ProPharma

• Conduct Audits of Pharmaceutical, medical device, clinical, and software development organizations for compliance with health authority regulations applicable to computer systems, artificial intelligence, data integrity • Conduct gap assessments and provide remediation guidance for compliance with health authority regulations applicable to computer system, artificial intelligence, and data integrity • Authoring policies, procedures, and work instructions compliance with health authority regulations applicable to computer system, artificial intelligence, and data integrity • Provide clients with advice and guidance on computer system validation, AI compliance, and data integrity compliance approaches. Manage teams of internal resources in executing these strategies. • Assist in developing and maintaining internal procedures and tools for delivery of CSV, AI assurance, and data integrity services. • Develop and deliver original CSV content on current topics impacting the area of Computer System Validation, AI compliance, and electronic data integrity. Examples include blogs, training materials, webinars. • Teach computer system validation, software/AI quality compliance, and data integrity classes, as needed. • Participate in development of business strategies for growth of ProPharma’s CSV, AI Assurance, and Data Integrity practice. • Assist in development of the Marketing and Sales materials. Assist in Business Development activities. Assist Operations in staffing client projects. Lead interviews of ProPharma Group candidates. Some travel required. Other duties as assigned.

Role Description We’re looking for a Site Team Lead to support our Decentralized Clinical Trial operations on a new client partnership. You will drive excellence in site activities across Europe through the management of study coordinators, client communication and general project management. This is a fully remote position offered on a full time, permanent basis, and travel is not required. This role can be based in the UK, Netherlands, Germany, Sweden, Ireland and a number of locations across Central Eastern Europe. - Guide and support research staff on GCP/ICH compliance and study protocols. - Partner with coordinators and assistants to plan and execute activities. - Anticipate issues and implement corrective actions. - Oversee study tools, metrics, and deliverables. - Manage meeting minutes, communications, and Sponsor/CRO interactions. Qualifications - Extensive Study Coordinator experience. - Strong knowledge of ICH/GCP and clinical research regulations. - Skilled in applying SOPs and global guidelines. - Highly organized, able to multitask, and thrive independently or in a team. - Clear, professional communicator with a proactive mindset. Benefits - Be part of a forward-thinking team advancing patient-centered research through Decentralized Clinical Trials. - Have a direct impact on trial success and patient outcomes.

Title: Product Integrity Specialist Location: United States Canada time type Full time job requisition id JR 9800 For the past 25 years, ProPharma has improved the health and wellness of patients by providing advice and expertise that empowers biotech, med device, and pharmaceutical organizations of all sizes to confidently advance scientific breakthroughs and introduce new therapies. ProPharma partners with its clients through an advise-build-operate model across the complete product lifecycle. With deep domain expertise in regulatory sciences, clinical research solutions, quality & compliance, pharmacovigilance, medical information, and R&D technology, ProPharma offers an end-to-end suite of fully customizable consulting solutions that de-risk and accelerate our partners’ most high-profile drug and device programs. This Product Integrity Specialist position is critical in evaluating data for Product Complaints and Adverse Events. The Product Integrity Specialist may create cases, coordinate product retrievals, perform follow-ups via phone, generate follow-up related correspondence and complete additional services for select clients. The Product Integrity Specialist may also prepare, and review, reconciliation reports as needed by clients. This position requires someone with an extreme technical ability for proofreading and keeping a variety of processes and timelines straight within a regulated environment. Essential Functions: - Perform case review for Product Complaint (PC) and Adverse Event (AE) cases created by Medical Information to determine next action(s) required (if applicable): - Coordinate Retrieval for select client companies, if applicable - Place outbound follow up calls to complete Product. - Complaint reports and collecting additional information as requested by the client. - Create letters in response to Product Complaints as directed by the client. - Additional contracted PC and AE services for select client companies. - Case entry of electronic correspondence - Create and run reconciliation reports as needed. - The Product Integrity Specialist can confidently identify any new or follow-up Adverse Event details and report to appropriate contacts. - The Product Integrity Specialist can confidently identify any new or follow-up Product Complaint details and report to appropriate contacts. - Provide administrative support for MI group as needed. - Manage Product Integrity inbox(es) - Update existing Product Complaint and Adverse Event cases as appropriate. - Answer inbound calls and check voicemails. - Other duties as assigned. Necessary Skills and Abilities: - Excellent English language skills especially verbal and written (including proofreading) communication skills. - Ability to write fluent and grammatically correct American English. - Working knowledge of medical terminology, regulations, and industry standards. - Excellent interpersonal skills including empathetic customer service