinical research processes, regulations and methodology</li></ul> 
<ul><li>Understands clinical landscape with practical knowledge of a variety of medical settings and medical records management</li></ul> 
<ul><li>Working knowledge of ICH/GCP Guidelines and applicable local laws and regulations (that govern</li></ul> 
clinical trials, with the ability to apply regulatory requirements to ensure compliance in clinical research activities (Analytical thinking/critical thinking skills. Capable of using technology to analyze 
 
diverse and complex data sets, identify issues, trends, and outliers to develop effective solutions 
 
(Demonstrate adaptability and a growth mindset by quickly learning and applying new technologies, 
 
embracing evolving methodologies, and remaining open to innovative ways of working in a dynamic 
 
environment 
 
<ul><li>Organization and time management skills</li></ul> 
<ul><li>Ability to build, maintain and strengthen relationships even under pressure and/ or in difficult situations with internal and external stakeholders</li></ul> 
<ul><li>Good verbal and written communication skills (both in English and local language)</li></ul> 
<ul><li>Have a foundational level of disease understanding and awareness (how the protocol fits in current</li></ul> 
landscape, standard of care, etc.) 
 
<ul><li>Proven ability to work independently with a high degree of autonomy, proactively managing tasks and</li></ul> 
seeking opportunities for continuous learning 
 
<ul><li>Ability to manage multiple protocols, across multiple therapeutic areas, which may require travel,</li></ul> 
based upon assigned site location and/or geographic territory 
 
<ul><li>Proficient in navigating and utilizing multiple clinical systems (e.g., CTMS, eTMF, RBQM dashboards) to</li></ul> 
identify and resolve issues, support site performance, and ensure data integrity 
 
Software that must be used independently and without assistance (e.g., Microsoft Suite) 
 
<ul><li>Microsoft Suite</li></ul> 
<ul><li>Clinical Trial Management Systems (CTMS)</li></ul> 
<ul><li>Electronic Data Capture Systems (eDC)</li></ul> 
<ul><li>Electronic Trial Master File (eTMF)</li></ul> 
<ul><li>RBM tools and platforms (e.g., Veeva, Medidata, CluePoints).</li></ul> 
If you come across a role that intrigues you but doesn't perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career.
 
 
Uniquely Interesting Work, Life-changing Careers 
With a single vision as inspiring as Transforming patients' lives through science&trade; , every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in a supportive culture, promoting global participation in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues. 
 
On-site Protocol 
 
BMS has an occupancy structure that determines where an employee is required to conduct their work. This structure includes site-essential, site-by-design, field-based and remote-by-design jobs. The occupancy type that you are assigned is determined by the nature and responsibilities of your role:
 
 
Site-essential roles require 100% of shifts onsite at your assigned facility. Site-by-design roles may be eligible for a hybrid work model with at least 50% onsite at your assigned facility. For these roles, onsite presence is considered an essential job function and is critical to collaboration, innovation, productivity, and a positive Company culture. For field-based and remote-by-design roles the ability to physically travel to visit customers, patients or business partners and to attend meetings on behalf of BMS as directed is an essential job function.
 
 
BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace accommodations/adjustments and ongoing support in their roles. Applicants can request a reasonable workplace accommodation/adjustment prior to accepting a job offer. If you require reasonable accommodations/adjustments in completing this application, or in any part of the recruitment process, direct your inquiries to adastaffingsupport@bms.com . Visit careers.bms.com/ eeo -accessibility to access our complete Equal Employment Opportunity statement.
 
 
BMS cares about your well-being and the well-being of our staff, customers, patients, and communities. As a result, the Company strongly recommends that all employees be fully vaccinated for Covid-19 and keep up to date with Covid-19 boosters.
 
 
BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area. 
 
If you live in or expect to work from Los Angeles County if hired for this position, please visit this page for important additional information: https://careers.bms.com/california-residents/
 
 
Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.</div>

Clinical Research Associate

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/
 
 
 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)

<div>Job Title: Clinical Research Intern Business Introduction At GSK, we have bold ambitions for patients, aiming to positively impact the health of 2.5 billion people by the end of the decade. Our R&amp;D focuses on discovering and delivering vaccines and medicines, combining our understanding of the immune system with cutting-edge technology to transform people&rsquo;s lives. GSK fosters a culture ambitious for patients, accountable for impact, and committed to doing the right thing, making sure that we focus our efforts on accelerating significant assets that meet patients&rsquo; needs and have the highest probability of success. We&rsquo;re uniting science, technology, and talent to get ahead of disease together.
 
