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2026 commercial & investment bank - global corporate banking program- (large-cap) -off-cycle internship- (february-july ) – istanbul Jobs in Istanbul

2026 commercial & investment bank - global corporate banking program- (large-cap) -off-cycle internship- (february-july ) – istanbul

clinical research intern

<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

<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>

IQVIA

<div>Job Overview
The medical department consists of a Chief Medical Officer, Medical Directors, Sr Medical Directors, Medical Writers, and Safety Associates. The Medical Director provides medical and scientific support to clinical research programs, study teams and investigators. The Medical Director also provides review, advice, and leadership for potentially or awarded clinical research programs.
The Medical Director role is a team member participant role and functions in a matrix report to project teams much like other members of the project teams. The primary role of Medical Director is to provide medical oversight for clinical trials by serving as Medical Monitor for studies conducted by IQVIA Biotech Clinical on behalf of sponsor companies. The principal function of a Medical Monitor is to serve as primary contact for the sponsor medical team and to serve as front line medical resource to support the project team. The Medical Monitor is customarily available 24/7 to answer questions from site coordinators and investigators on protocol inclusion/exclusion criteria, protocol clarifications, and compliance issues, and to provide review of alert labs per sponsor preference. Major duties of the Medical Director are outlined below:
Essential Functions
Functions as project team member:
<ul><li>Provides medical and scientific input to clinical research programs including review of new business proposals, preclinical and/or clinical data, study protocols, training materials, informed consent, Investigator Drug Brochures, eCRFs, analysis plan designs, clinical study reports, regulatory approval submissions, serious and non-serious adverse event evaluation, and reporting.
</li><li>Ensures medical activities run according to GCP and operate with highest efficiency.
</li><li>Establishes and maintains a network of medical/scientific consultants, etc.
</li><li>Supervises and manages Medical Director activities.
</li></ul>Clinical Activities:
<ul><li>Interacts with clients regarding drug development programs, study design and protocol.
</li><li>Reviews and provides input for protocol development. Interacts with key thought leaders and/or sponsor representatives to develop inclusion/exclusion criteria and study endpoints.
</li><li>Interacts in team approach to develop statistical and data management sections of the protocol.
</li><li>Reviews the final protocol for clinical, safety and efficacy variables.
</li><li>Provides project team training on protocol and/or therapeutic areas.
</li><li>Assists team with developing criteria for investigator site selection and networking for potential investigators for study participation. Aids in review and final selection.
</li><li>Participates in subject recruitment and retention activities including individual calls to key opinion leaders, investigators, and site staff and/or participation in teleconference and WebEx presentations.
</li><li>Presents protocol and/or safety reporting information at investigator meetings.
</li><li>Develops project medical monitoring plans as requested.
</li><li>Provides on call coverage for protocol queries and site support.
</li><li>Provides first line contact for investigators and monitors regarding study related medical/safety issues and resolution of study protocol and patient eligibility issues.
</li></ul>Safety Monitoring and SAE Reporting Activities:
<ul><li>Verifies the medical accuracy of patient safety data and maintains an ongoing assessment of the safety profile of the study.
</li><li>Provides medical review of SAE reporting, writes and/or reviews SAE narratives, and works with the Safety Management Department to track SAEs and follow-up on outstanding safety queries, interacts with sponsor and discusses safety issues with site as needed.
</li><li>Reviews IND/SUSAR Safety Reports (per sponsor preference), updates to Investigator Brochures, and annual IND reports with sponsor data.
</li><li>In consultation with the sponsor, follow procedures for acquiring knowledge of subject treatment assignments (i.e. breaking the blind).
</li><li>Interact with appropriate FDA officials concerning safety and other study related issues, as requested.
</li></ul>Data Activities:
<ul><li>Provides medical review of eCRFs for clinical accuracy.
</li><li>Provides medical review of data analysis plan.
</li><li>Reviews safety fields at case freeze for reconciliation (if needed).
</li><li>Works with data group to reconcile SAE events as needed.
</li><li>Reviews medical coding of adverse events, laboratory data and concomitant medications for accuracy, coherence, consistency, and trends.
</li><li>Reviews data tables, listings, and figures.
</li><li>Reviews and/or writes portions of final clinical study report.
</li></ul>DSMB/Adjudication Committee Activities:
<ul><li>May assist sponsor in choosing committee members.
</li><li>May serve as a non-voting member to convene and organize proceedings.
</li><li>May develop operating guidelines in conjunction with committee members and submits these to sponsor for review.
</li><li>May determine data flow with sponsor to ensure reporting accuracy.
</li><li>Can ensure DSMB feedback is given to sites for IRBs.
</li><li>All DSMB activities are usually managed by the IQVIA Biotech Oversight Management Group and not the IQVIA Biotech medical monitor.
</li></ul>Business Development Activities:
<ul><li>Work with Business Development to actively solicit new business for Novella Clinical, including assistance with marketing presentations and proposal development.
</li><li>Supports business development activities with proposal development and sales presentations.
</li><li>Participates in feasibility discussions relating to specific project proposals.
</li></ul>Special Projects:
<ul><li>Obtain literature searches to acquire background information for study proposals, preparation of training sessions, and interpretation of clinical data, report writing, etc.
</li><li>Assists with drafting of standard operating procedures and working practices regarding all Medical Director activities.
</li><li>Participate in a variety of team quality improvement efforts as necessary.
</li><li>Perform other related duties as assigned or requested by the Chief Medical Officer.
</li></ul>Qualifications
<ul><li>Medical Degree from an accredited and internationally recognized medical school with a curriculum relevant to general medical education.
</li><li>10 years of experience is required which can include medical practice (hospital/clinic), academia, clinical research, or drug development.
</li><li>3-5 years of biopharmaceutical (industry) experience is preferred which can be part of the 10-year experience.
</li><li>Ability to work in partnership with a multidisciplinary group of colleagues, including translating concepts into practical approaches and promoting consensus.
</li><li>Outstanding ability to work independently with minimal supervision, ability to work effectively within a team, and matrix environment.
</li><li>Ability to organize and work efficiently on several projects, each with specific requirements and/or shifting priorities.
</li><li>Excellent oral and written communications skills as well as interpersonal skills are essential.
</li></ul>Oncology / Hematology
<ul><li>Current or prior license to practice medicine; board certification/eligibility ideal (Preference)
</li><li>Board Certified / Board Eligible: Oncology (Required)
</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>