skills. - Accurate and proficient data entry skills. - Ability to multi-task with attention to detail within restrictive timeframes. - Proactive with demonstrative ability to independently identify problems and suggest effective solutions. - Ability to organize and prioritize in quickly changing environment within resource constraints. - Ability to take instruction and learn. - Receptive to constructive feedback. - Self-motivating. Ability to demonstrate initiative and internal drive. Willingness to seek out additional workload projects. - Effectively work independently and as part of a team. - Highly proficient in computer applications, including Microsoft Office software platforms and Adobe Acrobat, and experience using a document management system. Aptitude to learn other computer systems including inquiry handling database. Educational Requirements: - Pharmacy Technician, Veterinary Technician, Life Science Grad, or other Healthcare related equivalent required. Experience Requirements: - Minimum 1-3 years’ previous experience in an administrative or data entry role. - At least 1-3 years’ experience in medical or pharmaceutical industry field especially in Medical/Drug Information, Pharmacovigilance, Product Complaints, and/or Quality Assurance preferred. #LI-KP1 #LI-REMOTE We celebrate our differences and strive to create a workplace where each person can be their authentic self. We are committed to diversity, equity, and inclusion. Employees are encouraged to unleash their innovative, collaborative, and entrepreneurial spirits. With a holistic approach as an Equal Opportunity Employer, we provide a safe space where all employees feel empowered to succeed. All applications to roles at ProPharma are personally reviewed by a member of our recruitment team. We do not rely on AI screening tools to support our hiring process. You will always receive an outcome to your application so that you have an answer from us - whether you're successful or not. Whilst ProPharma supports remote working, we also recognise the value that comes from in person collaboration. As such, we encourage any new hires that are based within a reasonably short commute of one of our offices to work on a hybrid basis and spend some time working from that office location, as agreed with your manager. All applications will be treated on their own merit and candidates will not be at any advantage or disadvantage based on their proximity to an office. ***ProPharma Group does not accept unsolicited resumes from recruiters/third parties. Please, no phone calls or emails to anyone regarding this posting.

Title: Project Finance Manager Location: United States Remote Full time Job Description: For the past 25 years, ProPharma has improved the health and wellness of patients by providing advice and expertise that empowers biotech, med device, and pharmaceutical organizations of all sizes to confidently advance scientific breakthroughs and introduce new therapies. ProPharma partners with its clients through an advise-build-operate model across the complete product lifecycle. With deep domain expertise in regulatory sciences, clinical research solutions, quality & compliance, pharmacovigilance, medical information, and R&D technology, ProPharma offers an end-to-end suite of fully customizable consulting solutions that de-risk and accelerate our partners’ most high-profile drug and device programs. The Project Finance Manager position will provide global project finance support to the Executive Director, Global Project Finance across multiple Service Lines at ProPharma. This position will support revenue recognition, revenue and backlog forecasting, revenue overburn, and project profitability as well as business partnerships with Project Management, Functional Leadership, Corporate Operations, Billing, and FP&A teams. This position will also include regional finance support to manage certain Clinical Trials or Studies that require customer facing financial support, analysis, and reconciliations. Essential Functions: - Support the Project Finance function for Clinical Trials under the CRS Service Line, serving as PFM lead/liaison to both internal/external stakeholders to oversee certain regional Customers/Projects/Programs. This will include budget oversight, revenue recognition, billing, backlog forecasting, and insight into project profitability. - Support Project Management and Functional Leadership regarding budget control, budget supervision, or finance related Customer/Client requests. - Support the Project Finance function as business partner to other service lines, such as Pharmacovigilance, Quality & Compliance, Regulatory Sciences, Medical Information, and Research Development & Technology. This will include budget management, support for revenue and backlog forecasting processes, and NNB. - Assist in the build out of a Company Backlog Roll forward. - Assist in analysis around project profitability, pricing/margin analysis, and revenue overburn. - Supports the Financial month end close process to help accelerate timelines. - Harmonize and improve the Global Project Finance processes and drive future improvements within our ERP system, Workday. - Collaborate with FP&A and Billing teams to analyze project and client profitability and drive actionable insights within Service Lines. - Collaborate with BD/Sales to support the capture/reconciliation of NNB across Service Lines and understand how that translates to future revenues. - Other duties as assigned. Necessary Skills and Abilities: - Above average experience and abilities in Microsoft Excel, Word, PowerPoint, Power BI programs - Effective written and oral communication skills; ability to write, type, express or exchange ideas of a technical nature by means of the spoken word; convey information/instructions accurately; receive detailed information through oral or written forms and to translate those instructions