Site Name: Field Worker - DEU (Munich) Posted Date: Apr 1 2026 Senior GynOnc Clinical Trial RMAM (m/f/d) The Senior GynOnc Clinical Trial RMAM is responsible for the successful conduction of all our clinical trials in Germany and is responsible for efficient and compliant management of medical and scientific study activities to generate robust evidence that supports the scientific positioning and the medical care of patients. Responsibilities This role will provide YOU the opportunity to lead key activities to progress YOUR career. These responsibilities include some of the following: - Lead and coordinate medical research activities on a local level to ensure high scientific and operational quality - Ensures that all clinical studies are planned, executed and communicated in line with regulatory standards and company objectives - Manage internal and external partners to ensure quality, timelines and budget are met - Develop regional omnichannel engagement plans, combining face-to-face and digital outreach to meet healthcare professional needs. - Acting as a central interface between local and global Medical Affairs stakeholders, regional medical affairs managers, clinical development and clinical research organizations to ensure cross-functional collaboration - Plan and run regional medical activities such as advisory boards, symposia and educational meetings. - Contributes to the generation of high-impact and robust data in clinical trials to inform treatment decisions, support product differentiation and improve outcomes for oncology patients - Mentor and support development of more junior medical colleagues. Basic Qualification - Advanced degree in medicine, pharmacy, life sciences or related field (MD, PharmD, PhD or equivalent). - At least 5 years experience in medical affairs, medical science liaison, clinical research or related industry role. - Strong clinical and scientific knowledge relevant to the therapy area for the role. - Excellent verbal and written communication skills in German and English. - Willingness and ability to travel regularly within the assigned region. - Solid understanding of regulatory, ethical and compliance requirements in the pharmaceutical environment. Preferred Qualification If you have the following characteristics, it would be a plus: - Prior experience in GynOnc, oncology or related therapy areas. - Experience supporting investigator-initiated trials or clinical partnerships. - Experience designing or delivering omnichannel engagement plans and digital medical communications. - Project management or budget management experience. - Experience presenting at national or regional scientific meetings. - A collaborative mindset and commitment to inclusive working with diverse stakeholders. Weitere Informationen:  Annual Report Product Pipeline #EBDE #LI-ViiV #LI-Remote 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 – to impact health at scale. People and patients around the world count on the medicines and vaccines we make, so we’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. Should you require any adjustments to our process to assist you in demonstrating your strengths and capabilities contact us at DE.Contact-Recruitment@gsk.com where you can also request a call. Please note should your inquiry not relate to adjustments, we will not be able to support you through these channels. However, we have created a Recruitment FAQ guide. Click the link where you will find answers to multiple questions we receive. GSK is an Equal Opportunity Employer. This ensures that all qualified applicants will receive equal consideration for employment without regard to ethnicity, colour, religion, sex (including pregnancy, gender identity, and sexual orientation), parental status, national origin, age, disability, genetic information (including family medical history), military service or any basis prohibited under federal, state or local law. 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. Please note that if you are a US Licensed Healthcare Professional or Healthcare Professional as defined by the laws of the state issuing your license, GSK may be required to capture and report expenses GSK incurs, on your behalf, in the event you are afforded an interview for employment. This capture of applicable transfers of value is necessary to ensure GSK’s compliance to all federal and state US Transparency requirements. For more information, please visit the Centers for Medicare and Medicaid Services (CMS) website at https://openpaymentsdata.cms.gov/

Unit: School of Nursing Department: Research Duties & Responsibilities: Summary: VCU School of Nursing is seeking a Clinical Research Assistant to support the collection of qualitative research data through virtual interviews and participant engagement in an ongoing research project. The Research Assistant will collaborate with the Project Director and research team to coordinate and conduct virtual data collection, primarily through Zoom interviews with patient and family participants as well as healthcare providers. The Research Assistant will play a key role in data collection, participant coordination, and research operations support. Typical Duties - Coordinate recruitment, scheduling, and communication with patient, family, and healthcare provider participants. - Obtain informed consent from participants and explain study procedures prior to interviews. - Schedule and facilitate Zoom interviews with research team for research participants while ensuring a professional and supportive interview environment. - Upload and organize interview recordings, transcripts, and study documents in secure research platforms (e.g., REDCap or shared research drives). - Maintain organized records of recruitment, interview scheduling, and completion of study activities. - Support participant retention by maintaining clear communication, ensuring compensation, and providing follow-up as needed. - Coordinate with the research team to ensure data are properly documented and available for analysis. - Participate in regular research team meetings to provide updates on recruitment and interview progress. - Follow IRB-approved procedures for informed consent, confidentiality, and secure data handling. - Assist with preparation of study reports and documentation related to research progress. - Assist with manuscripts and grant writing as needed. - Assist with coordination of a multi-site, multi-disciplinary study (VCU, University of Iowa, Nest Genomics) - Other duties as assigned. Minimum Qualifications - Bachelor’s degree in a related field, or equivalent training and experience - Experience using Zoom or other virtual meeting platforms - Strong communication and interpersonal skills, particularly when interacting with research participants - Ability to work effectively with patients, families, and healthcare professionals - Excellent organizational skills and attention to detail - Ability to maintain confidentiality and manage sensitive information - Competence with Microsoft Office Suite - Demonstrated experience working in and fostering an environment of respect, professionalism and civility with a population of faculty, staff, and students from all backgrounds and experiences, or a commitment to do so as a staff member at VCU Preferred Qualifications - Experience assisting with qualitative research or interview-based studies - Demonstrated interest or experience in health sciences, genetic counseling, or cardiology - CITI Training in Biomedical or Social Sciences - Experience with research data management platforms (e.g., REDCap) - Experience working in healthcare or academic research settings - Experience coordinating research participants or conducting interviews This is a part-time position with an anticipated end date of September 2026. Position will remain open until filled, with a priority application date of April 8. Hourly Range: $20/hour FLSA Exemption Status: Non-Exempt Hours per Week: 8-12 Contact Information: Contact Name: Bruna Soria Galvarro Contact Email: soriagalvaba@vcu.edu

