Parexel is hiring a Patient Recruitment Associate to support patient recruitment, engagement and retention initiatives for clinical trials. Responsibilities include coordinating patient-facing materials, working with vendors and study teams, monitoring KPIs and recruitment performance, supporting budgets and project documentation, and assisting client communications. Role is home-based in Argentina, Brazil or Mexico with flexible working arrangements; strong English and Microsoft Office skills are required.

Parexel is hiring a Site Care Partner/Lead CRA to act as liaison for investigative sites across a study lifecycle. Responsibilities include site selection, start-up and activation (ICF review, SIV), supporting monitoring and enrollment delivery, managing site relationships and operational quality, addressing escalated site issues, and ensuring compliance with GCP and regulatory requirements. Minimum ~5 years' experience and English required.

Parexel is seeking a Clinical Research Associate II for its Multi-Sponsor Clinical Trials Team in Poland (remote). The role includes conducting site qualification, initiation, monitoring and termination visits; ensuring patient safety, protocol and regulatory compliance; overseeing data quality and drug accountability; and supporting patient recruitment. Requires site management/clinical research experience, ability to perform monitoring independently, a bachelor’s degree in a life/health science, and proficiency with CTMS/EDMS and MS Office.

Parexel Clinical Research Associate II role involves conducting SDV, managing multiple investigator sites, ensuring patient safety and regulatory compliance (ICH-GCP and local regulations), maintaining site documentation (SMF, TMF/ELARA, IIP), generating monitoring reports, and training site staff. Requires proficiency in Chinese and good written/spoken English, a bachelor’s degree in a life science/nursing/pharmacy field, and at least ~1.5 years (2 years preferable) of clinical monitoring/site management experience.

Senior Regulatory Affairs role responsible for lifecycle management of approved drug products (small molecules and biologics including vaccines and monoclonal antibodies). Tasks include authoring and delivering CMC components of Marketing Authorization Applications and Variations, handling health authority queries, preparing post-approval CMC updates, performing regulatory impact assessments, and using RIMS (e.g., Veeva Vault). Experience with EU (DCP/MRP) and US procedures, GMP submissions, DMF and stability/specification reviews, and label authoring based on CCDS/PRAC/CMDh is required.

Role (Investigator Contract Lead, FSP) responsible for site contracting (CSA/CRC/ICD review & execution), site budget development aligned with Fair Market Value (FMV), basic legal/cost negotiation, and coordination with CTM/Legal/study teams. Requires legal background, preferably MS degree, strong communication/writing/PPT skills and more than 3 years' clinical trial site contracting experience.

The CRA will manage assigned investigator sites from activation through close-out, performing onsite and remote monitoring, ensuring protocol and regulatory compliance (ICH/GCP, FDA), supporting enrollment and SAE handling, maintaining TMF and study documentation, and partnering with the Site Care Partner and study team. Minimum 2 years monitoring experience, fluent English, and ability to travel 60–80% are required.

The Senior Clinical Research Associate will manage and monitor investigator sites from activation through close-out, ensuring compliance with GCP, ICH, FDA and Sponsor standards, safeguarding patient safety, and supporting enrollment and database release. Requires minimum 3 years of site monitoring experience (preferably 2 years in Oncology), a bachelor's or professional degree in life sciences (e.g., nursing, pharmacy), fluency in English, and a valid driver’s license and passport. Travel expectancy is 60–80%.

Senior commercial strategy leader to evaluate opportunities, lead bid pursuits (RFI/RFP), conduct market and competitive analysis, coach bid teams, and collaborate with sales, operations, and technical teams to shape Parexel's market positioning. Requires 15+ years in the CRO industry, global team leadership experience, proposal development expertise, and willingness to travel as needed.

Responsible for initiating and coordinating activities and essential document management to produce high-quality Investigator Initiation Packages and support site initiation. Role requires at least 2 years' clinical trials experience, knowledge of ICH/GCP and regulatory requirements (including FDA), maintenance of clinical trial systems, and fluent English; multi-language skills are an asset.