Find out more:
 
Our approach to R&amp;D Position Summary Join us as a Clinical Research Intern and be part of a team that&rsquo;s making a real difference in healthcare. In this role, you&rsquo;ll support clinical research activities, collaborate with cross-functional teams, and gain hands-on experience in a dynamic and inclusive environment. We&rsquo;re looking for individuals who are curious, detail-oriented, and eager to learn. This is your chance to grow, contribute to meaningful work, and help us achieve our mission of getting ahead of disease together. Responsibilities This role will provide YOU the opportunity to lead key activities to progress YOUR career. These responsibilities include some of the following: - Assist in the preparation and management of clinical trial documentation. - Support the coordination of logistics for clinical research activities. - Collaborate with internal teams and external research sites to ensure smooth operations. - Help maintain and update clinical databases and records. - Contribute to compliance with regulatory and ethical standards in clinical research. - Provide administrative support to the clinical research team. Basic Qualification We are seeking professionals with the following required skills and qualifications to help us achieve our goals: - Currently enrolled in a degree program in Life Sciences, Pharmacy, Medicine, or a related field. - Strong organizational skills and attention to detail. - Ability to work collaboratively in a team environment. - Proficiency in Microsoft Office tools (Word, Excel, PowerPoint). - Intermediate English language skills (written and spoken). - Availability to work part-time hours during weekdays. Preferred Qualification If you have the following characteristics, it would be a plus: - Previous experience or coursework in clinical research or healthcare. - Familiarity with regulatory guidelines and ethical standards in clinical trials. - Strong communication skills to interact with diverse stakeholders. - Problem-solving mindset and ability to adapt to new challenges. - Interest in pursuing a career in clinical research or the pharmaceutical industry. - Fluency in Turkish and English. This is an on-site role based in T&uuml;rkiye, with opportunities to learn and grow in a supportive and inclusive environment. Ready to take the next step in your career? Apply now and start your journey with GSK!
Why GSK?
 
Uniting science, technology and talent to get ahead of disease together.
GSK is a global biopharma company with a purpose to unite science, technology and talent to get ahead of disease together. We aim to positively impact the health of 2.5 billion people by the end of the decade, as a successful, growing company where people can thrive. We get ahead of disease by preventing and treating it with innovation in specialty medicines and vaccines. We focus on four therapeutic areas: respiratory, immunology and inflammation; oncology; HIV; and infectious diseases &ndash; to impact health at scale.
People and patients around the world count on the medicines and vaccines we make, so we&rsquo;re committed to creating an environment where our people can thrive and focus on what matters most. Our culture of being ambitious for patients, accountable for impact and doing the right thing is the foundation for how, together, we deliver for patients, shareholders and our people.
Contact information:
 
You may apply for this position online by selecting the Apply now button.
Important notice to Employment businesses/ Agencies
GSK does not accept referrals from employment businesses and/or employment agencies in respect of the vacancies posted on this site. All employment businesses/agencies are required to contact GSK's commercial and general procurement/human resources department to obtain prior written authorization before referring any candidates to GSK. The obtaining of prior written authorization is a condition precedent to any agreement (verbal or written) between the employment business/ agency and GSK. In the absence of such written authorization being obtained any actions undertaken by the employment business/agency shall be deemed to have been performed without the consent or contractual agreement of GSK. GSK shall therefore not be liable for any fees arising from such actions or any fees arising from any referrals by employment businesses/agencies in respect of the vacancies posted on this site.</div>