into physical execution of tasks. - Demonstrated leadership capabilities including the ability to influence others outside of direct management sphere of influence. - Collaborative as a partner to facilitate organizational growth. - Creative in your approach to problem solving. - Able to manage multiple projects simultaneously, work autonomously and produce solid results within reasonable timeframes. - Ability to walk, stand and move about for long periods of time with equipment in the field, read, prepare and analyze data for development of reports; ability to sit and type for long periods of time. Educational Requirements: - B.S./B.A.in accounting or finance preferred. Experience Requirements: - 8 or more years’ experience in managing an accounting and/or finance function in a growing, medium or large size company. We celebrate our differences and strive to create a workplace where each person can be their authentic self. We are committed to diversity, equity, and inclusion. Employees are encouraged to unleash their innovative, collaborative, and entrepreneurial spirits. With a holistic approach as an Equal Opportunity Employer, we provide a safe space where all employees feel empowered to succeed. All applications to roles at ProPharma are personally reviewed by a member of our recruitment team. We do not rely on AI screening tools to support our hiring process. You will always receive an outcome to your application so that you have an answer from us - whether you're successful or not. Whilst ProPharma supports remote working, we also recognise the value that comes from in person collaboration. As such, we encourage any new hires that are based within a reasonably short commute of one of our offices to work on a hybrid basis and spend some time working from that office location, as agreed with your manager. All applications will be treated on their own merit and candidates will not be at any advantage or disadvantage based on their proximity to an office.

Title: Senior Clinical Research Associate Location: Melbourne Australia Part time Job requisition id JR 9344 Job Description: For the past 20 years, ProPharma has improved the health and wellness of patients by providing advice and expertise that empowers biotech, med device, and pharmaceutical organizations of all sizes to confidently advance scientific breakthroughs and introduce new therapies. ProPharma partners with its clients through an advise-build-operate model across the complete product lifecycle. With deep domain expertise in regulatory sciences, clinical research solutions, quality & compliance, pharmacovigilance, medical information, and R&D technology, ProPharma offers an end-to-end suite of fully customizable consulting solutions that de-risk and accelerate our partners' most high-profile drug and device programs. About the Role We are seeking a motivated and detail-oriented Clinical Research Associate (CRA) to join our team on a 0.2 FTE (one day per week equivalent) basis. This is an excellent opportunity for an experienced CRA looking for flexible, part-time work while contributing to high-quality clinical research projects. Key Responsibilities - Conduct site monitoring visits (remote and on-site as required) in accordance with study protocols, ICH-GCP, and regulatory requirements - Ensure data integrity and compliance through source data verification (SDV) - Build and maintain strong relationships with investigational sites - Support site initiation, monitoring, and close-out activities - Identify and escalate risks or issues impacting study delivery - Assist with regulatory document review and maintenance of Trial Master Files (TMF) - Collaborate with cross-functional teams to ensure smooth study execution About You - Previous experience as a Clinical Research Associate (or similar role) - Strong understanding of ICH-GCP guidelines and clinical trial processes - Excellent communication and organisational skills - Ability to work independently with minimal supervision - Located in NSW or Melbourne, with willingness to travel occasionally if required - Relevant degree in life sciences, nursing, or a related field preferred We celebrate our differences and strive to create a workplace where each person can be their authentic self. We are committed to diversity, equity, and inclusion. Employees are encouraged to unleash their innovative, collaborative, and entrepreneurial spirits. With a holistic approach as an Equal Opportunity Employer, we provide a safe space where all employees feel empowered to succeed. All applications to roles at ProPharma are personally reviewed by a member of our recruitment team. We do not rely on AI screening tools to support our hiring process. You will always receive an outcome to your application so that you have an answer from us - whether you're successful or not. Whilst ProPharma supports remote working, we also recognise the value that comes from in person collaboration. As such, we encourage any new hires that are based within a reasonably short commute of one of our offices to work on a hybrid basis and spend some time working from that office location, as agreed with your manager. All applications will be treated on their own merit and candidates will not be at any advantage or disadvantage based on their proximity to an office. - ProPharma Group does not accept unsolicited resumes from recruiters/third parties. Please, no phone calls or emails to anyone regarding this posting.*

