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2026 financial analyst intern

clinical research intern

Eli Lilly

<div><p>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.</p><p></p><p>
Intern &ndash; Investigator Engagement Assistant (Clinical Research)</p><p>
Purpose:</p><p>
The Intern &ndash; Investigator Engagement Assistant supports the Clinical Research Lead (CRL) and the Investigator Engagement organization in administrative and operational tasks related to clinical trials. This role is designed to provide learning opportunities and entry-level experience in the clinical phase of drug development.</p><p>
Primary Responsibilities: This job description is intended to provide a general overview of the job requirements at the time it was prepared. The job requirements of any position may change over time and may include additional responsibilities not specifically described in the job description. Consult with your supervision regarding your actual job responsibilities and any related duties that may be required for the position.</p><p></p><p><b>
The following are key responsibilities</b></p><p></p><ul><li>
Support office Management (logistics associated with office organisations, supplies)</li><li>
Administrative support for clinical trials as required</li><li>
Assist with document management &ndash; (eg: scan, upload, electronic Trial Master File maintenance activities)</li><li>
In-house administrative support for CRLs who are travelling (eg: confidentiality agreement creation/follow-up, archival of CV, Contract, Ethics committee decisions, invoices, budget forms, proformas)</li><li>
Support Investigator Engagement business systems and process as required</li><li>
Support of local printing and shipment of documents where necessary</li><li>
Support scanning financial documantation and following process</li><li>
Maintenance of collaboration sites</li><li>
Gain working knowledge of local regulatory agency and ethical review board processes</li><li>
Training and working within the boundaries of Good Clinical Practice requirements</li><li>
Working with Good Documentation Practices</li></ul><p>
SIP Support for Investigator Engagement in Turkey:</p><ul><li>
Register site and users by contacting and supporting sites</li><li>
Follow up site profile and facility profile completion</li></ul><p>
Minimum Qualification Requirements:</p><ul><li>
Currently enrolled in a relevant university program (e.g., Life Sciences, Pharmacy, Medicine, or related field).</li><li>
Knowledge of Good Documentation Practices</li><li>
Excellent computer skills with experience in a variety of software packages</li><li>
Fluency in English both written and oral.</li><li>
High level of attention to detail</li><li>
Strong self-management, communication and organizational skills</li></ul><p>
Other Information/Additional Preferences:</p><ul><li>
Flexibility</li><li>
Excellent problem solving skills</li><li>
Ability to work in a virtual team and across cultures</li></ul><p></p><p>
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.</p><p></p><p>
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.</p><p></p>
#WeAreLilly</div>

Clinical Research Intern

Johnson & Johnson

<div><p>At Johnson &amp; Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com</p><p><b>
Job Function:
</b></p>Career Programs<p><b>
Job Sub Function:
</b></p>Non-LDP Intern/Co-Op<p><b>
Job Category:</b></p>
Career Program<p><b>
All Job Posting Locations:</b></p>
Istanbul, Turkey<p><b>
Job Description:</b></p><div><p>
At Johnson &amp; Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com</p></div><div></div><p>
The internship is opened to University students regularly enrolled in the last year of a University course or in their MSc thesis. The internship is 6-months long.</p><p>
The Clinical Operations intern will support daily documentation activities and quality-related activities for the elements applicable to clinical research, from study start-up phase to study closure.</p><p><b>
Activities:</b></p><ul><li>Support Good Documentation Practices.</li><li>Support administrative and logistical support to Local Trial Manager (LTM) and/or Site Manager (SM) in tracking progress of the trial.</li><li>Support ensuring current versions of the required trial documents, trial-relatedmaterials and supplies are provided to the investigational site within requiredtimeframes, as applicable.</li><li>Support Ethics Committee and Health Authority submissions of necessary documentsand follow up the approval.</li><li>Support maintaining information in relevant systems according to the guidelines.</li><li>Support document filing activities by keeping up with timely filing requirements.</li><li>Support for quality complaint process.</li><li>Maintain good understanding of SOPs and local regulations.</li><li>Comply with all training requirements.</li></ul><p><b>
General Activities</b></p><ul><li>Base all actions on Credo. Protect the rights of others, protect privacy and company assets.</li><li>Work in line with the HCC, company policies and procedures, including SOPs, having the ethical aspect in mind. Comply with ICH-GCP and all applicable local laws and regulations.</li><li>Maintain communication with relevant parties within and outside the company</li><li>Actively follow trainings to ensure adequate qualification</li><li>Regularly update information in applicable systems and templates</li><li>Contribute to maintain quality standards and timelines that are consistent with business needs</li><li>Support activities linked to the reporting of J&amp;J</li></ul><p><b>
Requirements:</b></p><ul><li>Students in Biology / Chemistry / Pharmacy / Molecular Biology &amp; Genetics /Bioengineering or related disciplines</li><li>Full competency in local languages and advance level of English</li><li>Organized, and able to work with people within a company environment and musthave strong communication skills</li><li>Demonstrate high discipline, focus, and analytical thinking</li><li>Skilled in Microsoft Office program use.</li></ul><p><b>
Required Skills:
</b></p><p><b>Preferred Skills:</b></p></div>

