Clinical Trial Associate 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 As a Clinical Trial Associate at ICON, you will assist with the design and analysis of clinical trials, interpreting complex medical data, and contribute to the advancement of innovative treatments and therapies. What You Will Do: Your role will involve delivering clinical research work to a high standard, working closely with your team and stakeholders. Key responsibilities include: - Assist in the coordination and administration of clinical trials, ensuring compliance with protocols and regulatory requirements. - Maintain and organize clinical trial documentation, including study files, essential documents, and regulatory submissions. - Support the preparation of study-related materials, such as informed consent forms and case report forms. - Work with cross-functional teams to facilitate communication and ensure smooth trial execution. - Contribute to the tracking and reporting of clinical trial metrics and milestones. Your Profile: You will bring relevant clinical research experience, along with the following qualifications and skills. Required qualifications and experience: - Bachelor's degree in a scientific or healthcare-related field. - Prior experience or strong interest in clinical research. - Knowledge of clinical trial processes, regulations, and guidelines. - Excellent organizational and communication skills. - Ability to work collaboratively in a fast-paced environment with attention to detail. - Willingness to travel as required (approximately 10%) 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

Title: Clinical: Clinical Quality Support Specialist - Remote (Spanish Speaking) Location: , NJ usa Job Description: ID:9907 Office:Remote Hours Required:N/A Registered Nurse (RN) – Remote (Part-Time) Care Finders Total Care LLC, a Modivcare Home Care Company – New Jersey Care Finders Total Care, a Modivcare Home Care company, is seeking a Registered Nurse (RN) to manage a caseload of members and conduct 30-day patient satisfaction and quality assurance (QA) surveys via telephone. This role focuses on assessing members’ physical and psychosocial needs while maintaining accurate nursing documentation in our internal systems. Responsibilities: - Conduct inbound and outbound calls to complete 30-day patient satisfaction surveys - Assess members’ physical and psychosocial status - Follow up on certified health conditions, current care plans, and program services - Document all interactions and findings in the internal database Compensation & Schedule: - Pay: $39–$41 per hour (based on experience) - Schedule: Part-time, remote position (hours may vary based on business needs) Requirements: - Active RN license in New Jersey - Minimum of 1 year of RN experience in the United States - Current CPR certification - Home care experience preferred Bilingual (Spanish) Required Benefits and Perks… - 401(k) with a 6% match - Employee Assistance Program - Employee Discounts (retail, hotel, food, restaurants, car rental, and much more!) - Voluntary Term Life and AD&D Insurance - Legal Services Insurance - Short-Term and Long-Term Disability - Accident, Critical Illness & Hospital Indemnity Insurance We live and lead by our Values… - We treat everyone with dignity and RESPECT - We earn the TRUST of our members, and each other - We provide RELIABLE services that open doors - We serve with courtesy and COMPASSION - We prioritize SAFETY - We communicate with purpose and TRANSPARENCY We are committed to equal employment opportunity regardless of race, color, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, disability, gender, gender identity or expression, or veteran status. We are proud to be an equal opportunity workplace

Work Schedule Standard (Mon-Fri) Environmental Conditions Office Job Description Location: Czech Republic or Slovakia Thermo Fisher Scientific Language Services is looking for a Czech–Slovak Language Specialist with experience in clinical translation and quality assurance to join our internal team. This role is primarily focused on clinical content, while also supporting medical device and life sciences projects. The position requires a flexible mindset and interest in expanding into medical-technical content areas. Essential Functions - Coordinating and managing the final quality of assigned translations to ensure high quality and compliance with client and regulatory standards. - Performing quality checks on clinical documentation (e.g., ICFs, protocols, IBs, patient diaries, CTAs). - Supporting review and validation of medical device content such as Instructions for Use (IFUs), labeling, and technical documentation as needed. - Running and maintaining language assets, including translation memories, terminology, and style guides. - Developing and maintaining terminology for Czech and Slovak. - Ensuring translation memories are kept up to date. - Setting and executing linguistic quality assurance processes for the assigned languages. - Using CAT/TMS tools to monitor the quality of outsourced translations and external suppliers. - Aligning external linguists on client-specific instructions, terminology, and formatting requirements. - Analyzing linguistic quality issues and contributing to continuous improvement initiatives with Project Management. - Performing occasional linguistic tasks, including translation, revision, and implementation of client feedback. Education and Experience Requirements Applicants should meet one of the following: - Bachelor’s degree in Translation, Linguistics, Language Studies, or related field from a recognized higher education institution; OR - Bachelor’s degree in another field with minimum 2 years of translation experience (preferably in clinical research, medical devices, or life sciences); OR - Minimum 5 years of professional translation experience (preferably in clinical and/or medical-technical domains). Knowledge, Skills and Abilities - Native Czech or Slovak, with strong proficiency in the other language. - Proven experience in clinical translation; exposure to medical device or life sciences content is an advantage. - Familiarity with clinical trial documentation and interest in medical device content (e.g., IFUs). - CAT/TMS tool experience required. - Proven terminology and translation memory management experience. - Strong attention to detail, organization, and ability to manage multiple priorities. - Excellent written, oral, and interpersonal communication skills. - Scientifically curious with interest in medical and technical subject matter. - Proficiency in MS Office suite.

