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. Parexel FSP is hiring multiple Site Care Partners in Chile! Excellent opportunity for experienced Senior CRAs ready to take the next step in their career! The Site Care Partner (SCP) is the “face of the client” and therefore accountable for ensuring that sites receive necessary support and engagement, issues are resolved, and client’s reputation is upheld throughout study lifecycle. The SCP I is the main client point of contact for investigative sites; accountable for site start up activities through activation; accountable for building and retaining investigator site relationships and providing support from site recommendation through the lifecycle of studies; accountable for site level recruitment and operational success, and accountable for safeguarding the quality and patient safety at the investigator site. The SCP I contributes to country and site selection activities by proactively collaborating with key stakeholders and providing local intelligence to country outreach surveys, investigator strategies and client pipeline opportunities under supervision. Key Accountabilities (may include but not limited to the following): Intelligence Gathering: • Provides input into site recommendations via intimate understanding of country and region, sites, processes and practices, and associated site performance metrics • Provides support to the Study Operations Manager (SOM)/Global Study Manager (GSM) to define local requirements for the importation/exportation processes of the investigational medical product and ancillary supplies Study Start-Up and Activation: • Deploys Global Site and Study Operations (GSSO) site strategies by qualifying and activating assigned sites • Supports processes to optimize country and site selection activities including review and assessment of the draft potential site list and provide Pre-Trial Assessment (PTA) output for site selection • Maintains a thorough knowledge of assigned protocols • Conducts study start up activities at the site level including but not limited to PTA, coordination of site activation checklist items, Informed Consent Document (ICD) finalization, Site Initiation Visit (SIV), as applicable, including management of issues that may compromise time to site activation • Ensures all the site initiation activities completed including training per site activation checklist, collect and complete necessary documentation and systems needed • Supports country specific ICD review and deployment when applicable • Ensures follow up activities are completed post PTA and SIV to ensure site readiness for First Subject First Visit (FSFV) • Partners with site monitor to ensure site monitoring readiness in anticipation of FSFV • Responsible for relationship building and operational oversight of the site • Provides support for escalated site issues related to study delivery by coordinating communications and resolution efforts (e.g., vendor, site contracts and payment issues etc.) • Ensures the strategy and approach for Investigational Product (IP) and ancillary supplies for sites and country requirement throughout the lifecycle of the study • Accountable for effective site recruitment planning and delivery, consistent with global and/or country plan and local targets • Responsible for enrollment support and ensures progress by responding to recruitment issues from investigators • Maintains regular communications with investigator sites to gather status updates and drive delivery to study goals (e.g. recruitment, data entry timelines etc.) • Partners with local Regulatory Authority (RA)/ Clinical Trial Regulatory Operations (CTRO) / Site Activation Partner (SAP) to ensure timely completion on country / local registry when applicable Study Conduct and Closeout: • Acts as operational point of contact for all site level questions, liaising with and escalating to appropriate teams to respond and resolve questions • Reviews site monitoring reports • Supports the site with revision and submission of ICD documents (and amendments) • Works with other roles to maintain system management (e.g., Electronic Data Capture, Shared Investigator Platform, Site Profile and other systems as applicable) at site level ensuring alignment across platforms • During the conduct of the study, the Site Management Organization (SMO) Assessment is reviewed with the site, when applicable, on an annual basis following site initiation and updated as needed under client/ Senior SCP supervision. In addition, SMO Assessment is reviewed and updated when major staffing, contracting, or other significant site changes/issues occur to confirm that continuity and contingency plans are current • Reviews and manages site practices that differ from client practices and liaises with study management and Business Process Owners as needed • Maintains regular communications with investigator sites to gather status updates, informal and formal performance metrics, and study level feedback • Oversees and manages of site deliverables to study targets, (i.e. data cuts and sweeps, interim analyses, database locks), helping to oversee data is up to date and any other site facing deliverables, (i.e., investigator signatures) • Follows the study oversight plan and proactively puts in place mitigations for known and anticipated risks • Supports development and delivery, including issue resolution, of decentralized capabilities at investigator sites • Assures quality and consistency in the delivery of monitoring • Drives monitoring efficiencies and best practices for study, region and program • Supports shaping the local clinical development environment with a goal to enhance client reputation in scientific leadership • May act as a Subject Matter Expert (SME) on client systems and processes • Actively pursues efficiencies and develops best practices in the delivery of activities for site performance throughout the life cycle to increase investigator and site satisfaction strengthening site relationships Collaboration • Ensures clear and open communication with SOM • Supports the site monitor to develop positive Investigator relationships throughout the life of the study and escalate any training or compliance concerns with Country Trials Manager (CTM) and Study Management • Coordinates with other roles and functions that interface with study sites (e.g., Study Monitor, Investigator Contracts Lead, Site Activation Partner, Clinician, etc.) optimizing communications and enhancing overall visibility into and confidence of quality of site level activities Process, Standards, and Oversight: • Oversees site utilizing and interpreting data from analytic tools, with country intelligence to proactively identify risks to quality and compliance and to develop and implement mitigation plans for these risks Compliance with Parexel standards: • Complies with required training curriculum • Completes timesheets accurately as required • Submits expense reports as required • Updates CV as required • Maintains a working knowledge of and complies with Parexel processes, ICH-GCPs and other applicable requirements Skills: • Demonstrated experience in site management with prior experience as a site monitor • Demonstrated experience in start up activities through to site activation • Demonstrated experience in conduct and close out activities • Demonstrated knowledge of quality and regulatory requirements in applicable countries • Must demonstrate good computer skills and be able to embrace new technologies • Ability to communicate effectively and appropriately with internal and external stakeholders • Ability to adapt to changing technologies and processes • Effective verbal and written communication skills in relating to colleagues and associates both inside and outside of the organization • Effectively overcomes barriers encountered during the implementation of new processes and systems • Demonstrated networking and relationship building skills • Demonstrated ability to manage cross functional relationships • Identifies and builds effective relationships with investigator site staff and other stakeholders • Proficiency in local language preferred • English proficiency is required • Ability to manage required travel of up to 75% on a regular basis Knowledge and Experience (preferred): • Good communication, presentation and interpersonal skills • Knowledge of country requirements for GCP that may be different to those of client procedures Education: • Bachelor’s degree or Registered Nurse in a related field or equivalent combination of education, training and experience (estimate at least 5 years experience)