Title: Director, Regulatory Sciences Location: Washington DC Job Description: For the past 20 years, ProPharma has improved the health and wellness of patients by providing advice and expertise that empowers biotech, med device, and pharmaceutical organizations of all sizes to confidently advance scientific breakthroughs and introduce new therapies. ProPharma partners with its clients through an advise-build-operate model across the complete product lifecycle. With deep domain expertise in regulatory sciences, clinical research solutions, quality & compliance, pharmacovigilance, medical information, and R&D technology, ProPharma offers an end-to-end suite of fully customizable consulting solutions that de-risk and accelerate our partners’ most high-profile drug and device programs. The Director, Regulatory Sciences will be responsible for leading and overseeing projects for US Regulatory science clients, managing a team of professionals, and ensuring the successful delivery of regulatory strategies, submissions, and other deliverables. Expertise in regulatory affairs, pharmaceutical industry knowledge, and leadership skills will be crucial in driving the organization's strategy and achieving business objectives. Essential Functions - Develop and implement the overall strategy for regulatory submissions, approvals, and maintenance, aligned with the organization's goals and regulatory requirements. - Lead and mentor a team of regulatory professionals, providing guidance, support, and training to ensure high performance and professional development. - Stay updated on relevant regulations, guidelines, and industry trends, ensuring compliance and providing guidance to the team and stakeholders. - Oversee the preparation, review, and timely submission of high-quality client deliverables, including managing interactions with regulatory authorities. - Collaborate with cross-functional teams, including Research and Development, Manufacturing, Quality Assurance, and Legal, to ensure successful regulatory submissions within the defined timelines. - Ensure robust quality oversight for regulatory submissions, ensuring adherence to regulatory requirements and best practices. - Establish and maintain effective relationships with regulatory authorities, consultants, contract research organizations (CROs), and other external partners to support regulatory activities. - Provide input as requested into the department's budget, optimizing resource allocation and ensuring cost-effectiveness. - Identify and mitigate risks associated with deliverables and submissions, proactively addressing challenges and proposing solutions. - Other duties as assigned. Necessary Skills and Abilities: - Strong leadership skills, with experience managing and developing high-performance teams. - Excellent written and verbal communication skills, with the ability to effectively interact with internal stakeholders, regulatory authorities, and external partners. - Strategic mindset, with the ability to analyze complex regulatory issues and provide innovative solutions. - Strong project management and organizational skills, with the ability to prioritize and manage multiple tasks simultaneously. Educational Requirements: - Bachelor's degree in a relevant scientific discipline, advance degree preferred. Experience Requirements: - A minimum of 7 years of experience in regulatory affairs within the pharmaceutical industry, with a focus on regulatory strategic and operational leadership knowledge. - In-depth knowledge of FDA regulations, guidelines, and requirements, including Hatch-Waxman Act and other relevant legislation. - Proven track record of successful regulatory submissions and approvals, with a through understanding of the regulatory processes and requirements. We celebrate our differences and strive to create a workplace where each person can be their authentic self. We are committed to diversity, equity, and inclusion. Employees are encouraged to unleash their innovative, collaborative, and entrepreneurial spirits. With a holistic approach as an Equal Opportunity Employer, we provide a safe space where all employees feel empowered to succeed. All applications to roles at ProPharma are personally reviewed by a member of our recruitment team. We do not rely on AI screening tools to support our hiring process. You will always receive an outcome to your application so that you have an answer from us - whether you're successful or not. Whilst ProPharma supports remote working, we also recognise the value that comes from in person collaboration. As such, we encourage any new hires that are based within a reasonably short commute of one of our offices to work on a hybrid basis and spend some time working from that office location, as agreed with your manager. All applications will be treated on their own merit and candidates will not be at any advantage or disadvantage based on their proximity to an office. ***ProPharma Group does not accept unsolicited resumes from recruiters/third parties. Please, no phone calls or emails to anyone regarding this posting.***

Title: Information Specialist Location: United States Job Description: For the past 20 years, ProPharma has improved the health and wellness of patients by providing advice and expertise that empowers biotech, med device, and pharmaceutical organizations of all sizes to confidently advance scientific breakthroughs and introduce new therapies. ProPharma partners with its clients through an advise-build-operate model across the complete product lifecycle. With deep domain expertise in regulatory sciences, clinical research solutions, quality & compliance, pharmacovigilance, medical information, and R&D technology, ProPharma offers an end-to-end suite of fully customizable consulting solutions that de-risk and accelerate our partners’ most high-profile drug and device programs. Perform intake of health and safety calls, provide product safety information to consumers, end users and health care professionals and escalate calls to other staff or on-duty toxicologist as outlined in notification guidelines. Record complete and accurate documentation of health and safety calls in safety database. Maintain distinctive quality and commitment as the operating philosophy in carrying out all processes. Continually seek out ways to enhance