When our values align, there's no limit to what we can achieve. At Parexel, we all share the same goal - to improve the world's health. From clinical trials to regulatory, consulting, and market access, every clinical development solution we provide is underpinned by something special - a deep conviction in what we do. Each of us, no matter what we do at Parexel, contributes to the development of a therapy that ultimately will benefit a patient. We take our work personally, we do it with empathy and we're committed to making a difference. Key Accountabilities: Maintenance (from initiation through close out): Act as PAREXEL’s direct contact with assigned sites, assess and ensure overall integrity of study implementation and adherence to study protocol at clinical sites, and perform problem-solving to address and resolve site issues. - Build relationships with investigators and site staff. - Facilitate and support site with access to relevant study systems and ensure sites are compliant with project specific training requirements. - Evaluate if on-site staff assignment is still accurate and determine and implement corrective actions & follow-up, if necessary / relevant. - Address and resolve issues at sites, including the need for additional training, potential deficiencies in documentation, and communication. - Address/evaluate/resolve issues pending from the previous visit, if any. - Follow-up on and respond to appropriate site related questions. - Apply working knowledge and judgment to identify and evaluate potential data quality and data integrity issues. Determine and implement appropriate follow-up action. - Actively participate in Investigator and other external or internal meetings and audits & regulatory inspections as required. - Collect, review, and approve (if applicable) updated/amended site documentation, including regulatory documents as applicable. - Evaluate site recruitment plan in collaboration with the site staff on an ongoing basis and provide strategy for improvements. - Perform on-site visits; this includes Qualification and Initiation visits; apply judgment and knowledge to independently resolve site issues, questions and concerns. - Conduct remote visits/contacts as requested/needed. - Generate visit/contact report. - Evaluate overall compliance and performance of sites and site staff: provide recommendations regarding site-specific actions and use judgment and experience to assess the ability and motivation of site staff. - Assess & manage test article/study supply including supply, accountability and destruction/return status. - Review & follow-up site payment status. - Follow-up on CRF data entry, query status, and SAEs. - Conduct on-site study-specific training (if applicable). - Perform site facilities assessments - Recognize impact of study non-compliance/issues/delays/changes on study timelines and communicate study issues that require immediate action, with proposed strategy for resolution Overall Accountabilities from Site Identification to Close out: Ensure timely and accurate completion of project goals and update of applicable trial management systems. - Work with team members to meet project goals, provide strategy for efficient project planning and goal completion, and encourage the support of team members where required. - Update all appropriate Clinical Trial Management Systems (CTMS) on an ongoing basis, including performing regular reviews of site level data in clinical systems (e.g. CTMS, EDC, IVRS, and SIS) and ensure timely and high quality data entry compliance from sites, manage and submit all relevant documents to the Trial Master File (TMF), ensuring first time quality, and distribute study documents to site including configuration of Investigator Site Files if applicable and on-going maintenance for completeness and quality. - Ensure that assigned sites are audit and inspection ready - Monitor and maintain compliance with ICH-GCP and applicable international and local regulations. - Delegate administrative and other tasks to Administrative Support Team as needed and where appropriate. Guide Administrative Support Team members, review work, and provide feedback to manager regarding performance. - Show commitment and perform consistent high-quality work. - Maintain a positive, results-orientated work environment, building partnerships and collaborative relationships, communicating with team(s) in an open, balanced, objective manner, modeling the high performance culture values. - Maintain a working knowledge of and ensure compliance with applicable ICH-GCP Guidelines, international and local regulations, Parexel SOPs, other Parexel / Sponsor training requirements and study specific procedures, plans and training. - Ensure basic understanding of project scope, milestones, budgets, and strive for high quality, timely, and efficient delivery. - Provide input and feedback for Performance Development Conversation(s). - Proactively keep manager informed about work progress and any issues. - Develop expertise to become a subject matter expert. - Work in a self-driven capacity, with limited need for oversight. - Complete additional tasks in a timely manner (e.g. timesheets, expenses, metrics, etc.) Skills: - Sound problem solving skills. - Able to take initiative and work independently, and to proactively seek guidance when necessary. - Advance presentation skills. - Client focused approach to work. - Ability to interact professionally within a client organization. - Flexible attitude with respect to work assignments and new learning. - Ability to prioritize multiple tasks and achieve project timelines; utilizing strong analytical skills to make decision autonomously due to the unpredictable nature of the issues that arise. - Willingness to work in a matrix environment and to value the importance of teamwork. - Strong computer skills including but not limited to the knowledge of a Clinical Trial Management System (CTMS), Electronic Document Management System (EDMS), and MS-Office products such as Excel and Word. - Strong interpersonal, verbal, and written communication skills. - Sense of urgency in completing assigned tasks and ability to assist others to meet study/country deliverables and preserving patient safety. - Effective time management in order to meet study needs, team objectives, and department goals. - Developing ability to work across cultures. - Shows commitment to and performs consistently high-quality work. - Ability to successfully work in a (‘virtual’) team environment. - Consulting Skills - Great attention to detail. - Able to accommodate extensive travel time requirements, according to tasks allocation/phase of the study assigned. - Holds a driver’s license where required. Knowledge and Experience: - Site Management experience or equivalent experience in clinical research, with understanding of clinical trials methodology and terminology Education: - Educated to degree level (biological science, pharmacy, or other health-related discipline preferred) or equivalent nursing qualification or other equivalent experience