regulatory affairs specialist Jobs in Istanbul

regulatory affairs specialist

associate - hr analytics Jobs in Istanbul

associate - hr analytics

associate-regional marketing Jobs in Istanbul

associate-regional marketing

clinical research associate (biopharma) Jobs in Istanbul

clinical research associate (biopharma)

principal research engineer Jobs in Istanbul

principal research engineer

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)

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

BioMarin Pharmaceutical Inc.

<div>
 Who We Are
 
 
 BioMarin is a global biotechnology company that relentlessly pursues bold science to translate genetic discoveries into new medicines that advance the future of human health.
 
 
 Since our founding in 1997, we have applied our scientific expertise in understanding the underlying causes of genetic conditions to create transformative medicines, using a number of treatment modalities.
 
 
 Using our unparalleled expertise in genetics and molecular biology, we develop medicines for patients with significant unmet medical need. We enlist the best of the best &ndash; people with the right technical expertise and a relentless drive to solve real problems &ndash; and create an environment that empowers our teams to pursue bold, innovative science. With this distinctive approach to drug discovery, we&rsquo;ve produced a diverse pipeline of commercial, clinical and preclinical candidates that have well-understood biology and provide an opportunity to be first-to-market or offer a substantial benefit over existing therapeutic options.
 
 
 
 About Worldwide Research And Development
 
 
 
 From research and discovery to post-market clinical development, our WWRD engine involves all bench and clinical research and the associated groups that support those endeavors. Our teams work on developing first-in-class and best-in-class therapeutics that provide meaningful advances to patients who live with genetic diseases.
 
 
 Regulatory Affairs Associate - Turkey
 
 
 <ul>
 <li>
 Fixed Term Temporary position for up to 7 months (Maternity Leave Cover)
 </li>
 <li>
 Bachelors degree in Pharmacy, Chemical Engineering, Chemistry.
 </li>
 <li>
 Minimum 1 years of Regulatory Affairs experience in a pharmaceutical company,
 </li>
 <li>
 Excellent command of English (both written and spoken),
 </li>
 <li>
 Strong commitment to compatibility, scientific quality and integrity
 </li>
 <li>
 Analytical thinking
 </li>
 <li>
 Good communication and teamwork collaboration
 </li>
 <li>
 Good detail-capturing skills while working in a fast-moving environment
 </li>
 <li>
 Role is based in Turkey
 
 
 </li>
 </ul>
 
 Job Description
 
 
 
 <ul>
 <li>
 Submission of Health Authority applications for registered and non-registered products and follow approval process. (GMP applications, new Marketing Authorization (MA) application, renewal submissions, lifecycle activities etc.)
 </li>
 <li>
 Compile all required documents received from Global Headquarters and prepare submission dossiers according to local requirements and make timely applications.
 </li>
 <li>
 Conduct the correspondences for all registered/non-registered products and follow up the Health Authority processes.
 </li>
 <li>
 Assist in managing global/local projects.
 </li>
 <li>
 Ensure the databases are updated on a timely basis.
 </li>
 <li>
 Evaluate local regulations/guidance for impact to any complex submission (e.g., MA, GMP) while ensuring that elements, quality, accuracy and format of regulatory submissions comply with applicable laws and regulatory standards.
 
 
 </li>
 </ul>
 Note: This description is not intended to be all-inclusive, or a limitation of the duties of the position. It is intended to describe the general nature of the job that may include other duties as assumed or assigned.
 
 
 Equal Opportunity Employer/Veterans/Disabled
 
 
 An Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, or protected veteran status and will not be discriminated against on the basis of disability.
</div>

Regulatory Affairs Associate - (Fixed Term Maternity Cover)

