Parexel seeks a Clinical Coding Manager to lead medical coding activities, manage coding dictionaries (MedDRA, WHODrug), review coded clinical data, support regulatory and pharmacovigilance interactions, and implement coding standards and process improvements. Requires a Bachelor's degree (Nursing/Biology or related) and 7 years' clinical coding experience, with experience in clinical research and relevant regulatory guidelines (ICH-GCP).

Parexel is hiring a Manager, Central Monitoring (home-based, Poland/Serbia) to lead central monitoring activities, author central monitoring plans, analyze KRIs/KPIs using analytical tools (CluePoints preferred), present findings to study teams, and support RBQM. Requires at least 7 years' relevant industry experience (minimum 1 year direct central monitoring) and may require ~25% travel. Compensation range for Poland: 300,000–320,000 PLN gross/year.

Experienced Senior CRA role based in the UK (ideally South West England) responsible for leading site preparation, initiation, routine/on-site/remote monitoring, source data review and site close-out. The role requires strong site management, stakeholder engagement, use of CTMS/eTMF and other clinical systems, management of drug accountability and reporting of serious adverse events, and support for audits/inspections. Proficiency in English and ability to travel nationally and internationally are required.

Parexel seeks a Senior Salesforce Functional Analyst to translate business needs into requirements, configure Sales Cloud declaratively, and design/execute system, integration, and regression tests (including automated testing). Requires 5+ years hands-on Salesforce experience, Salesforce Administrator certification, familiarity with APIs, Agile/Jira, and support for shift hours and weekend releases.

Parexel is hiring a Senior Salesforce Functional Analyst to translate business needs into Salesforce solutions, lead requirements gathering and solution design, configure declarative Salesforce features, support UAT, manage stakeholder communication, and drive process improvements. Role requires 5+ years hands-on Salesforce experience, Salesforce Administrator certification, experience with Sales Cloud and Service Cloud, familiarity with Agile/Jira/Visio, and ability to work shift hours (IST).

Join Parexel as a Senior Salesforce Developer to design and implement declarative and programmatic solutions on Sales Cloud, Service Cloud, Marketing Cloud (Pardot) and AppExchange/CLM tools. Role includes building API integrations (REST, SOAP, Bulk), leading code quality, supporting releases and production operations, mentoring junior developers, and working in Agile teams. Requires 5+ years hands-on Salesforce experience and Salesforce Administrator, Platform App Builder, and Platform Developer I certifications; healthcare/clinical development experience is preferred.

Parexel seeks a Senior Market Development Analyst to research target accounts, therapeutic areas, and competitive activity; identify high-potential prospects and white-space; maintain Salesforce data; develop reports and dashboards; and support targeted outreach to generate qualified meetings. Requires 3–5 years in market development, BD analytics, or related commercial roles and experience with CRM/market intelligence tools.

Parexel seeks a medically qualified Medical Director with specialist training and clinical experience in Rheumatology to act as Global or Regional Lead Physician and Medical Monitor for rheumatology clinical studies. Responsibilities include medical monitoring, medical review of study documents, pharmacovigilance input, study planning, client engagement and supporting business development. Excellent written and spoken English and up-to-date rheumatology knowledge are required.

Parexel is hiring a remote Manager, Patient Safety (also described as Pharmacovigilance/Drug Safety Operations Manager). The role manages and develops patient safety staff, oversees ICSR processing, signal and risk management, safety medical writing, and compliance with ICH/CIOMS/GVP and company SOPs. Responsibilities include KPI/SLA management, client communication, resource and budget forecasting, audit/inspection support, and driving adoption of automation and digital solutions in pharmacovigilance.

Parexel is hiring Clinical Research Associate II to act as primary site contact and manager across study phases, performing remote and onsite monitoring, managing regulatory documentation, and supporting audits. Requires a minimum of 2 years direct site monitoring experience, strong GCP/ICH knowledge, IT skills (CTMS/eTMF/MS Office), and willingness to travel extensively (approx. 65–75%).