Medical Director - Oncology , Home- Based

Creatives Data

<div>
 
 We are currently seeking a passionate, creative, and detail-oriented Graphic Design Intern to join our creative team in our production studio. This is an excellent opportunity for recent graduates or senior-year students from Graphic Design, Visual Communication Design, Fine Arts, or related departments who are eager to develop their skills in the professional world of design and branding.
 
 
 
 
 
 About the Role
 
 
 
 
 
 As a Graphic Design Intern, you&rsquo;ll work closely with our branding, marketing, and production teams to create engaging visual content for digital, social, print, and commercial platforms. You&rsquo;ll be part of a collaborative environment where creativity, visual excellence, and strong brand storytelling are essential.
 
 
 
 
 
 🚨
 
 🚨
 
 IMPORTANT NOT&Idot;CE : Applications of candidates who do not share their portfolio, their portfolio link or their portfolio links on platforms such as Behance will not be taken into consideration.
 
 🚨🚨
 
 
 
 
 
 
 
 🚨🚨🚨🚨
 
 Dear intern applicants, a CV and a portfolio are two separate entities. Don't assume that the CV you include in your application is a portfolio. A portfolio is a document that compiles and presents examples of your work, whether during or after your education. You can submit this document directly or through a link you've included in your CV. The first thing we consider when evaluating you is your design work to date. We then proceed to evaluate you based on what's on your CV. We can't evaluate you based on your first and last name, school, photo, or other information. As a graphic design intern, we can evaluate you based on your previous work. Please include links or files where we can access your work.
 