Medtronic

<div>At Medtronic you can begin a life-long career of exploration and innovation, while helping champion healthcare access and equity for all. You&rsquo;ll lead with purpose, breaking down barriers to innovation in a more connected, compassionate world.
<h1 class="jobSectionHeader">A Day in the Life
</h1>Careers That Change Lives
Join a mission-driven industry leader in medical technology and solutions to help drive innovation and transform the healthcare landscape. As Clinical Research &amp; Medical Sciences Director you will oversee both clinical and medical sciences aspects of running the medical organization in the TuRMECA region. Reporting to Chief Medical Officer Global Regions and VP Clinical Research &amp; Medical Sciences, you will lead the development and execution of clinical research and medical sciences agenda in TuRMECA region to enable patient access to innovative medical technologies.
A Day in Life
<ul><li>Provides Clinical/Medical Leadership at Business Reviews and discussions with the respective Country Leaders in the TuRMECA region.
</li><li>As a Leader within the TuRMECA regional organization, contributes to the development of a Clinical &amp; Medical affairs strategy and execute them in their sub-region.
</li><li>Is seen as the Voice of the Patient and the HCP.
</li><li>Provides Strategic Leadership for the development of Clinical strategy across OUs relevant to the region in Medtronic sponsored studies, Collaborative Research and ERPs including execution of Clinical Research and Medical Affairs.
</li><li>Ensures that the studies are scientifically valid and meet all relevant regulatory requirements and be conducted within ethical guidelines.
</li><li>Leads execution for both local and global studies, manages clinical research projects across Medtronic therapies across multiple businesses.
</li><li>Ensures that all clinical studies are published based on a fair assessment of the safety and efficacy of the tested product (s) and attainment of product approvals in a timely matter.
</li><li>Partners with the OUs/Marketing regionally to seek insights and disseminate the published data both globally and regionally. This may be done through Advisory Boards (ABs) to seek advice, Focus Group Discussions (FGDs), Continuing Medical Education (CMEs), Round Table Discussions (RTDs), and webinars for safe and effective use of our products.
</li><li>Partners with Regulatory to contribute and partnering to implement regulatory strategies to obtain timely product approvals form worldwide regulatory bodies.
</li><li>Develop the Healthcare Professional (HCPs) and Key Opinion Leaders network and lead a strategic partnership and engagement.
</li><li>Develops and maintains a deep knowledge and understanding of the science behind our products and is seen as an internal expert. To also act as a Speaker in scientific meetings as the voice of the company.
</li><li>Responsible for the governance and compliance within the region. Ensures that all activities are executed as per the Medtronic Business Code of Conduct and local laws and regulations.
</li><li>Utilizes advanced subject matter expertise to provide medical input to various functions (General Management, Global Strategy &amp; Portfolio Management, Business Development &amp; Licensing, Research &amp; Development, &amp; Marketing) and Organizational Units to facilitate insightful decision-making and enable achievement of business objectives.
</li><li>Ensures effective objective value propositions are developed and articulated for Medtronic technologies to stakeholders (patients, health care providers, payers, government agencies, health technology assessment organizations, public) through appropriate channels.
</li><li>Responsible to interpret clinical trials/research, establishes and approves scientific methods for design and implementation of clinical protocols, and final reports.
</li><li>Proactively develops current competitive intelligence in our product space.
</li><li>Represents Medtronic from Clinical Research and Medical Sciences perspective within the region and collects feedback from local customers and authorities.
</li><li>Builds and maintains a strong network and close relationship with the various internal and external parties
</li></ul>Qualifications/ must have
<ul><li>10 years of relevant experience within clinical research &amp; medical sciences with 7+ years of managerial experience, or advanced degree with a minimum of 8 years of relevant experience with 7+ years of managerial experience.
</li><li>University degree &ndash; medical or scientific discipline.
</li><li>Proven strategic thinking, stakeholder management, and team leadership.
</li><li>Fluent in English and local language.
</li><li>Strong communication and networking skills.
</li></ul>Nice to have
<ul><li>Experience in international and cross-functional environments preferred
</li></ul>To be successful in this role you must be an excellent communicator, able to drive change by influence (internally as well as externally) and have strong managerial skills/experience.
Physical Job Requirements
 
 
The above statements are intended to describe the general nature and level of work being performed by employees assigned to this position, but they are not an exhaustive list of all the required responsibilities and skills of this position.
<h1 class="jobSectionHeader">Benefits &amp; Compensation
</h1>Medtronic offers a competitive Salary and flexible Benefits Package
 
A commitment to our employees lives at the core of our values. We recognize their contributions. They share in the success they help to create. We offer a wide range of benefits, resources, and competitive compensation plans designed to support you at every career and life stage. 
 
This position is eligible for a short-term incentive called the Medtronic Incentive Plan (MIP).
This position is eligible for an annual long-term incentive plan.
<h1 class="jobSectionHeader">About Medtronic
</h1>We lead global healthcare technology and boldly attack the most challenging health problems facing humanity by searching out and finding solutions.
 