Clinical Research Intern

Fortrea

<div>We are recruiting for our sponsor-dedicated business in T&uuml;rkiye and are seeking to hire a CRA on a permanent, full-time contract.
Our positions offer excellent exposure to a range of disease areas, and a real opportunity for career progression and promotion in time.
At Fortrea, you will have autonomy to organize your work and in return, you will be supported and empowered to go beyond the typical CRA role, to really be an expert on your protocols and to own your sites.<h3 class="jobSectionHeader">
Summary of Responsibilities</h3><ul><li>
Manage all phases of clinical site activity: pre-study, initiation, monitoring, and close-out visits</li><li>
Ensure protocol compliance, data accuracy, patient safety, and audit readiness</li><li>
Review source documents, resolve data queries, and oversee SAE reporting and follow-up</li><li>
Act as primary liaison with sites, vendors, and internal teams</li><li>
Prepare trip reports and support regulatory submissions, feasibility, and site budget negotiations</li><li>
Mentor junior staff and support project coordination as assigned</li></ul><h3 class="jobSectionHeader">
Qualifications</h3><ul><li>
Degree in life sciences or related health profession</li><li>
Strong knowledge of regulatory requirements and clinical trial processes</li><li>
Fluent in English and local language (written and verbal)</li></ul><h3 class="jobSectionHeader"> 
Experience</h3><ul><li>
Minimum 1.5 years of clinical on-site monitoring in interventional studies</li><li>
Skilled in SAE handling, CRF review, and site management</li><li>
Able to work independently with strong planning and problem-solving skills</li><li>
Fluent in English and Turkish</li></ul>
Learn more about our EEO &amp; Accommodations request here.</div>

CRA II - Sponsor Dedicated

<div>Job Description
As GCTO T&uuml;rkiye, we provide our interns the opportunity to work on meaningful
assignments and make sure that they gain real world experiences (in the areas of
Regulatory &amp; Finance and Supply &amp; CRA support). 
As an intern, you may provide support to these areas; examples include;<ul><li>
Drug &amp; Non Drug Supply Management</li><li>
Payment and Invoice Management</li><li>
Document &amp; report checks from Veeva</li><li>
Preparation of submissions to regulatory authorities</li><li>
Management of safety documents</li><li>
Pre and Post Monitoring Visit Preparations</li><li>
Data Mining and Analysis in dashboards</li></ul> 
Qualifications:<ul><li>
4th years students or graduates from Science / Pharmacy Faculties</li><li>
Good command of written and spoken English is preferred</li><li>
Good command of MS Office applications</li><li>
Self motivated with good communication skills</li></ul>
Required Skills:
Clinical Research, Data Analysis, Data Science, Data Visualization, Detail-Oriented, Event Planning, Python (Programming Language), Software Proficiency
Preferred Skills:
Current Employees apply HERE
Current Contingent Workers apply HERE
Search Firm Representatives Please Read Carefully 
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.
Employee Status:
Intern/Co-op (Fixed Term)
Relocation:
VISA Sponsorship:
Travel Requirements:
Flexible Work Arrangements:
Hybrid
Shift:
Valid Driving License:
Hazardous Material(s):
Job Posting End Date:
10/14/2025<ul><li>A job posting is effective until 11:59:59PM on the day BEFORE the listed job posting end date. Please ensure you apply to a job posting no later than the day BEFORE the job posting end date. 
</li></ul> 
Requisition ID:R368742</div>

PSI CRO

<div>
 
 Company Description
 
 
 
 PSI is a leading full-service global Contract Research Organization providing a wide range of clinical trial services to the pharmaceutical and biotechnology industry, mainly for the development of clinical drugs. PSI has 3.000+ employees and 60+ affiliates in Europe, North and South America, Asia Pacific and South Africa.
 
 
 
 Job Description
 
 
 
 If you are a qualified enthusiastic legal professional, you may be the expert we are looking for to join our dynamic team in T&uuml;rkiye.
 
 
 This role supports PSI&rsquo;s Legal with a primary focus on contracts related to clinical research. As an Associate Legal Counsel, you will work closely with PSI&rsquo;s international legal and project teams in the review of contracts and to provide legal advice and support for Turkish office.
 
 
 
 The position is open to candidates from both Istanbul and Ankara
 
 .
 