Clinical Operations Intern

IQVIA

<div>
 The IQVIA Cardiovascular Center of Excellence, a hub of Cardiovascular clinical innovation, is looking for exceptional Board-Certified cardiologist to join our team as a Medical Strategy Lead to help us expand our Cardiovascular portfolio and advance this dynamic and rapidly expanding area of clinical development.
 <br/>
 <br/>
 The Cardiovascular Medical Strategy Lead is a subject matter expert with experience in clinical research and clinical trials who will be a champion for Cardiovascular across IQVIA.
 <br/>
 <br/>
 The key remit of the role is drive growth of the IQVIA Cardiovascular portfolio through scientific and clinical expertise. The Medical Strategy Lead will be charged with using his/her clinical, scientific, and operational knowledge to harness the vast IQVIA data and clinical trial resources to develop innovative, data-driven, and patient-centered solutions for Cardiovascular trials.
 <br/>
 <br/>
 The Medical Strategy Lead will provide senior clinical and scientific expertise to all IQVIA divisions as requested and will collaborate closely with indication-specific teams to develop integrated strategies for Cardiovascular clinical trials, mostly Phases 1-3. The Medical Strategy Lead will also be responsible for early engagement business development activities, providing scientific knowledge and expertise to guide sponsors in Cardiovascular development.
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 <br/>
 As a subject matter expert, the Medical Strategy Lead will drive thought leadership activities including presentations, publications, and interactions with the medical scientific community.
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 <strong>
  Responsibilities
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Accountable and responsible for creating innovative, evidence-based, and patient-centered delivery strategies and solutions for Cardiovascular pre-approval clinical trials or studies, addressing the specific needs and challenges of each customer.
  </li>
  <li>
   In partnership with Indication-Specific Medical Strategy, Operations, Sales, and other functions, responsible for award of strategic and tactical new business to achieve annual Gross New Business targets. Responsible for the inclusion of Cardiovascular elements into proposals.
  </li>
  <li>
   Provide scientific, clinical, and operational advice to internal stakeholders developing proposals: this may include, but is not limited to, providing the strategy to protocol design/clinical development plan, mining data to address important clinical questions relevant to the study, reviewing the protocol for scientific/regulatory soundness and feasibility, identification of target site and principal investigator profiles, anticipated patient recruitment, standard of care and competitive landscape.
  </li>
  <li>
   Support preparation of customer and bid defense meetings, e.g. training and preparation of the assigned project team; provide specific content; ensure presentation focus and content effectively conveys Cardiovascular strategy. Attends and presents at customer meeting, or bid defense or partnership meetings, as required.
  </li>
  <li>
   Participates in strategic business development activities including presentations to prospective clients and professional meetings.
  </li>
  <li>
   Maintains awareness of industry pipeline and scientific and business landscape; supports due diligence research of the Cardiovascular landscape.
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Requirements
  <br/>
  <br/>
 </strong>
 <em>
  Scientific and Research Qualifications and Experience
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  <br/>
 </em>
 <ul>
  <li>
   Cardiologist. A degree from an accredited and internationally recognized school is required
  </li>
  <li>
   2+ years clinical research relevant experience, including hands on operational delivery and/or drug development experience
  </li>
  <li>
   Robust and current knowledge of scientific, clinical, regulatory, commercial and competitive landscape in Cardiovascular
  </li>
  <li>
   Excellent skills in providing consultation and advice on multiple assignments are required, as well as initiative and flexibility.
  </li>
  <li>
   In depth knowledge of, and skill in applying, applicable clinical research regulatory requirements; e.g. Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines
  </li>
  <li>
   Demonstrated ability to understand customer needs, have difficult conversations with internal/external stakeholders and customers, negotiate solutions and understand impacts on the overall offering
  </li>
  <li>
   Strong clinical research skills and commitment to evidence-based and patient-centered clinical development
   <br/>
   <br/>
  </li>
 </ul>
 <em>
  Professional Skills
  <br/>
  <br/>
 </em>
 <ul>
  <li>
   Excellent communication, presentation and interpersonal skills, including good command of English language (both written and spoken)
  </li>
  <li>
   Strong leadership skills, ability to work with minimal supervision, and lead a virtual team in a matrix organization
  </li>
  <li>
   Innovative and strategic thinker
  </li>
  <li>
   Strong business acumen including confidence with financial considerations, excellent negotiation and influencing skills, and comfort working in both sales and operational environments
  </li>
  <li>
   Flexible and able to work in situations where specifications may or may not be well defined and willing to support work in other therapeutic areas when required
  </li>
  <li>
   Confident and capable in the use of technology, applications and other media e.g. databases and internet to research assess new opportunities, maintain currency of therapeutic and operational knowledge and competitive landscape.
  </li>
  <li>
   Proven ability to make decisions with limited information, bringing clarity to disparate information to inform actions and drive results
   <br/>
   <br/>
  </li>
 </ul>
 <em>
  Interpersonal Skills
  <br/>
  <br/>
 </em>
 <ul>
  <li>
   Ability to establish and maintain effective working relationships with co-workers, managers and clients. Maintains a positive outlook at work; handles criticism well and learns from it
  </li>
  <li>
   Ability to establish and maintain effective working relationships with a wide network of individuals e.g. co-workers, managers and customers
  </li>
  <li>
   Effective mentoring and training skills, fostering learning and knowledge sharing with colleagues
   <br/>
   <br/>
  </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 Director, Medical Strategy Lead- Cardiologist