Our Mission &mdash; to alleviate pain, restore health, and extend life &mdash; unites a global team of 95,000+ passionate people.
 
We are engineers at heart&mdash; putting ambitious ideas to work to generate real solutions for real people. From the R&amp;D lab, to the factory floor, to the conference room, every one of us experiments, creates, builds, improves and solves. We have the talent, diverse perspectives, and guts to engineer the extraordinary.</div>

TuRMECA Clinical Research and Medical Science Director

Kale Grubu

<div>
 
 We are looking for an Associate/Senior Associate to join the Investments and Business Development department of Kale Group.
 
 
 
 
 
 
 Qualifications:
 
 
 
 
 
 
 The following qualifications are required:
 
 <ul>
 <li>
 A strong academic record from a well-recognized institution, having a degree from an engineering or a business school,
 </li>
 <li>
 2 &ndash; 5 years of experience in either management consulting, investment banking, Big4 transaction services &amp; valuation, or corporate development function,
 </li>
 <li>
 Analytical thinking, strong business planning and problem-solving skills,
 </li>
 <li>
 Good understanding of financial modelling and/or finance and accounting knowledge,
 </li>
 <li>
 Ability to work independently with minimal supervision,
 </li>
 <li>
 Familiar with project based working structure, ability to deliver multiple priorities in line with project time plan,
 </li>
 <li>
 Effective verbal, written and interpersonal communication skills.
 </li>
 </ul>
 
 
 
 
 
 
 
 
 
 Responsibilities:
 
 
 
 
 
 
 The successful candidate will have the following responsibilities:
 
 <ul>
 <li>
 Supporting overall portfolio analysis and strategic planning activities,
 </li>
 <li>
 Supporting valuation and feasibility studies, preparation of financial models,
 </li>
 <li>
 Involvement in end-to-end investment and divestitures, acting from both a strategic and financial investor perspectives,
 </li>
 <li>
 Participation in due-diligence projects with end-to-end responsibility on independent work streams,
 </li>
 <li>
 Performing market research studies to identify new business opportunities,
 </li>
 <li>
 Following global and industry related trends to develop company-specific strategies and action plans.
 </li>
 </ul>
 
 
 
 
 
 
 
 Your personal data collected in your applications based on this announcement will be transferred to the data controller Kale Holding A.&Scedil;. ("Kale") will be processed automatically for the purpose of carrying out job application processes within the scope of the Personal Data Protection Law No. 6698 (KVKK) and relevant legislation.
 
 
 You can access the clarification text from the link below.
 
 
 https://www.kalegrubu.com.tr/Uploads/c0045e01945c4c55a215a84ec8ba7f05.pdf
 
</div>

Investments and Business Development Associate/Senior Associate

<div>Start-Up Specialist (Contract Negotiator) 
 Location: office based, Istambul or home based
Join our mission to advance clinical research. 
We&rsquo;re seeking a Site-Readiness and Start-Up Specialist to be the go-to expert for site agreements negotiation with sites in Turkey.
What You&rsquo;ll Do:<ul><li>
Perform initial and amended contract and budget negotiations with the sites</li><li>
Serve as the primary contact for investigative sites during start-up and maintenance</li><li>
Prepare and manage essential regulatory documents for submissions</li><li>
Track timelines, flag risks, and support the team with regulatory expertise</li><li>
Act as a knowledge resource to train or mentor junior colleagues, when applicable</li></ul>
What You Bring:<ul><li>
At least 1 year of experience with contract negotiation</li><li>
Good knowledge of local procedures (submissions and communication via site portals)</li><li>
Good knowledge of MOH tariffs and their implementation in the site budgets</li><li>
Degree in life sciences or equivalent experience.</li><li>
Strong organizational skills, attention to detail, and proactive problem-solving</li><li>
Proficient English language skills</li></ul>
Nice to Have:<ul><li>
Experience with Turkish MOH regulatory systems and sites portals</li></ul>
Why Join Us?
You&rsquo;ll be part of a dedicated, collaborative team driving impactful clinical studies. We offer a flexible work environment, continuous learning, and opportunities to grow within global trials.
Apply now to make a real difference in the future of health!
Learn more about our EEO &amp; Accommodations request here.</div>

Start-up Specialist - Contract negotiation

Explore 291+ Clinical research associate in Istanbul this November. Find roles across top companies and apply now to boost your career.