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.About ParexelParexel is a leading global clinical development partner delivering insights-driven clinical and consulting solutions to the life sciences industry. With 22,000+ employees worldwide, we partner with biopharmaceutical companies and research sites to design and deliver patient-focused clinical trials that broaden access and make research a care option for anyone, anywhere.We work with focus, agility, and shared purpose - moving with urgency to address patient needs and accelerate the delivery of new therapies. We embrace bold thinking, adapt quickly to change, and continually raise the bar for the speed and quality of clinical research. We are expanding our team and seeking talented individuals to help drive industry leading innovation, With Heart.About the RoleIn this role, you will oversee all aspects of clinical trial delivery—from site identification and qualification through setup, monitoring, and closure—ensuring compliance with international guidelines (ICH-GCP) and local regulations.Key ResponsibilitiesLead and motivate Local Study Teams (CRAs, CSAs) to deliver clinical trials on time, within budget, and to the highest quality standardsManage site identification, qualification, setup, initiation, monitoring, and closure activitiesOversee and coordinate monitoring activities from site activation through study closure in accordance with monitoring plansEnsure compliance with Client Procedural Documents, ICH-GCP guidelines, and local regulationsDevelop and maintain risk management plans; proactively identify and resolve complex study issuesManage trial essential documents, including Informed Consent Forms (ICFs) and regulatory submissionsPrepare and maintain country-level financial Study Management Agreements and budgetsCoordinate with regulatory authorities, ethics committees, and national investigatorsContribute to patient recruitment strategy and maintain relationships with participating investigatorsPerform site monitoring as needed to support flexible capacity modelsWhat We're Looking ForEssential:Minimum 3 years of experience in Development Operations (CRA/SrCRA) or related clinical research fieldsProven ability to lead and motivate cross-functional teams to deliver results on time and within budgetExcellent project management, organizational, and communication skills (verbal and written)Strong knowledge of ICH-GCP guidelines and local regulationsBachelor's degree in life sciences or related disciplineExcellent attention to detail and ability to prioritize multiple tasksGood negotiation skills and ability to work effectively with IT systemsDesirable:Medical knowledge and understanding of drug development processesStrong analytical and financial management skillsExcellent understanding of clinical study processes, including monitoring and data managementGood intercultural awareness and change management experienceBasic coaching and crisis management skillsWhat We OfferOpportunity to lead dynamic teams in cutting-edge clinical researchProfessional development and career growth in a global organizationCompetitive compensation and comprehensive benefits packageCollaborative work environment with talented professionalsTravel opportunities (national and international as required)Apply now to make an impact on clinical trial delivery!SummaryLocation: United Kingdom-Harrow-Remote; United Kingdom-London-Gridiron-RemoteType: Full time
Local Study Associate Director - LSAD employer: PAREXEL
At Parexel, we pride ourselves on being an exceptional employer, offering a collaborative work culture that fosters innovation and professional growth. Our team members enjoy competitive benefits, including flexible working arrangements and opportunities for career advancement, all while contributing to impactful global clinical trials in a supportive environment across the UK, Poland, Serbia, and Hungary.