Biçer Güner Attorneys-at-Law

<div>
 <p>
  <strong>
   Join Our Team as a Legal Intern This Summer!
  </strong>
 </p>
 <p>
  <br/>
 </p>
 <p>
  <strong>
   About Us:
  </strong>
 </p>
 <p>
  <br/>
 </p>
 <p>
  <span>
   Bi&ccedil;er G&uuml;ner is a full-service, independent law firm based in Istanbul, T&uuml;rkiye, specializing in corporate/mergers &amp; acquisitions, TMT, banking and finance, dispute resolution, employment law, real estate and data protection. With a strong commitment to delivering high-quality legal services, we provide innovative, practical, and commercially focused solutions to our clients. Our firm values integrity, excellence, and continuous learning, offering an exceptional environment for aspiring legal professionals.
  </span>
 </p>
 <p>
  <br/>
 </p>
 <p>
  <strong>
   Position:
  </strong>
  <span>
   Legal Intern (Summer Internship)
  </span>
 </p>
 <p>
  <strong>
   Duration:
  </strong>
  <span>
   June, July, or August
  </span>
 </p>
 <p>
  <strong>
   Location:
  </strong>
  <span>
   &Idot;stanbul, T&uuml;rkiye
  </span>
 </p>
 <p>
  <br/>
 </p>
 <p>
  <strong>
   Responsibilities:
  </strong>
 </p>
 <p>
  <br/>
 </p>
 <ul>
  <li>
   Conducting legal research and analysis.
  </li>
  <li>
   Contributing to the drafting of legal documents, memos, and correspondence under the supervision of relevant associates.
  </li>
  <li>
   Drafting newsletters and legal alerts on legislative and regulatory developments.
  </li>
  <li>
   Organizing case files and client documentation and internal records.
  </li>
  <li>
   Assisting team members with various projects and tasks across different practice areas.
  </li>
 </ul>
 <p>
  <br/>
 </p>
 <p>
  <strong>
   Qualifications:
  </strong>
 </p>
 <p>
  <br/>
 </p>
 <ul>
  <li>
   Currently enrolled in the second or third year of a reputable law school with strong academic credentials.
  </li>
  <li>
   Proficiency in MS Office.
  </li>
  <li>
   Demonstrated can-do attitude with strong organizational, time-management, follow-up skills.
  </li>
  <li>
   Strong verbal and written skills in both Turkish and English (a valid IELTS and/or TOEFL score will be a plus).
  </li>
  <li>
   Good analytical and communication skills.
  </li>
  <li>
   Ability to perform in-depth legal research with curiosity and attention to detail.
  </li>
  <li>
   Team player with self-motivation, diligence, and a constructive and critical mindset.
  </li>
 </ul>
 <p>
  <br/>
 </p>
 <p>
  <strong>
   How to Apply:
  </strong>
 </p>
 <p>
  <br/>
 </p>
 <p>
  <span>
   If you are ready to take on a challenging and rewarding summer legal internship experience, please submit your resume and a cover letter highlighting your qualifications by 13 February 2026. In your cover letter, please explain why you are interested in this internship and how your skills, academic background, and experience make you a strong candidate for the position.
  </span>
 </p>
 <p>
  <br/>
 </p>
 <p>
  <span>
   Your personal data collected through internship applications will be processed by Bi&ccedil;er G&uuml;ner Attorneys-at-Law, acting as the data controller, by automated means solely for the purposes of carrying out recruitment and job application processes, in accordance with the Personal Data Protection Law No. 6698 and related legislation. You may access more detailed information about your processed personal data and your rights and application methods through:
  </span>
  https://bicerguner.com//userfiles/file/AydinlatmaMetniTR.pdf
  <span>
   .
  </span>
 </p>
</div>