 
 Your role will include:
 
 
 <ul>
 <li>
 Review, draft and negotiate contracts and other legal documents relating to clinical research.
 </li>
 <li>
 Adapt company contract templates to the requirements of clients, hospitals, investigators, medical specialists and vendors.
 </li>
 <li>
 Prepare, drafts and reviews corporate documents.
 </li>
 <li>
 Provides advice and support on compliance with clinical research legislation, company law, employment law, data protection and other legislation.
 </li>
 <li>
 Drafts, reviews, and updates PSI policies, procedures and instructions relating to legal matters and supports their implementation.
 </li>
 <li>
 Supports compliance with PSI policies, procedures, and instructions relating to legal matters.
 </li>
 <li>
 Provides training to other PSI departments.
 </li>
 <li>
 Researches, and analyses various legal matters.
 
 
 
 </li>
 </ul>
 
 Qualifications
 
 
 
 <ul>
 <li>
 Law degree, with sound knowledge of Turkish legislation and contract law
 </li>
 <li>
 A minimum of 4 years of experience in commercial legal practice (law firm or consulting), ideally with exposure to the pharmaceutical sector
 </li>
 <li>
 Full professional proficiency in Turkish and English
 </li>
 <li>
 Good knowledge of commercial, corporate and contract law, as well as other relevant legislation (e.g. data protection; labor code)
 </li>
 <li>
 Advanced legal contract drafting and review skills
 </li>
 <li>
 Good communication, negotiations and organizational skills
 </li>
 <li>
 Ability to work accurately with strong attention to detail
 </li>
 <li>
 Excellent knowledge of the Microsoft Office package, in particular MS Word
 
 
 
 </li>
 </ul>
 
 Additional Information
 
 
 
 Make the right call and take your career to a whole new level. Join the company that focuses on its people and invests in their professional development and success.
</div>

Associate Legal Counsel

<div>Company Description 
PSI is a leading full-service global Contract Research Organization providing a wide range of clinical trial services to the pharmaceutical and biotechnology industry, mainly for the development of clinical drugs. PSI has 3.000+ employees and 60+ affiliates in Europe, North and South America, Asia Pacific and South Africa. 
Job Description 
If you are a qualified enthusiastic legal professional, you may be the expert we are looking for to join our dynamic team in T&uuml;rkiye.
This role supports PSI&rsquo;s Legal with a primary focus on contracts related to clinical research. As an Associate Legal Counsel, you will work closely with PSI&rsquo;s international legal and project teams in the review of contracts and to provide legal advice and support for Turkish office.
The position is open to candidates from both Istanbul and Ankara.
Your role will include:<ul><li>
Review, draft and negotiate contracts and other legal documents relating to clinical research.</li><li>
Adapt company contract templates to the requirements of clients, hospitals, investigators, medical specialists and vendors.</li><li>
Prepare, drafts and reviews corporate documents.</li><li>
Provides advice and support on compliance with clinical research legislation, company law, employment law, data protection and other legislation.</li><li>
Drafts, reviews, and updates PSI policies, procedures and instructions relating to legal matters and supports their implementation.</li><li>
Supports compliance with PSI policies, procedures, and instructions relating to legal matters.</li><li>
Provides training to other PSI departments.</li><li>
Researches, and analyses various legal matters.</li></ul> 

Qualifications 
<ul><li>
Law degree, with sound knowledge of Turkish legislation and contract law</li><li>
A minimum of 4 years of experience in commercial legal practice (law firm or consulting), ideally with exposure to the pharmaceutical sector</li><li>
Full professional proficiency in Turkish and English</li><li>
Good knowledge of commercial, corporate and contract law, as well as other relevant legislation (e.g. data protection; labor code)</li><li>
Advanced legal contract drafting and review skills</li><li>
Good communication, negotiations and organizational skills</li><li>
Ability to work accurately with strong attention to detail</li><li>
Excellent knowledge of the Microsoft Office package, in particular MS Word</li></ul> 

Additional Information 
Make the right call and take your career to a whole new level. Join the company that focuses on its people and invests in their professional development and success.</div>

Explore 353+ Clinical research associate in Istanbul this October. Find roles across top companies and apply now to boost your career.

353 clinical research associate jobs IN Istanbul

Clinical Research Associate

Clinical Research Associate (Biopharma)

Clinical Research Intern

CRA II - Sponsor Dedicated

Clinical Research Intern

Associate Legal Counsel

Associate Legal Counsel