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clinical research lead

Eli Lilly

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

Clinical Research Lead

Fortrea

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

Clinical Project Manager sponsor-dedicated

IQVIA

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

Senior Business Systems Analyst/Product Owner

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>Atrial fibrillation affects over 33 million individuals worldwide and is the most common form of serious arrhythmia. Being in a fast-growing cardiac ablation business segment and with recent acquisition of the AFFERA&trade; Mapping and Ablation System, we are poised to provide innovative solutions to address unmet needs for many patients. We are seeking a talented and motivated Senior AFFERA&trade; Therapy Account Consultant to join our team to further drive the growth of the business.
 
Reporting the operating unit this role is critical in providing expert clinical and technical support and training to physicians and EP Lab Staff on the optimal use of the AFFERA&trade; Mapping and Ablation System.
Responsibilities may include the following and other duties may be assigned:
<ul><li>Provide proficient clinical and technical assistance to physicians and EP Lab Staff on the use of the Affera&trade;&#65039; Mapping and Ablation System and related equipment (Generators, SW functionalities, pump and accessories).
</li><li>Serve as technical adviser/expert, demonstrating products/service, providing T&amp;E, in-service or trade show support and troubleshooting product issues.
</li><li>Adapt and contribute to short and long-range plans, goals, and objectives for the Affera&trade; Mapping and Ablation System. Adapt and deploy product / service value proposition.
</li><li>Conduct competitive product analysis, opportunity assessment and market research.
</li><li>Be an active participant to the development of advanced clinical workflows.
</li><li>Work closely with the education team and support the development of training centers.
</li><li>Stay abreast of all products information across the Medtronic CAS portfolio, instructions for use (IFU) and relevant scientific clinical literature and new product information.
</li><li>Be responsible for product launch strategies for new site activation as well as ensuring effective product placement relative to customer needs.
</li></ul>Required Knowledge and Experience:
<ul><li>Bachelor's degree required in electrical or medical engineering or related scientific disciplines or equivalent experience.
</li><li>3+ years of clinical EP experience.
</li><li>Minimum of 2 years of successful independent support of EP mapping procedures.
</li><li>IBHRE or equivalent certification is a plus.
</li><li>Fluency in English, any other European languages are advantageous.
</li><li>Valid driving license
</li><li>Ability to manage high-stress situations with a clear problem-solving mindset.
</li><li>Ability to ensure knowledge transfer to other colleagues and peers when requested.
</li><li>Ability to maintain a high level of responsiveness to customer or other internal and external stakeholders.
</li></ul>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. 
 