Summer Legal Intern

<div><div><div>Istanbul, T&uuml;rkiye | Full time | Home-based | R1522619</div></div><p></p><div><div><br>
Clinical Trial Educators (CTEs) collaborate with research staff and other stakeholders to drive trial recruitment and support study-specific training needs. The CTE acts as a strategic partner to both external and internal stakeholders to optimize the site experience and performance. They lead relationship management and communication of medical and scientific information with healthcare providers and caregivers. <b>This is a fixed-term opportunity for 12-months contract.</b></div><h3 class="jobSectionHeader"><b>
Essential Functions</b></h3><ul><li><div>
Works with research sites to develop study-specific action plans to accelerate recruitment or support study-specific procedure training</div></li><li><div>
Provides education to healthcare professionals and their staff, reinforcing study protocols as related to a clinical trial</div></li><li><div>
May partner with referral networks to identify potential subjects for a trial</div></li><li><div>
Maintains and analyzes customer records to customize strategies to maximize pre-screening, screening, and enrollment in trials</div></li><li><div>
Completes internal electronic reporting systems; organizes and holds group events to optimize program delivery</div></li><li><div>
Successfully manages objections raised</div></li><li><div>
Maintains up-to-date technical knowledge of specialty and disease areas</div></li></ul><h3 class="jobSectionHeader"><b>
Qualifications</b></h3><ul><li><div>
Bachelor's Degree (BA/BS) in Health Sciences or related field, or equivalent academic/professional qualifications</div></li><li><div>
Registered Nurse or CRA experience is required</div></li><li><div>
1&ndash;2 years of prior relevant experience</div></li><li><div>
High flexibility to travel (internationally, if needed)</div></li><li><div>
Clinical competence in relevant therapeutic area</div></li><li><div>
Excellent interpersonal and communication skills</div></li><li><div>
Strong written and verbal communication skills, including good command of English</div></li><li><div>
Ability to execute tasks with minimal oversight</div></li><li><div>
Ability to coordinate and complete activities across multiple functions</div></li><li><div>
Solutions-based approach to problem-solving</div></li><li><div>
Positive, can-do attitude</div></li><li><div>
Strong customer service orientation</div></li><li><div>
Collaborative mindset and team player</div></li><li><div>
Demonstrates empathy and awareness of cultural differences</div></li><li><div>
Upholds the values of IQVIA and the CTE group</div></li></ul><div>
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></div></div><div></div>