Clinical Trial Liaison- Poland ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development We are currently seeking a Clinical Trial Enrollment Liaison to join our diverse and dynamic team. As a Clinical Trial Enrollment Liaison at ICON, you will play a pivotal role in designing and analyzing clinical trials, interpreting complex medical data, and contributing to the advancement of innovative treatments and therapies. What you will be doing - Collaborate with cross-functional teams to design and implement effective clinical trial enrollment strategies. - Analyze and interpret clinical trial data, ensuring accuracy and compliance with regulatory standards. - Foster strong relationships with study sites and investigators to enhance patient recruitment and retention. - Act as a liaison between sponsors, investigators, and study participants, providing support and guidance throughout the enrollment process. - Contribute to the continuous improvement of enrollment processes and strategies to optimize trial outcomes. Your profile - Bachelor's degree in a relevant field, such as life sciences or healthcare. - Proven experience in clinical trial enrollment or related roles. - Strong analytical and problem-solving skills with the ability to interpret complex medical data. - Excellent communication and interpersonal skills to build and maintain effective relationships with stakeholders. - Detail-oriented with a commitment to ensuring accuracy and compliance in all aspects of clinical trial enrollment. #LI-RD1 #LI-Remote What ICON can offer you: Our success depends on the quality of our people. That’s why we’ve made it a priority to build a diverse culture that rewards high performance and nurtures talent. In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family. Our benefits examples include: - Various annual leave entitlements - A range of health insurance offerings to suit you and your family’s needs. - Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead. - Global Employee Assistance Programme, TELUS Health, offering 24-hour access to a global network of over 80,000 independent specialised professionals who are there to support you and your family’s well-being. - Life assurance - Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidised travel passes, health assessments, among others. Visit our careers site to read more about the benefits ICON offers. At ICON, inclusion & belonging are fundamental to our culture and values. We’re dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know or submit a request here. Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless – there’s every chance you’re exactly what we’re looking for here at ICON whether it is for this or other roles. Are you a current ICON Employee? Please click here to apply

Clinical Trial Liaison- France ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development We are currently seeking a Clinical Trial Enrollment Liaison to join our diverse and dynamic team. As a Clinical Trial Enrollment Liaison at ICON, you will play a pivotal role in designing and analyzing clinical trials, interpreting complex medical data, and contributing to the advancement of innovative treatments and therapies. What you will be doing - Collaborate with cross-functional teams to design and implement effective clinical trial enrollment strategies. - Analyze and interpret clinical trial data, ensuring accuracy and compliance with regulatory standards. - Foster strong relationships with study sites and investigators to enhance patient recruitment and retention. - Act as a liaison between sponsors, investigators, and study participants, providing support and guidance throughout the enrollment process. - Contribute to the continuous improvement of enrollment processes and strategies to optimize trial outcomes. Your profile - Bachelor's degree in a relevant field, such as life sciences or healthcare. - Proven experience in clinical trial enrollment or related roles. - Strong analytical and problem-solving skills with the ability to interpret complex medical data. - Excellent communication and interpersonal skills to build and maintain effective relationships with stakeholders. - Detail-oriented with a commitment to ensuring accuracy and compliance in all aspects of clinical trial enrollment. #LI-RD1 #LI-Remote What ICON can offer you: Our success depends on the quality of our people. That’s why we’ve made it a priority to build a diverse culture that rewards high performance and nurtures talent. In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family. Our benefits examples include: - Various annual leave entitlements - A range of health insurance offerings to suit you and your family’s needs. - Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead. - Global Employee Assistance Programme, TELUS Health, offering 24-hour access to a global network of over 80,000 independent specialised professionals who are there to support you and your family’s well-being. - Life assurance - Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidised travel passes, health assessments, among others. Visit our careers site to read more about the benefits ICON offers. At ICON, inclusion & belonging are fundamental to our culture and values. We’re dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know or submit a request here. Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless – there’s every chance you’re exactly what we’re looking for here at ICON whether it is for this or other roles. Are you a current ICON Employee? Please click here to apply