 🚨🚨🚨🚨
 
 
 
 
 
 
 🎯 Key Responsibilities
 
 
 
 
 <ul>
 <li>
 Create visual assets and designs for social media posts, campaigns, digital ads, and print materials
 </li>
 <li>
 Assist in developing brand identities, including logos, color palettes, typography, and visual guidelines
 </li>
 <li>
 Collaborate on the creation of mood boards and visual concepts
 </li>
 <li>
 Edit and prepare graphic content tailored specifically for Instagram, TikTok, and other social platforms
 </li>
 <li>
 Support the design team with layout, image editing, and asset production
 </li>
 <li>
 Participate in brainstorming sessions and propose innovative design ideas
 </li>
 <li>
 Assist in organizing and archiving design files and resources
 </li>
 </ul>
 
 
 
 
 ✅ What We&rsquo;re Looking For
 
 
 
 
 <ul>
 <li>
 University student or recent graduate from Graphic Design, Visual Communication Design, Fine Arts, or related fields
 </li>
 <li>
 Strong proficiency in Adobe Creative Suite (Photoshop, Illustrator, InDesign; knowledge of Adobe XD or Figma is a plus)
 </li>
 <li>
 Basic knowledge of visual hierarchy, typography, color theory, and composition
 </li>
 <li>
 Familiarity with current design trends, especially for social media platforms like Instagram &amp; TikTok
 </li>
 <li>
 A portfolio or collection of past works (student projects are acceptable)
 </li>
 <li>
 Eagerness to learn, take initiative, and actively contribute to the creative process
 </li>
 <li>
 Ability to meet deadlines, manage multiple tasks, and follow creative direction
 </li>
 <li>
 Team player with strong visual instincts and attention to detail
 </li>
 </ul>
 
 
 
 
 ⭐ Bonus Skills
 
 
 
 
 <ul>
 <li>
 Interest or experience in motion graphics or animation (Adobe After Effects)
 </li>
 <li>
 Basic knowledge of photo editing and retouching (Adobe Lightroom)
 </li>
 <li>
 Familiarity with branding processes or previous branding projects
 </li>
 <li>
 Experience with moodboarding, visual research, and style exploration
 </li>
 </ul>
 
 
 
 
 💡 What You&rsquo;ll Gain
 
 
 
 
 <ul>
 <li>
 Real-world experience on diverse, live brand and design projects
 </li>
 <li>
 One-on-one mentorship from experienced graphic designers, art directors, and brand strategists
 </li>
 <li>
 Access to a dynamic, creative, and collaborative work environment
 </li>
 <li>
 Opportunity to grow your professional portfolio with high-quality commercial and brand-focused work
 </li>
 <li>
 Flexible working hours with potential extension to part-time employment
 </li>
 <li>
 Paid internship opportunity
 </li>
 </ul>
</div>

Graphic Designer Intern

<div>Job Overview 
 
Serve as Senior Data Coordinator for allocated complex studies and serve in a leadership role to a specific DM Task.
Essential Functions
<ul><li>Serve as a lead DM and the main point of contact for various projects managed by the team.
</li><li>Ensure that all the deliverables are of expected quality standards and meet customer expectations
</li><li>Attend study kick off meetings and internal/sponsor audits for assigned studies.
</li><li>Report on the quality of data collection and site issues to Data Management Team Leaders and apprise them of the status of each project.
</li><li>Interact with the Clinical Data Management personnel for project timelines, delivery of quality data and frequent project update teleconferences.
</li><li>Ensure that at the end of the study, all the Data Clarification forms are resolved, all data is &ldquo;cleaned&rdquo;, the data transfer is sent to the sponsor as per the agreed specifications, the data and the study files are completed and archived appropriately.
</li><li>Mentor other team members and ensure the completion of all required trainings.
</li><li>Assist in developing and implementing new technology / database revisions.
</li></ul>Qualifications
<ul><li>Bachelor's Degree Clinical, biological or mathematical sciences, or related field
</li><li>Clinical Data Management or Equivalent combination of education, training and experience in lieu of degree.
</li><li>Excellent organizational, communication and computer skills.
</li><li>Ability to exercise excellent attention to detail.
</li><li>Ability to act independently and with initiative required to resolving problems.
</li><li>Knowledge of Computer application- MS Office, Word and Excel
</li><li>Internet usage, Clinical application Programming /Macro knowledge will be helpful.
</li><li>Ability to establish and maintain effective working relationships with coworkers, managers and clients.
</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>

Sr. Clin Data Coordinator

Explore 245+ Clinical research intern in Istanbul this October. Find roles across top companies and apply now to boost your career.

245 clinical research intern jobs IN Istanbul

Clinical Research Intern

Clinical Research Intern

Associate Legal Counsel

Associate Legal Counsel

Medical Director - Oncology , Home- Based

Graphic Designer Intern

Sr. Clin Data Coordinator