<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>

Senior Affera Mapper

Amgen

<div>Join Amgen&rsquo;s Mission of Serving Patients
At Amgen, if you feel like you&rsquo;re part of something bigger, it&rsquo;s because you are. Our shared mission&mdash;to serve patients living with serious illnesses&mdash;drives all that we do.
Since 1980, we&rsquo;ve helped pioneer the world of biotech in our fight against the world&rsquo;s toughest diseases. With our focus on four therapeutic areas &ndash;Oncology, Inflammation, General Medicine, and Rare Disease&ndash; we reach millions of patients each year. As a member of the Amgen team, you&rsquo;ll help make a lasting impact on the lives of patients as we research, manufacture, and deliver innovative medicines to help people live longer, fuller happier lives.
Our award-winning culture is collaborative, innovative, and science based. If you have a passion for challenges and the opportunities that lay within them, you&rsquo;ll thrive as part of the Amgen team. Join us and transform the lives of patients while transforming your career.
Live
What you will do
Let&rsquo;s do this! Let&rsquo;s change the world! The role provides proactive end to end quality support for the development and implementation of a risk-based quality assurance strategy for the clinical development program.
The role will support end to end quality oversight of the General Medicine &amp; Obesity Therapeutic Area and will be responsible for supporting a risk-based quality strategy that advances quality by design principles for the full clinical trial lifecycle (protocol development, database lock, and regulatory submissions/ approvals).
You will play a vital role by developing deep knowledge of the clinical trials you support and provide oversight and quality management of critical data and processes for global and local study teams and all clinical trial sites who participate in Amgen sponsored trials.
Responsibilities<ul><li>
Act as a Good Clinical Practice (GCP) Subject Matter Expert, offering independent, objective quality guidance.</li><li>
Oversee quality across all clinical development stages.</li><li>
Plan and execute risk-based GCP audits (sites, affiliates, vendors, studies).</li><li>
Support regulatory inspections and guide responses, including root cause analysis and CAPAs.</li><li>
Lead quality oversight of Risk Assessment Categorization Tools (RACT) for each trial.</li><li>
Facilitate monthly quality risk reviews with clinical program leaders.</li><li>
Manage audit findings, deviations, and CAPA responses.</li><li>
Ensure regional compliance with local regulations and support vendor evaluations.</li><li>
Analyze data quality trends, identify gaps, and implement corrective actions.</li><li>
Oversee technologies for endpoint data collection (e.g., biomarkers, imaging).</li><li>
Develop and execute TA-specific QA plans and protocol-specific audit strategies.</li><li>
Support quality management activities including deviations, breaches, and inspection readiness.</li><li>
Drive innovation in quality oversight using data analytics, AI, and NLP.</li><li>
Review protocols to simplify design and identify critical data/processes.</li></ul>
Country/ Regional Quality Leadership<ul><li>
Manage analytical tools and data trends to address site/regional quality gaps.</li><li>
Provide oversight for key sites in collaboration with regional operations.</li><li>
Conduct Quality Partnership Visit at key sites within the country/Region</li><li>
Share best practices and compliance insights with stakeholders.</li><li>
Offer independent quality consultation and escalate issues as needed.</li><li>
Support local vendor assessments and pre-inspection activities.</li><li>
Conduct regional risk assessments for audit planning.</li><li>
Stay current on regulatory trends and deliver ongoing training.</li></ul>
Win
WHAT WE EXPECT OF YOU
We are all different, yet we all use our unique contributions to serve patients. The individual we seek has technological literacy and leadership skills, and has these qualifications:
Doctorate degree and 2 years of Quality Management, Quality Assurance and Good Clinical Practices experience in the pharmaceutical/biotech industry where risk-based quality management and quality by design are a core responsibility.
Or
Master&rsquo;s degree and 4 years of the previous mentioned experience
Or
Bachelor&rsquo;s degree and 6 years of the previous mentioned experience
Or
Associate&rsquo;s degree and 10 years of the previous mentioned experience<ul><li>
Oversight and implementation of Quality Management Systems and experience managing quality in electronic QMS such as Veeva or Track wise.</li><li>
Thorough understanding of Clinical R&amp;D activities and Global Regulations.</li><li>
Experience with Regulatory Submission and Inspection Management procedures.</li><li>
Quality Oversight of Clinical Trials, including clinical trial protocol development, execution, and submissions.</li><li>
Leadership or mentoring experience is ideal, in a regional capacity would be phenomenal.</li><li>
Excellent verbal and written communication skills, including strong business writing abilities and active listening. Able to understand and articulate technical concepts and literature in spoken and written English.</li><li>
Ability to transform business and stakeholder feedback into clear, efficient processes using a straightforward language and format.</li><li>
Self-driven with strong analytical, critical-thinking, prioritization, and decision-making abilities.</li></ul><h2 class="jobSectionHeader">
IMPORTANT! Please submit your resume/CV in English!</h2><h2 class="jobSectionHeader">
Thrive</h2>
WHAT YOU CAN EXPECT OF US<ul><li>
Vast opportunities to learn, develop, and move up and across our global organization.</li><li>
Diverse and inclusive community of belonging, where colleagues are empowered to bring ideas to the table, take risks, and act.</li><li>
Generous Amgen Total Rewards Plan comprising healthcare, finance, wealth and career benefits.</li><li>
Flexible work arrangements.</li></ul><h2 class="jobSectionHeader">
Apply now</h2>
In our quest to serve patients above all else, Amgen is the first to imagine, and the last to doubt. Join us: Careers.amgen.com
As an organization dedicated to improving the quality of life for people around the world, Amgen fosters an inclusive environment of diverse, ethical, committed and highly accomplished people who respect each other and live the Amgen values to continue advancing science to serve patients. Together, we compete in the fight against serious disease.
Amgen is an Equal Opportunity employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability status, or any other basis protected by applicable law.
We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation.</div>

Quality Compliance Senior Manager

MicroPort

<div>
 
 As a Technical Engineer for Surgical Robots, you will be responsible for ensuring the optimal performance, maintenance, and support of our robotic surgical systems. The successful candidate will work collaboratively with cross-functional teams to address technical challenges and contribute to the ongoing improvement of our robotic technologies.
 
