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.

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 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.

Parexel is hiring Project Leader and Senior Project Leader roles (home-based, United States) to lead global clinical trials for biotech clients across therapeutic areas including neurology, oncology, respiratory, dermatology, cardiology and GLP-1/obesity. Requires at least 2 years' experience leading global clinical trials (project management within CRO/biotech/pharma preferred) and experience in project scheduling, resource and budget management, team coordination and the full clinical development process through regulatory submissions.

Parexel seeks Project Leader and Senior Project Leader candidates to provide leadership for global clinical trial projects across therapeutic areas. Roles are homebased (United States - Remote) and require a minimum of 2+ years' experience leading global clinical trials in project management within a CRO, biotech, or pharma, plus experience in project scheduling, resource and budget management, team coordination, and the clinical development process through regulatory submissions.

Parexel is hiring a Vendor Strategy Director / Project Director to define and execute program-level vendor strategies across clinical trials. The role partners with clinical program leads, procurement and cross-functional stakeholders to manage supplier performance, mitigate risks, support inspection readiness, enable early supplier engagement, and drive operational improvements. Requires 10+ years' industry experience and fluency in English.

Lead role responsible for sample management, biosample processing, data acquisition and programming (Python/R/SQL), LIMS and clinical trial logistics for precision medicine studies. Requires minimum 6 years clinical research experience and a bachelor's degree in life sciences or equivalent.

Programming Lead supporting sample management, biosample processing, kit logistics, LIMS and related data operations across the study lifecycle. Role includes collaborating with study teams, data management and biostatistics on data capture and transfer, vendor assessment and operational budgeting, and developing tools/dashboards and programming solutions (e.g., Python/R/SQL) to track samples, kits and laboratory data. Requires a minimum of 6 years clinical research experience and fluent English.

Responsible for coordinating clinical project teams on small to midsize studies, managing study start-up activities, monitoring timelines, patient recruitment and data cleaning, and resolving site issues. Ensures compliance with ICH-GCP, local regulations, and Parexel SOPs; prepares for audits/inspections and supports database lock, close-out, and archiving. Requires substantial clinical research experience (e.g., CRA), strong English communication, proficiency with Microsoft Office and WebEx, and ability to travel as required.

Parexel FSP seeks a Clinical Laboratory Study Manager based in Argentina to oversee biosample planning, storage, shipping, tracking, vendor management, and related data operations for precision medicine studies. The role partners with clinical, data management and biostatistics teams to develop sample-related protocol sections, manage LIMS and specialty lab databases, ensure regulatory compliance (ICH/GCP/US FDA), and may involve programming work (Python/R/SQL) and logistics oversight. Minimum 6 years clinical research experience and a life sciences bachelor degree or equivalent are required.

Responsible for managing site activation timelines and documentation, maintaining site relationships, ensuring regulatory and TMF compliance, supporting inspection readiness, and working cross-functionally to address regional challenges for sites in the US and Canada.

The Clinical Laboratory Study Manager supports precision medicine studies by managing biosample process planning (collection, storage, shipping, destruction), vendor selection and oversight, sample tracking and LIMS activities, and coordination with data management/biostatistics for data transfer and reporting. Requires a bachelor's degree (life sciences preferred) and a minimum of 6 years clinical research experience; programming skills (Python/R/Perl/SQL) and regulatory knowledge (ICH/GCP, FDA) are referenced when acting in programming or technical lead capacities.

Parexel is seeking a Contracts Manager to own the contract process for specific accounts, act as primary client contact during negotiations, create and finalize budgets and contractual documents (Start-up Agreements, Work Orders, Change Orders), maintain contractual records, and work closely with Operations, Project Management, Legal and Finance. Role can be home or office based in the UK or Ireland; fluency in English and experience in contract management or proposal development within clinical trials/life sciences is required or preferred.

Responsible for performance and compliance of assigned country protocols (ICH/GCP), executing and overseeing clinical trial submissions and approvals, managing budgets and contracts, coordinating local vendors/sites and mentoring Clinical Trial Coordinators. Requires bilingual English/French, 5+ years clinical research or combined experience, and the ability to work hybrid (office presence in Montreal/Kirkland ~2 days/week).

Parexel is seeking a Senior/Global Regulatory Labeling Strategist to define and lead global labeling strategy and execution (CCDS, TPL, regional labels, HA responses) across development and post-approval lifecycle. The role requires 7+ years industry experience with significant global labeling leadership, strong medical/technical writing skills, CTD experience, and familiarity with systems such as Veeva RIMS, eDMS, Docubridge, and Trackwise. The position is US-based remote with preference for candidates able to cover EST hours.

Parexel is hiring a remote Site Contracts Leader (based in Mexico or Argentina) to lead end-to-end site contracting strategy and execution for global clinical trials. Responsibilities include sponsor interface and calls across time zones, managing site contracts teams, investigator budget development and assessment, timeline and budget management, and navigating multinational contracting and regulatory requirements. Required: bachelor's degree or equivalent, 3–5 years in site contracting or related CRO role, advanced MS Excel, negotiation skills, and global trial experience.

Responsible for developing patient-focused, risk-informed feasibility and operational strategies for clinical trial proposals. Collaborates with RFP teams and stakeholders to produce data-driven country, site and enrolment recommendations, prepare compelling proposal text and presentations, and support pre-award feasibility activities and innovative pilots. Requires strong clinical/CRO experience, analytical skills, stakeholder communication and leadership within assigned therapy areas.