The Senior CRA will manage and monitor assigned investigator sites from activation through database lock, ensuring compliance with GCP, applicable regulations and sponsor standards. Key duties include onsite and remote monitoring, AE/SAE handling, TMF and site documentation, resolving protocol-related issues, supporting enrollment, training site staff, investigational product oversight, and driving audit/CAPA activities. Requires a bachelor's or professional degree in life sciences (or equivalent), minimum 3 years of site monitoring experience, fluency in English, frequent travel (60–80%), valid driver's license and passport.

The role requires strong expertise in CMC for biologicals (initial submissions and lifecycle maintenance), preparing CMC sections of IND/IMPDs, BLA/NDA/MAAs and post-approval variations, knowledge of ICH/EU/US regulations, experience with change management and document management systems (e.g., Veeva). A university degree in a pharmaceutical-related discipline and 10+ years' industry experience are required; fluent English is required.

Parexel seeks a Regulatory Affairs Consultant with a few years' experience in CRO/pharma and experience with Clinical Trial Applications (CTA) across Europe. The role involves preparing and compiling submission packages, authoring regulatory documentation, coordinating global submission activities, and working with study teams and health authorities. Requires a Bachelor's degree in a scientific/technical discipline, client-facing skills, strong interpersonal and intercultural communication, and proficiency in English and the local language.

Responsible for end-to-end operational oversight of global clinical studies: sourcing and vendor selection, study startup, monitoring and TMF management, budget and contract oversight, CRO/vendor management, inspection readiness, and mentoring Study Operational Managers. Requires clinical research/study management experience and advanced knowledge of study management processes and GCP.

Contract Senior Clinical Database Programmer (6-month fixed-term) supporting design, implementation, and maintenance of EDC and CDMS platforms in CDISC or standard formats. Responsibilities include creating edit/consistency checks, managing database lock/unlock, maintaining regulatory and technical documentation, integrating systems (e.g., CTMS, safety systems), mentoring programming teams, and supporting business development. Requires 6+ years' clinical data programming experience and familiarity with SAS, SQL, SDLC, ICH-GCP, and 21 CFR Part 11.

Parexel seeks a Senior Regulatory Affairs Associate to manage worldwide post-approval CMC regulatory activities for biologics and vaccines. Responsibilities include developing submission strategies, assessing change controls, reviewing QC/production reports, coordinating submission preparation across functions, writing/reviewing submission content, and maintaining regulatory information management systems. Role can be home- or office-based in specified European countries; fluency in English is required.

Parexel is hiring a Senior Clinical Site Contracts and Budgets Specialist (remote, Italy) to execute end-to-end site contracts and budgets processes, negotiate and maintain clinical agreements, ensure compliance with Fair Market Value and regulatory standards, collaborate with cross-functional stakeholders, and support contract lifecycle management and reporting. Requires a bachelor's degree (or equivalent) and 3+ years' relevant industry experience.

Parexel seeks a Site Monitoring Lead to plan and execute trial-level site monitoring strategies, oversee CRO-delivered site activities, perform risk assessments and trend analysis, support inspection readiness, and collaborate with global clinical teams to ensure compliance with protocols, ICH GCP, and regulatory requirements. The role requires several years of site monitoring/site management experience, strong stakeholder and training skills, and fluent English.

Parexel is hiring a Program Lead, FSP Operations (Data Management) to lead Data Management FSP programs. Responsibilities include strategic direction, financial management (budgeting, profitability, billing), workforce infrastructure and forecasting, quality and performance metrics, regulatory compliance, and stakeholder/client relationship management. Requires minimum 5+ years FSP Data Management leadership in a CRO and at least 3 years of line management experience.

Seeking a Senior Statistical Programmer (remote, India) to provide technical expertise for clinical study analysis and reporting. Responsibilities include development and QC of derived datasets, tables/listings/figures (TLFs), adherence to CDISC and regulatory standards (ICH-GCP, 21 CFR Part 11), creation of macros/process improvements, project coordination, and support for audits/inspections. Proficiency in SAS and experience in clinical trials are required; 5+ years end-to-end programming (SDTM/ADaM/TLFs) is listed as preferred.