IQVIA

Are you a freelance translator with a passion for life sciences content? Join us on an exciting journey and become a member of our growing global community of linguists. The IQVIA Translation Services team is looking for freelance translators from English into Hebrew. You will work with a truly global industry leader to deliver content in our target languages and markets in the most effective and timely fashion. For qualified and interested candidates permanent positions may be considered as well. In order to be considered you need to meet the below criteria: Native fluency in target language – spoken and written Fluency in source language(s) – spoken and written At least 1 year of experience translating, reviewing and editing life sciences content including clinical trial documents. Must be clearly outlined in your CV with document types. A university degree in translation or linguistics and at least 2 years of translation experience OR no university degree and at least 5 years of translation experience Be able to work according to tight deadlines and independently is a must Experience with translation management systems and CAT tools is a must Prior experience as a translator with a translation and localisation company is desirable, yet not essential If you are interested in joining us, please submit your application in English and include your rates in your application. We will not accept applications from Agencies. If you represent an agency or team of linguists, PLEASE DO NOT APPLY. This posting is for individual freelancers only. IQVIA is a leading global provider of advanced analytics, technology solutions and clinical research services to the life sciences industry. We believe in pushing the boundaries of human science and data science to make the biggest impact possible – to help our customers create a healthier world. Learn more at https://jobs.iqvia.com IQVIA is a leading global provider of advanced analytics, technology solutions and clinical research services to the life sciences industry. We believe in pushing the boundaries of human science and data science to make the biggest impact possible – to help our customers create a healthier world. Learn more at https://jobs.iqvia.com

Job Overview Provides administrative and/or technical support. Essential Functions • Responsible to reconcile SAP Grant Payment Report to Excel Grant Payment Report for assigned Sponsors’ studies, as well as reconcile the total GPS Sponsor balance to the Corporate Sponsor Balance on a monthly basis per SSAE16 Controls • Responsible to accurately complete all necessary journal entries as assign • Responsible to quality review CTA and Payment Intake form setups to determine appropriate SAP vendor and payment method for Payments staff for assigned Sponsor’s studies, inclusive of bank entry validation for the Accounting dept. • Responsible for SharePoint tracker completion for assigned sponsors. • On an annual basis, assist with 1099 and other country tax reporting as assigned • Special projects involving maintenance of the vendor database in SAP, and SOP Maintenance, as required • Other duties as assigned Qualifications • Bachelor's Degree Pursuing degree Req • Appropriate verbal and written communication skills to function within a professional work environment. • Evidence of effective problem – solving, analytical, and critical thinking skills. • Proficiency in alignment with the desired role placement • Evidence of strong team work and communication skills. At IQVIA, we believe in pushing the boundaries of human science and data science to make the biggest impact possible – to help our customers create a healthier world. Learn more at https://jobs.iqvia.com

Sales Representative Role purpose Partners with healthcare customers to understand their needs and help more patients benefit from the right treatment, through insight-led, compliant and well-planned engagement, live or virtual, according to what the customer prefers. Key responsibilities • Develop and strengthen professional relationships with General Practitioners (and pharmacists where applicable), working closely with the Area Manager / Team Lead and the local team to achieve project objectives. • Present the product and provide ongoing scientific information and education, in compliance with applicable regulations and company procedures. • Maintain a high level of scientific and regulatory knowledge. • Monitor market developments and regularly share structured market insights and feedback. Experience and requirements • Proven experience in a similar role and knowledge of the GP target audience in the assigned territory. • University degree in a scientific discipline per local legislation. • Solid scientific background. • Languages: Hebrew and English required; Arabic required depending on the region. • Proficiency with digital tools, CRM systems and the Microsoft Office suite. • Excellent communication and negotiation skills; active listening. • Strong results orientation, good organizational skills, analytical thinking and problem-solving. 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 IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

Job Overview Provides the key client relationship to a major client or clients. Grows revenue by leveraging the full IQVIA portfolio and identifying new business opportunities. Co-ordinates the sales, business & service lines at a regional level to ensure effective execution against client needs and IQVIA revenue targets. Essential Functions • Ensures the quarterly and full year revenue targets are met to achieve or exceed the assigned revenue and growth goals in assigned accounts or sales territory. • Takes proactive role in contract strategy. • Assists management in developing strategies for expanding scope of existing contracts and identifying new business and win-back opportunities. • As required, may lead negotiations in renewing contract(s) within assigned accounts. • Develops relationships with key executives and decision makers within assigned accounts. • Assists in managing the overall relationship to ensure a high level of customer satisfaction with product/service offerings. • Coordinates the involvement of IQVIA resources (marketing, sales specialists, consulting and client service) in actively promoting the full IQVIA portfolio of offerings to anticipate and meet client needs. • Maximizes sales by effectively utilizing sales and marketing materials, appropriate databases and technologies. • Executes account plan(s) and monitors progress. • Adjusts plan accordingly to consider new IQVIA product/service offerings as well as significant changes to business conditions. Area Manager / Team Lead Role purpose Leads a team of sales representatives to deliver results for customers and patients: sets clear expectations, builds capability through coaching, allocates resources where they have the most impact, and ensures the team works to the highest compliance standards. Key responsibilities • Directly manage a team of Sales Representatives responsible for physician education and product promotion. • Business development and revenue management within the assigned territory. • Build and maintain relationships with key opinion leaders (KOLs). • Report to the IQVIA project leader. Experience and requirements • Proven experience in a leadership or management role. • Proven track record of achieving individual performance objectives. • Strong negotiation and communication skills. • Demonstrated leadership and teamwork capabilities. • Self-motivated, organised, proactive and able to work independently. • University degree in a scientific discipline per local legislation. • Languages: Hebrew and English required; Arabic required depending on the region 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 IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