Clinical Trial Educator

<div>
 Clinical Trial Educators (CTEs) collaborate with research staff and other stakeholders to drive trial recruitment and support study-specific training needs. The CTE acts as a strategic partner to both external and internal stakeholders to optimize the site experience and performance. They lead relationship management and communication of medical and scientific information with healthcare providers and caregivers.
 <strong>
  This is a fixed-term opportunity for 12-months contract.
  <br/>
  <br/>
 </strong>
 <strong>
  Essential Functions
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Works with research sites to develop study-specific action plans to accelerate recruitment or support study-specific procedure training
  </li>
  <li>
   Provides education to healthcare professionals and their staff, reinforcing study protocols as related to a clinical trial
  </li>
  <li>
   May partner with referral networks to identify potential subjects for a trial
  </li>
  <li>
   Maintains and analyzes customer records to customize strategies to maximize pre-screening, screening, and enrollment in trials
  </li>
  <li>
   Completes internal electronic reporting systems; organizes and holds group events to optimize program delivery
  </li>
  <li>
   Successfully manages objections raised
  </li>
  <li>
   Maintains up-to-date technical knowledge of specialty and disease areas
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Qualifications
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Bachelor's Degree (BA/BS) in Health Sciences or related field, or equivalent academic/professional qualifications
  </li>
  <li>
   Registered Nurse or CRA experience is required
  </li>
  <li>
   1&ndash;2 years of prior relevant experience
  </li>
  <li>
   High flexibility to travel (internationally, if needed)
  </li>
  <li>
   Clinical competence in relevant therapeutic area
  </li>
  <li>
   Excellent interpersonal and communication skills
  </li>
  <li>
   Strong written and verbal communication skills, including good command of English
  </li>
  <li>
   Ability to execute tasks with minimal oversight
  </li>
  <li>
   Ability to coordinate and complete activities across multiple functions
  </li>
  <li>
   Solutions-based approach to problem-solving
  </li>
  <li>
   Positive, can-do attitude
  </li>
  <li>
   Strong customer service orientation
  </li>
  <li>
   Collaborative mindset and team player
  </li>
  <li>
   Demonstrates empathy and awareness of cultural differences
  </li>
  <li>
   Upholds the values of IQVIA and the CTE group
   <br/>
   <br/>
  </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>


AbbVie

<div><b>Company Description</b><p><br>
AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas &ndash; immunology, oncology, neuroscience, and eye care &ndash; and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on X, Facebook, Instagram, YouTube, LinkedIn and Tik Tok.</p><b><br>
Job Description</b><p><br>
Ensure medical compliance while aligning with international and domestic business development strategies.</p><ul><li>
Identify opportunities and medical needs/ requests propose strategies and manage execution of agreed strategic medical projects linked with brand strategies.</li><li>
Cooperate with clinical research team to provide appropriate clinical input regarding the therapeutic area and jointly work in identifying and contacting potential sites and investigators.</li><li>
Provide response to questions and requests for medical information from the Medical Community and the sales team, based on practical and theoretical knowledge, utilizing all available resources where appropriate, including pharmacovigilance issues.</li><li>
For medical related issues, jointly work within brand team in preparation and participation in scientific meetings and events.</li><li>
To support Brand Managers in preparing promotional material and review it to ensure the highest level of clinical and scientific accuracy. Provide scientific &amp; medical expertise to support the related brand team and contribute proactively to the successful implementation of brand plans.</li><li>
Provide medical trainings to internal &amp; external partners (ie speaker briefings).</li><li>
Build long-term relationships with identified KOLs, to achieve medical objectives through regular and continuous external engagements.</li></ul><br>
<b>
Qualifications</b><br>
<ul><li>
University degree in Medicine or Pharmacy,</li><li>
Minimum 1 year experience as Medical Science Liaison or Medical Manager,</li><li>
Fluency in English,</li><li>
Experience in developing and maintaining expert knowledge for the assigned therapeutic area, and in medical research in general,</li><li>
Solid knowledge of the pharmaceutical environment and the role of medical affairs to advance the medical and scientific objectives of a pharmaceutical company,</li><li>
Demonstrated expertise in the scientific methods applied to clinical research and current legislative/regulatory controls applicable to this research.</li></ul><br>
<b>
Additional Information</b><div></div><p><br>
AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled.</p><p>
US &amp; Puerto Rico only - to learn more, visit https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html</p><p>
US &amp; Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:</p><p>
https://www.abbvie.com/join-us/reasonable-accommodations.html</p></div>

Medical Manager, Immunology

Explore 151+ Clinical research intern in Istanbul this January. Find roles across top companies and apply now to boost your career.

151 clinical research intern jobs IN Istanbul

Clinical Research Intern

Clinical Operations Intern

Senior Director, Medical Strategy Lead- Cardiologist

Summer Legal Intern

Clinical Trial Educator

Clinical Trial Educator

Medical Manager, Immunology