Provide CMC regulatory strategy and expertise for biologic and small-molecule products across development and post-approval, prepare and review CMC/GMP submission documents (IND/NDA/DMF), support health authority CMC meetings, and collaborate with manufacturing, quality, technical operations, affiliates, and external partners. Requires 4–6 years CMC experience.

Provide strategic leadership for CMC aspects of late-stage and marketed vaccine products, lead complex regulatory submissions (IND, IMPD, BLA, MAA), manage health authority interactions, oversee manufacturing change regulatory assessments, and collaborate with senior R&D, Manufacturing, Quality and Clinical teams. Requires an advanced degree and a minimum of 10 years' Regulatory Affairs experience with strong CMC focus.

Senior leadership role within Parexel HEOR Consulting (remote, US) accountable for service-line performance and financial outcomes; leads HEOR modeling and AI initiatives, client engagements, business development, project delivery, and team development. Requires a Bachelor's degree, 15+ years' experience and 10+ years management experience; fluent English.

Parexel FSP is hiring a Manager, Central Monitoring to lead central monitoring activities for global/complex trials, including authoring the Central Monitoring Plan, performing analytical reviews of KRIs/KPIs, presenting findings to study teams, tracking actions, and partnering with CROs. Role requires strong data analytics and Excel skills, experience with clinical databases/EDC, knowledge of ICH/GCP, and at least 7 years of relevant biotech/pharma experience (including ≥1 year direct central monitoring). CluePoints experience is preferred.

Parexel seeks a Solutions Consultant – Logistics to develop and support competitive, operationally achievable clinical logistics solutions across the pre-sales and post-award lifecycle. The role requires clinical trial logistics expertise, collaboration with cross-functional teams, proposal and solution development, risk assessment, and up to 30% travel. Location: remote in Brazil or Argentina.

Parexel is hiring a home-based Proposals and Contracts Manager (Romania, Ireland, Spain, or UK) to lead RFP and proposal processes, prepare and negotiate contracts, coordinate SMEs and internal stakeholders, manage budgets and risks, and deliver client agreements in line with SOPs. Role requires experience in proposals or contracting within CRO/life sciences environments and strong negotiation, organizational, and communication skills.

Parexel is hiring a SKDL Programming Lead (home-based in Spain) to manage biosample planning and execution, sample and kit logistics, and programming/support for laboratory operations. The role requires minimum 6 years clinical research experience and proficiency in programming (Python, R, MATLAB, SQL, Perl), database/dashboard development, LIMS and clinical trial data processes, with responsibilities spanning vendor management, data transfer specifications, and compliance with clinical/regulatory standards.

Parexel seeks a home-based, sponsor-dedicated Precision Medicine Operations Lead / SKDL Programming Lead in Poland to support sample management, biosample logistics, specialty laboratory databases, and programming for supplies and laboratory operations. Responsibilities include study team support, operational planning for biosamples, data transfer/specifications, LIMS and kit inventory oversight, and development of tools/dashboards. Requires minimum 6 years clinical research experience, fluency in English, and strong technical skills (Python/R/MATLAB/SQL, APIs, Linux/Unix), plus experience with clinical trial operational data (EDC, lab/vendor datasets).

Lead role supporting precision medicine across global clinical studies, responsible for oversight of biomarker samples, kits, laboratory operations, logistics and associated data. Requires minimum 6 years clinical research experience, proficiency in programming (Python, R, Perl, SQL), familiarity with LIMS and laboratory databases, and fluent English.

The SrCRA supports monitoring and site management for client-sponsored early development studies, performing on-site and remote qualification, initiation, interim and close-out visits; overseeing CRO CRAs through review of metrics and oversight monitoring visits; ensuring compliance with protocol, ICH GCP and local regulations; maintaining site regulatory files and preparing monitoring reports. Requires a bachelor’s degree (or equivalent), minimum 5 years related experience, working knowledge of clinical drug development and ICH GCP, and proficiency with EDC, CTMS and Microsoft Office.