Job Overview Perform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol, applicable regulations and guidelines, and sponsor requirements. Essential Functions • Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with contracted scope of work and regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines • Work with sites to adapt, drive, and track subject recruitment plan in line with project needs to enhance predictability. • Administer protocol and related study training to assigned sites and establish regular lines of communication with sites to manage ongoing project expectations and issues. • Evaluate the quality and integrity of study site practices related to the proper conduct of the protocol and adherence to applicable regulations. Escalate quality issues as appropriate. • Manage the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and enrollment, case report form (CRF) completion and submission, and data query generation and resolution. May support start-up phase. • Ensure copies/originals (as required) site documents are available for filing in the Trial Master File (TMF) and verify that the Investigator's Site File (ISF) is maintained in accordance with GCP and local regulatory requirements. • Create and maintain appropriate documentation regarding site management, monitoring visit findings and action plans by submitting regular visit reports, generating follow-up letters and other required study documentation. • Collaborate and liaise with study team members for project execution support as appropriate. • If applicable, may be accountable for supporting development of project subject recruitment plan on a per site basis. • If applicable, may be accountable for site financial management according to executed clinical trial agreement and retrieve invoices according to local requirement. Qualifications • High School Diploma or equivalent Degree in scientific discipline or health care preferred. • Requires at least 2 year of on-site monitoring experience. • Equivalent combination of education, training and experience may be accepted in lieu of degree. • Good knowledge of, and skill in applying, applicable clinical research regulatory requirements (i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines). • Good therapeutic and protocol knowledge as provided in company training. • Computer skills including proficiency in use of Microsoft Word, Excel and PowerPoint and use of a laptop computer and iPhone and iPad (where applicable). • Written and verbal communication skills including good command of English language. • Organizational and problem-solving skills. • Effective time and financial management skills. • Ability to establish and maintain effective working relationships with coworkers, managers, and clients. 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 IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

Why Join Clinical Functional Service Partnerships (CFSP)? At IQVIA, our Clinical Functional Service Partnership (CFSP) models offer the best of both worlds: the opportunity to work as an integrated member of a leading sponsor's team while benefiting from the global expertise, career development and support of IQVIA. CFSP roles provide the opportunity to develop specialist expertise on a dedicated program, with the flexibility to expand across sponsors and therapeutic areas as your career progresses. Through our long-standing partnerships with top pharmaceutical and biotechnology companies, you will contribute to the delivery of cutting-edge clinical research programs that bring innovative treatments to patients worldwide. Our professionals support studies across all phases of development and a broad range of therapeutic areas, gaining valuable experience in diverse and dynamic research environments. Regulatory and Start-Up Specialist At IQVIA, our Study Start Up Specialists play a critical role in bringing clinical trials to life. Working within a sponsor-dedicated environment, you will manage site identification, regulatory submissions (if applicable for country/region), ethics approvals and site activation activities that help studies start faster and accelerate patient access to innovative treatments. Acting as a key liaison between investigative sites, sponsors, and internal stakeholders, you will ensure regulatory and contractual milestones are delivered efficiently while maintaining compliance with local and international requirements. Backed by IQVIA's global infrastructure, you will gain valuable sponsor-facing exposure, cross-functional collaboration experience, and opportunities for long-term career growth within clinical research. Key Responsibilities • Serve as the primary point of contact for investigative sites, Site Activation Managers, Project Managers and internal stakeholders. • Execute site identification, feasibility assessment, and site activation activities for assigned clinical studies. • Prepare, review, and distribute regulatory documentation to ensure completeness, accuracy, and compliance. • Track and manage submission, approval, and execution of essential documents, including:• Regulatory submissions (if applicable for country/region) • Ethics Committee submissions • Informed Consent Forms (ICFs) • Investigator Pack (IP) release documentation • Clinical Trial Agreements (CTAs) • Review, negotiate, and manage site regulatory documents, contracts, and associated start-up deliverables. • Maintain accurate records within internal systems and tracking tools. • Monitor project milestones and proactively identify risks and mitigation plans. • Provide local regulatory expertise to project teams and Site Activation Managers. • Perform quality reviews of site documentation. • Review site performance metrics and contribute to continuous process improvement initiatives. • Collaborate closely with sponsors and cross-functional teams to ensure successful study start-up and site activation delivery. What We’re Looking For • Bachelor's Degree in Life Sciences or a related scientific discipline. • Experience in clinical trial regulatory affairs, site start-up, site activation, or related clinical research functions. • Strong understanding of local and international regulatory requirements, GCP, and clinical research processes. • Experience managing regulatory documentation, contracts, and start-up deliverables. • Excellent communication, negotiation, and problem-solving capabilities. • Fluency in Hebrew with strong English communication skills. Build Your Future with IQVIA If you want to make a genuine difference in how quickly lifechanging trials get off the ground, we would love to hear from you. As an RSU Specialist within Clinical FSP, you will be part of IQVIA's mission to push the boundaries of human science and data science, helping create a healthier world, one activated site at a time. At IQVIA, you will have the opportunity to work on innovative studies, collaborate with industry-leading sponsors, leverage cutting-edge technology and develop your career within a global organization dedicated to transforming healthcare and improving patient outcomes worldwide. 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 IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