customer service experience both internally and externally. Essential Functions Include: • Answer the telephone at the Health and Safety Call Center. • Handle calls involving both animals and humans. • Obtain demographic data on callers. • Document adverse event and information calls for manufacturers. • Follow up with callers to assure there are no further health concerns. • Determine if a call involves a product or a situation that requires escalation. • Escalate calls to other staff as appropriate. • Discuss health and safety concerns with consumers, workers, and health care professionals. • Respond with appropriate first-aid information based on client specifications without providing caller specific diagnostic or treatment advice. • Notify Lead Toxicologist about cases as outlined in the notification guidelines. • Watch for trends involving new products or new issues with existing products. • Stay up to date on continuing education requirements. • Other duties as assigned. Qualified candidates must have: • Required: EMT, Paramedic, Veterinary Technician, or equivalent or student working towards advanced medical degree. • Preferred: Current license or certification appropriate with degree. • Basic computer knowledge and computer keyboarding skills. • Professional telephone etiquette; active listening and pleasant speaking voice. • Able to translate complex medical information to consumers and health care professionals. • Excellent internal and external customer service skills. • Strong verbal, written and interpersonal communication skills. • Strong organization and prioritization skills; with strong attention to detail. • Ability to work well independently and within a team environment. • Able to work rotating schedule primarily second shift (US), rotating weekends and some holidays. #LI-KP1 #LI-REMOTE We celebrate our differences and strive to create a workplace where each person can be their authentic self. We are committed to diversity, equity, and inclusion. Employees are encouraged to unleash their innovative, collaborative, and entrepreneurial spirits. With a holistic approach as an Equal Opportunity Employer, we provide a safe space where all employees feel empowered to succeed. All applications to roles at ProPharma are personally reviewed by a member of our recruitment team. We do not rely on AI screening tools to support our hiring process. You will always receive an outcome to your application so that you have an answer from us - whether you're successful or not. Whilst ProPharma supports remote working, we also recognise the value that comes from in person collaboration. As such, we encourage any new hires that are based within a reasonably short commute of one of our offices to work on a hybrid basis and spend some time working from that office location, as agreed with your manager. All applications will be treated on their own merit and candidates will not be at any advantage or disadvantage based on their proximity to an office.

Title: Instrument Connectivity and Qualification Engineer (Consultant) Location: United States Job Description: time type Full time job requisition id JR 9505 For the past 20 years, ProPharma has improved the health and wellness of patients by providing advice and expertise that empowers biotech, med device, and pharmaceutical organizations of all sizes to confidently advance scientific breakthroughs and introduce new therapies. ProPharma partners with its clients through an advise-build-operate model across the complete product lifecycle. With deep domain expertise in regulatory sciences, clinical research solutions, quality & compliance, pharmacovigilance, medical information, and R&D technology, ProPharma offers an end-to-end suite of fully customizable consulting solutions that de-risk and accelerate our partners’ most high-profile drug and device programs. - Develop and maintain a tracking log (e.g., Excel, Smartsheet) of site-specific documentation required to enable instrument connectivity for all instruments in scope for LabVantage (e.g., URS, IQ, OQ, IVI, and related deliverables). - Complete LabVantage instrument registration in accordance with site procedures and project standards. - Provide additional support, as required and commensurate with experience, to prepare and/or execute instrument qualification and/or CSV deliverables We celebrate our differences and strive to create a workplace where each person can be their authentic self. We are committed to diversity, equity, and inclusion. Employees are encouraged to unleash their innovative, collaborative, and entrepreneurial spirits. With a holistic approach as an Equal Opportunity Employer, we provide a safe space where all employees feel empowered to succeed. All applications to roles at ProPharma are personally reviewed by a member of our recruitment team. We do not rely on AI screening tools to support our hiring process. You will always receive an outcome to your application so that you have an answer from us - whether you're successful or not. Whilst ProPharma supports remote working, we also recognise the value that comes from in person collaboration. As such, we encourage any new hires that are based within a reasonably short commute of one of our offices to work on a hybrid basis and spend some time working from that office location, as agreed with your manager. All applications will be treated on their own merit and candidates will not be at any advantage or disadvantage based on their proximity to an office. ***ProPharma Group does not accept unsolicited resumes from recruiters/third parties. Please, no phone calls or emails to anyone regarding this posting.***

Support pharmacovigilance activities by authoring aggregate safety reports, preparing Risk Management Plans, conducting literature searches, and ensuring compliance with global regulatory requirements while maintaining high-quality standards.