 
 
 
 **Key Responsibilities:**
 
 
 1. **System Installation and Configuration:**
 
 
 - Lead the installation and configuration of robotic surgical systems in healthcare institutions, ensuring compliance with technical specifications and guidelines.
 
 
 - Provide technical expertise during the setup process to optimize system performance.
 
 
 
 
 2. **Troubleshooting and Technical Support:**
 
 
 - Diagnose and resolve technical issues related to robotic systems through remote support or on-site intervention.
 
 
 - Collaborate with Clinical team to provide timely and effective solutions to end-users.
 
 
 
 
 3. **Preventive Maintenance:**
 
 
 - Develop and implement preventive maintenance schedules for robotic systems to minimize downtime and ensure continuous functionality.
 
 
 - Conduct routine inspections and updates to prevent potential issues.
 
 
 
 
 4. **Training and Documentation:**
 
 
 - Deliver technical training to healthcare professionals and internal staff on the use and maintenance of robotic surgical systems.
 
 
 - Create and update technical documentation, manuals, and troubleshooting guides.
 
 
 
 
 5. **Collaboration with R&amp;D:**
 
 
 - Work closely with the research and development team to provide insights and feedback from a technical perspective.
 
 
 - Participate in testing and validation of new software and hardware releases.
 
 
 
 
 6. **Quality Assurance:**
 
 
 - Contribute to the development and implementation of quality assurance processes for robotic systems.
 
 
 - Assist in the investigation and resolution of any technical issues related to product quality.
 
 
 
 
 **Qualifications:**
 
 
 - Bachelor&rsquo;s degree in Engineering, Cor a related technical field; advanced degree is a plus.
 
 
 - Proven experience in technical support or engineering roles in the medical device industry.
 
 
 - Familiarity with robotic systems and control systems is highly desirable.
 
 
 - Strong problem-solving and analytical skills.
 
 
 - Excellent communication skills and the ability to collaborate effectively with cross-functional teams.
 
 
 - Willingness to travel for on-site technical support and installations.
 
</div>

Technical Engineer

Exeltis Turkey

<div>
 
 
 Medical Manager
 
 
 
 
 
 
 We are looking for a Medical Manager to be assigned to our Head Office at Exeltis Turkey.
 
 
 
 
 
 
 Qualifications
 
 
 <ul>
 <li>
 Medical Doctor (MD) degree,
 </li>
 <li>
 Excellent command of written and spoken English,
 </li>
 <li>
 Proficient in MS Office applications and effective presentation techniques,
 </li>
 <li>
 Strong sense of responsibility with analytical and strategic thinking skills,
 </li>
 <li>
 Holder of a valid B-class driving license and actively driving,
 </li>
 <li>
 No restrictions on travel.
 </li>
 <li>
 Experience in Respiratory Field will be preferred
 </li>
 </ul>
 
 
 
 
 
 Job Description
 
 
 <ul>
 <li>
 Providing continuous medical update and support for existing products,
 </li>
 <li>
 Represent the company at Scientific Congresses, trainings, and medical meetings,
 </li>
 <li>
 Provide medical support to Marketing and Sales teams during scientific presentations,
 </li>
 <li>
 Contribute medical insights to product strategies,
 </li>
 <li>
 Conduct meetings with key opinion leaders (KOLs) and Health Authorities regarding assigned products,
 </li>
 <li>
 Plan, initiate, and monitor clinical research activities,
 </li>
 <li>
 Oversee pharmacovigilance operations and ensure the pharmacovigilance system remains compliant with current regulatory requirements
 </li>
 </ul>
 
 
</div>

Medical Manager

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