IQVIA™ is The Human Data Science Company™, focused on using data and science to help healthcare clients find better solutions for their patients. IQVIA offers a broad range of solutions that harness advances in healthcare information, technology, analytics, and human ingenuity to drive healthcare forward. The Patient Centered Solutions team (PCS) The PCS team leads the industry in the science of measuring the patient experience. We pair strategic consulting expertise with technical scientific knowledge to design and execute scientifically rigorous research that incorporates the patient voice into the development and commercialization of new medicines. This research includes qualitative (e.g., patient interviews, focus groups), quantitative (e.g., clinical outcome assessments (COAs)/patient-reported outcomes (PROs), preference research) and passive (e.g., digital health technology tools) approaches to understand patient, caregiver and physician experiences and expectations of disease and treatment. Why join? • Become part of a recognized global leader in patient-focused research • Keep growing with an organization that encourages and invests in continuous professional and personal development • Apply your business and leadership skills in an entrepreneurial and multi-disciplinary team • Continue challenging yourself by addressing the toughest client issues, working across multiple geographies and solutions in a dynamic and crucial field for the industry • Make a difference to patients by enabling the successful approval or launch of new treatments with features that are truly patient-centric Responsibilities The Associate Principal/ Principal Clinical Outcome Assessment (COA) Endpoint Strategy serves as the subject matter expert for COA endpoint strategy, endpoint development, COA regulatory strategy, and COA instrument science in client engagement and project delivery. This role brings deep expertise in COA measurement science to differentiate client solutions through expert-driven, highly insightful endpoint strategies. The role acts as a trusted advisor to pharmaceutical and biotechnology sponsors and represents IQVIA as an external scientific thought leader while ensuring internal scientific quality and best practices. Key responsibilities include: Client Strategy Leadership & Scientific Differentiation • Develop COA endpoint strategies across clinical development programs, including primary and key secondary endpoint positioning in consulting projects. • Bring COA expertise into client meetings, workshops, and strategic discussions. • Differentiate proposals and client solutions through expert-driven COA strategy narratives. • Translate emerging scientific and regulatory expectations into actionable client recommendations. Regulatory-Grade Endpoint Strategy & FDA Engagement • Advise sponsors on development and justification of COA endpoint strategies for regulatory interactions. • Support preparation for and participation in FDA meetings as the COA subject matter expert. • Guide sponsors on evidence expectations, context of use, and fit-for-purpose COA strategies. COA Instrument Development Leadership • Provide scientific leadership in the development of new COA instruments from concept to validation-ready tools. • Lead and advise on drafting and refinement of COA instrument items, response options, recall periods, and scoring approaches. • Oversee qualitative research activities supporting content validity, including concept elicitation and cognitive interviewing. • Ensure new COA instruments are patient-centered, scientifically robust, and fit-for-purpose for clinical and regulatory use. Internal SME Oversight & Quality Assurance • Serve as subject matter expert overseeing internal project teams executing COA strategy and development work. • Review and approve key scientific deliverables to ensure quality, rigor, and alignment with best practices. • Mentor and coach COA consultants, supporting capability development across the organization. Business Development & Practice Growth • Support business development through proposal leadership, solution design, and client presentations. • Contribute to the evolution of COA strategy methodologies, frameworks, and reusable assets. External Scientific Leadership & Visibility • Maintain a strong external profile through publications, conference presentations, and scientific collaborations. • Represent IQVIA as a recognized expert in COA science and endpoint strategy. • Contribute to academic teaching, advisory boards, or industry working groups where appropriate. Essential experience, skills and education required • Deep expertise across COA types (PRO, ObsRO, ClinRO, PerfO) and their application in clinical research. • Extensive experience developing COA endpoint strategies across multiple therapeutic areas. • Hands-on experience developing new COA instruments, including item writing and qualitative validation. • Experience supporting FDA-facing endpoint strategy and regulatory interactions. • Ability to mentor junior team members. • Excellent scientific writing, presentation, and stakeholder engagement skills. • Advanced degree (PhD, MD, PharmD, DrPH, MSc) in a relevant scientific discipline strongly preferred. • Strong publication record and recognized credibility in outcomes research or COA measurement science. • Well-developed written and verbal communication skills including presentations, chairing meetings, external conference presentations, workshop facilitation, business and report writing. • An entrepreneurial nature and interest in developing new client offerings and solutions and in building the capability to deliver the same. 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 IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.