• We’re looking for a Client Success professional who wants to take their career to the next level. • You will be responsible for acting as the primary point of contact between Boostability and specific Agency and Supported Reseller partners. • You will own a dedicated book of business and will support the partner relationship through active troubleshooting, account management, and by demonstrating a strong working knowledge of digital marketing with a particular emphasis on SEO. • Successfully representing Boostability’s products and services as you support the success of digital marketing campaigns with an emphasis on SEO • Practicing proactive retention by ensuring every interaction is handled with the customer and partner experience top of mind • Troubleshooting account and partner level issues successfully, resolving and removing pain points for our customers and partners • Performing regular audits of digital marketing campaign performance and suggesting adjustments as needed to improve campaign performance • Conducting phone and video calls with clients via Zoom Contact Center and Zoom Meetings • Managing the fulfillment of our client’s SEO packages: Periodic appointments, on-site recommendations, and changes, allocation of off-site work, etc. • Providing periodic Client check-ins and reports • Ordering implementation of SEO tasks from our Fulfillment departments

• Manage complex calendars across multiple stakeholders, prioritizing competing demands with strong judgment • Coordinate domestic and international travel, including itineraries, logistics, and expense management • Plan and execute team meetings, offsites, and events (end-to-end logistics, agendas, and follow-ups) • Act as a liaison across cross-functional teams, ensuring clear communication and alignment • Support day-to-day operations of the team, including tracking priorities, action items, and deliverables • Prepare materials for meetings, including presentations, reports, and briefing documents • Handle sensitive and confidential information with discretion and professionalism • Identify opportunities to improve processes, increase efficiency, and reduce friction for the team • Assist with onboarding new team members and supporting team culture initiatives

Art Supervisor In the journey of your life, your career should make a difference. At Inizio Evoke, we come together—to do the best work, in the best possible place. We're all in. Because it's everyone's role to make health more human™. Who We Are Inizio Evoke is a global health marketing, communications, and transformation platform unlocking growth through data-driven insights and human centricity. We study the 'why' behind health decisions and create creative solutions that inspire meaningful change. About the Role We are looking for an Art Supervisor who is ready to take ownership of creative direction across brands, mentor junior talent, and ensure that all visual work meets the highest quality standards. If you are passionate about design, brand storytelling, and strategic thinking in the healthcare and pharmaceutical space, this is the perfect role for you. At Inizio Evoke, we foster a collaborative and innovative environment where designers, writers, and strategists work together to create high-impact creative solutions. You will report to the SVP, Group Creative Director in this role. What You'll Do - Take the lead on visual creative development, ensuring all work is strategic, innovative, and effective. - Be the design expert and brand steward, maintaining consistency across all creative materials. - Oversee a team of Art Directors and Senior Art Directors, providing mentorship, guidance, and feedback. - Work closely with Copy, Strategy, and Medical teams, ensuring alignment between messaging and visuals. - Manage and refine design execution across multiple channels, including digital, print, video, and social media. - Present and defend creative work to our teams, clients, and regulatory reviewers. - Contribute to brand strategy and campaign development, bringing fresh creative solutions to complex challenges. - Stay ahead of industry trends and emerging technologies, elevating the creative output of the team. Who You Are - An experienced and visionary art director, with expertise in brand storytelling and design strategy. - A natural mentor and leader, who fosters creative growth in junior designers. - A master of digital and print production, proficient in Adobe Creative Suite, Figma, and AI-driven design tools. - A strategic thinker, who balances creative ambition with regulatory requirements in pharma marketing. - An adaptable problem solver, comfortable working in a dynamic and regulated environment. - A strong presenter and collaborator, a natural advocate for creative work. - A good human, bringing professionalism, integrity, and enthusiasm to every project. Work Environment & Benefits Inizio Evoke offers a fully remote work environment and outstanding company-paid benefits, including medical, dental, 401(k), tuition reimbursement, and flexible time off. 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. The base salary range represents the low and high end of the salary range for this position. This range may differ based on your experience and skill set, geographic location, and cost of living considerations. We consider compensation more than just a base salary – that’s why we also offer an exceptional range of flexible benefits, personal support and tailored learning and development opportunities all designed to help you realize your full potential both in life and at work. Compensation $95,000—$130,000 USD Don't meet every job requirement? That's okay! Our company is dedicated to building a diverse, inclusive, and authentic workplace. If you're excited about this role, but your experience doesn't perfectly fit every qualification, we encourage you to apply anyway. You may be just the right person for this role or others.