Accountable for end-to-end study management activities (startup through database release), providing leadership for recruitment, monitoring, vendor oversight and inspection readiness. Requires advanced clinical research/study management experience, proven CRO/vendor oversight, budgeting and familiarity with GCP; fluency in English and ability to travel as required.

Accountable for country and regional study operational delivery from startup through close, including site activation, recruitment strategy, CRO and vendor oversight, regulatory/ethics submission coordination, quality and risk management, and escalation resolution. Requires a scientific/technical degree and 3–5 years relevant operational clinical trial experience depending on degree.

The Global Study Manager II provides operational leadership and accountability for study management deliverables across the study lifecycle, including study start-up, monitoring, vendor/pCRO oversight, budgeting, TMF management, and inspection readiness. Role requires fluency in English, experience in clinical research/study management (6–7+ years depending on degree), ability to travel as required, and supports remote work in Argentina, Brazil, and Mexico.

Parexel seeks a Senior Project Leader for Real-World Evidence (RWE) clinical trials to lead global study teams and manage day-to-day operations, scheduling, resources and budgets. Candidate should have 3+ years leading global clinical trials (CRO/Biotech/Pharma preferred), experience with regulatory submissions, strong problem solving, organizational and interpersonal skills. Role is homebased in the United States.

Accountable for global execution of site activation and country start-up strategy for assigned clinical trials. Responsibilities include developing site start-up strategy, CRO and vendor oversight, regulatory submission support, TMF/CTMS documentation, metrics tracking, risk mitigation, and cross-functional leadership. Role may require up to 25% travel and requires 4+ years' relevant experience.

Experienced regulatory project manager role supporting Global Regulatory Leads to develop and execute globally aligned regulatory strategies and plans (IND/BLA/MAA), manage submission readiness (eCTD, Veeva RIM), facilitate Global Regulatory Subteam (GRST) meetings, and drive cross-functional alignment. Requires a scientific/healthcare degree, minimum 7 years industry experience (≥5 years in regulatory or regulatory program management), hands-on submission experience, and strong project management and communication skills.

Responsible for planning and managing UAT deliverables, creating and executing test scenarios/scripts, coordinating testers and vendors, and ensuring validated eClinical systems meet sponsor and regulatory expectations. Requires 5+ years in clinical research/CRO or related settings, experience with clinical trial systems configuration/validation, and fluency in English.

Parexel is hiring a Senior Project Leader to manage medium-to-high complexity clinical trials remotely from India. The role requires 10+ years in clinical research or regulated environments, strong project management and strategic skills, knowledge of ICH-GCP and standard clinical systems (CTMS, EDC, IXRS, TMF), and responsibilities include project planning, budget and risk management, client relationship ownership, team leadership, and external representation.

Parexel seeks Project Leader and Senior Project Leader candidates for its Biotech division to lead global clinical trials (including Respiratory). Responsibilities include leading project teams, managing day-to-day operations, project scheduling, resource and budget management, coordinating team activities, and supporting the full clinical development process through regulatory submissions. Requires an undergraduate degree in a clinical/health field (advanced degree preferred) and at least 2 years' experience leading global clinical trials (CRO, biotech or pharma preferred). Role is home-based in the United States.

Parexel is hiring project management professionals for its Biotech Division to lead global clinical trials in Neurology, Psychiatry and Rare Disease. Roles include Project Leader, Senior Project Leader and Project Director; candidates should have a minimum of 2+ years leading global clinical trials (CRO/biotech/pharma preferred) and experience in scheduling, resource and budget management, team coordination and regulatory submissions.

Parexel seeks Project Leader and Senior Project Leader (and higher) candidates to lead global clinical trials for biotech clients across multiple therapeutic areas (including Neurology, Oncology/Hematology, Respiratory, Cardio, General Medicine and GLP-1/Obesity). Requires at least 2+ years leading global clinical trials in a CRO, Biotech or Pharma, experience with 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 lead Metabolic / GLP-1 / Obesity global clinical studies. Roles involve leading project teams, managing day-to-day operations, project scheduling, resources and budgets, coordinating team activities, and supporting the full clinical development process through regulatory submissions. Minimum requirement: undergraduate degree in a clinical/health field (advanced degree preferred) and at least 2 years' experience leading global clinical trials in a CRO, biotech, or pharma setting.

Parexel is hiring a Site Contract Leader to act as primary sponsor interface and lead end‑to‑end site contracting strategy and execution for global clinical trials. The role includes negotiating contracts, developing and assessing investigator budgets (not template‑driven), guiding project site contracts teams, managing timelines and budgets, and ensuring alignment to protocol and study objectives. Requires 3+ years in site contracting or a closely related CRO role and advanced MS Excel skills.

Deliver medical support and medical monitoring activities for clinical studies (including medical review of data, safety/serious adverse event review, medical input to PV workflows and regulatory safety reporting). Participate in study planning, protocol and study document development, training of study teams, audits/inspections, rotas for emergency medical contact, client engagement and support business development/proposal activities. Requires medical qualification, clinical practice experience, knowledge of GCP/ICH/FDA/EMEA guidelines and a minimum of 3 years' medical monitoring or medical data review experience.

Manage early-phase clinical studies from pre-award/bid defense and start-up through implementation and close-out. Own sponsor communications, lead kick-offs, oversee site selection, IRB/EC and RA processes, monitor timelines, recruitment and data cleaning, track budgets via CTMS, prepare for audits, identify and mitigate risks, and provide oversight and training to junior project staff. Requires a science-related bachelor's (advanced degree preferred) and 2 years' PM experience with Parexel or 3–5 years in related fields; knowledge of ICH-GCP and proficiency in MS Office.

Parexel seeks Project Leader and Senior Project Leader candidates to lead global biotech clinical trials (Oncology/Hematology, Respiratory/General Medicine, Obesity/Endocrine). Responsibilities include providing leadership to project teams, managing day-to-day operations, scheduling, resources and budgets, coordinating team activities, and supporting the full clinical development process through regulatory submissions. Undergraduate degree in a clinical/health field required (advanced degree preferred); minimum 2+ years' experience leading global clinical trials in a CRO, biotech, or pharma environment.

Responsible for end-to-end CTA project management across EU CTR and Rest of World, ensuring timely, compliant submissions through project management, regulatory expertise, risk/issue management, cross-functional collaboration and stakeholder engagement. Requires a bachelor’s in life sciences/pharmacy and minimum 5+ years industry experience.

The LSAD is responsible for leading Local Study Team(s) at country level to ensure timely delivery of clinical study commitments per ICH-GCP and client procedures. Duties include site identification/qualification, monitoring oversight, CTMS/eTMF management, regulatory and ethics submissions, budgeting and payments, risk management, and supporting audits/inspections. Role requires oncology experience, minimum 3 years in development operations or related fields, proficiency in English, a relevant bachelor's degree, and ability to travel nationally and internationally.

Role involves leading the site contracting lifecycle (strategy, execution, monitoring, risk mitigation), mentoring a site contracts team, collaborating with sponsors, CROs and internal stakeholders, managing budgets and forecasting, and developing project setup documents. Requires 3–5 years' experience in site contracting within the CRO industry and a bachelor's degree or equivalent.

Parexel seeks Project Leader and Senior Project Leader candidates to lead global clinical trials (biotech) in dermatology and other therapeutic areas. Responsibilities include leading project teams, managing day-to-day operations, project scheduling, resource and budget management, coordinating team activities and supporting the full clinical development process through regulatory submissions. Minimum requirement: undergraduate degree in a clinical/health field (advanced degree preferred) and at least 2+ years leading global clinical trials in project management within CRO/biotech/pharma.