Title: IT .Net Programmer Location: Belgrade Job Description: time type Full time job requisition id JR 9254 For the past 20 years, ProPharma has improved the health and wellness of patients by providing advice and expertise that empowers biotech, med device, and pharmaceutical organizations of all sizes to confidently advance scientific breakthroughs and introduce new therapies. ProPharma partners with its clients through an advise-build-operate model across the complete product lifecycle. With deep domain expertise in regulatory sciences, clinical research solutions, quality & compliance, pharmacovigilance, medical information, and R&D technology, ProPharma offers an end-to-end suite of fully customizable consulting solutions that de-risk and accelerate our partners’ most high-profile drug and device programs. The IT Net Programmer is responsible for supporting, maintaining, and extending existing .NET applications that are critical to business operations. This role focuses on enhancing application functionality, improving performance and reliability, and ensuring seamless operation within an AWS-hosted environment. The .NET Developer will collaborate closely with cross-functional teams to deliver high-quality, scalable solutions while following established development standards and best practices. Job details - Maintain, support, and enhance existing .NET applications to meet evolving business needs. - Develop new features and functionality using .NET Framework/.NET Core, and related technologies. - Troubleshoot, diagnose, and resolve application defects and performance issues. - Collaborate with business stakeholders and technical teams to gather and refine requirements. - Design and implement scalable, secure solutions within an AWS-hosted environment. - Deploy, monitor, and support applications running on AWS services such as EC2, RDS, S3, and related infrastructure. - Optimize application performance, reliability, and maintainability. - Participate in code reviews and ensure adherence to development standards and best practices. - Develop and maintain APIs, integrations, and data access components. - Write and maintain unit tests and support quality assurance efforts. - Support CI/CD pipelines and automated deployment processes. - Create and maintain technical documentation for applications, processes, and enhancements. Requirements - Strong proficiency in C# and .NET Framework and/or .NET Core. - Experience supporting and enhancing existing enterprise .NET applications. - Solid understanding of object-oriented design principles and software development best practices. - Experience developing and consuming RESTful APIs and web services. - Familiarity with relational databases and data access technologies (e.g., SQL Server, Entity Framework). - Experience working with applications hosted in AWS environments. - Working knowledge of AWS services such as EC2, RDS, S3, and related infrastructure components. - Understanding of application security principles and secure coding practices. - Experience with source control systems (e.g., Git) and collaborative development workflows. - Familiarity with CI/CD pipelines and automated deployment processes. - Strong troubleshooting, debugging, and problem-solving skills - Ability to analyze existing codebases and implement enhancements with minimal disruption. - Strong written and verbal communication skills. - Ability to work independently as well as collaboratively in a team environment. - Required: Associate degree (2-year degree). - Preferred: BS / BA in Computer Science, Information Technology Certification. - Minimum three years’ experience in technician or similar applicable role We celebrate our differences and strive to create a workplace where each person can be their authentic self. We are committed to diversity, equity, and inclusion. Employees are encouraged to unleash their innovative, collaborative, and entrepreneurial spirits. With a holistic approach as an Equal Opportunity Employer, we provide a safe space where all employees feel empowered to succeed. All applications to roles at ProPharma are personally reviewed by a member of our recruitment team. We do not rely on AI screening tools to support our hiring process. You will always receive an outcome to your application so that you have an answer from us - whether you're successful or not. Whilst ProPharma supports remote working, we also recognise the value that comes from in person collaboration. As such, we encourage any new hires that are based within a reasonably short commute of one of our offices to work on a hybrid basis and spend some time working from that office location, as agreed with your manager. All applications will be treated on their own merit and candidates will not be at any advantage or disadvantage based on their proximity to an office. ***ProPharma Group does not accept unsolicited resumes from recruiters/third parties. Please, no phone calls or emails to anyone regarding this posting.***