Remote Jobs at Parexel
Find your next remote opportunity · 69 Open Positions
Parexel is among the world’s largest clinical research organizations (CROs), providing the full range of Phase I to IV clinical development services to help life-saving treatments reach patients faster.
Leveraging the breadth of our clinical, regulatory and therapeutic expertise, our team of more than 21,000 global professionals collaborates with biopharmaceutical leaders, emerging innovators and sites to design and deliver clinical trials with patients in mind, increasing access and participation to make clinical research a care option for anyone, anywhere.
Our depth of industry knowledge and strong track record gained over the past 40 years is moving the industry forward and advancing clinical research in healthcare’s most complex areas, while our innovation ecosystem offers the best solutions to make every phase of the clinical trial process more efficient.
With the people, insight and focus on operational excellence, we work With HeartTM every day to treat patients with dignity and continuously learn from their experiences, so every trial makes a difference.
For more information, visit parexel.com.
Community Guidelines
Because Parexel’s social media channels are open to the general public and employees, we are not responsible for views expressed other than our own.
However, we do not tolerate posts that are:
• Abusive, harassing or threatening to others.
• Defamatory, offensive, obscene, vulgar or depicting violence.
• Hateful targeting by race/ethnicity, age, color, creed, religion, gender,
sexual preference or orientation, nationality or political beliefs.
• Sexually explicit or pornographic.
• Fraudulent, deceptive, libelous, misleading or unlawful.
• Referencing criminal or illegal activity.
• Spamming.
We reserve the right to remove any comments that do not adhere to our guidelines as well as report users who violate the rules of our page.
Early Clinical Scientist – Translational Medicine
Early Clinical Scientist coordinating early-phase clinical trials for Parexel’s clinical development services. Overseeing safety, data validity, CRO performance, and trial documentation.
Clinical Study Team Associate II – FSP
Clinical Study Team Associate supporting Parexel’s global clinical trials across Argentina, Brazil, and Mexico. Managing study operations, documentation, systems, timelines, and compliance.
Clinical Study Team Assistant II – FSP
Clinical Study Team Assistant supporting Parexel’s LATAM clinical trials from study start-up through close-out. Managing trial systems, documentation, metrics, budgets, timelines, and team coordination remotely.
Site Care Partner – Oncology
Site Care Partner supporting UK oncology clinical trials for Parexel, a global clinical development partner. Managing investigator sites from start-up through closeout while ensuring compliance and recruitment performance.
Study Grant Analyst II
Study Grant Analyst II preparing compliant clinical trial budgets and analyses for Parexel’s clinical development services. Managing grant estimates, fair-market-value compliance, and client-focused proposal support.
Supply and Logistics Specialist
Supply and Logistics Specialist managing clinical trial supply chains at Parexel. Developing sourcing, distribution, inventory, and logistics strategies for compliant clinical development projects.
Senior Statistical Programmer, SAS Programmer
Senior SAS Programmer supporting Parexel’s clinical trials through statistical programming, data analysis, and regulatory reporting. Leading global teams and ensuring quality, timelines, budgets, and compliance.
Data Surveillance Analyst
Data Surveillance Analyst analyzing clinical and operational data for Parexel’s clinical development solutions. Developing surveillance plans, identifying quality signals, and supporting global project teams.
Senior Clinical Data Engineer
Senior Clinical Data Engineer designing regulated data solutions for Parexel's clinical trials. Leading ingestion, validation, reporting, and technical teams in Hyderabad.
Data Surveillance Analyst
Data Surveillance Analyst supporting Parexel’s clinical development solutions through data surveillance, risk indicators, and central monitoring. Reviewing data quality signals and escalating study issues.
Clinical Research Associate, FSP
Clinical Research Associate monitoring sites, data, safety, and compliance for Parexel’s clinical development services. Supporting trial timelines, audits, issue resolution, and junior CRA mentoring.
Biometrics Delivery Lead
Biometrics Delivery Lead overseeing clinical-trial data operations, technology, and delivery for Parexel’s EMEA projects. Leading cross-functional teams, budgets, timelines, and client-facing execution.
Site Care Partner
Site Care Partner managing US investigative sites for Parexel’s clinical trial services. Supporting site activation, recruitment, quality, regulatory compliance, and study close-out.
Clinical Research Associate I/II/Senior
Clinical Research Associate monitoring investigator sites and clinical trial data for Parexel. Ensuring compliant, high-quality studies that advance therapies and improve global health.
Patient Safety Physician
Drug Safety Physician supporting Parexel’s global pharmacovigilance and clinical research programs. Reviewing adverse events, monitoring safety signals, and supporting regulatory compliance.
Clinical Research Associate II
Clinical Research Associate II monitoring investigator sites and clinical trial data for Parexel’s global healthcare solutions. Ensuring ICH/GCP compliance, patient safety, documentation, and study quality.
Clinical Research Associate II
Clinical Research Associate II monitoring investigator sites and clinical trial data for Parexel, a global clinical development services provider. Ensuring compliance, documentation, and patient safety.
Clinical Research Associate II
Clinical Research Associate II monitoring investigator sites and ensuring clinical-trial data quality for Parexel’s clinical development solutions. Managing site documentation, compliance, reporting, and patient safety.
Clinical Research Associate II
Clinical Research Associate II monitoring investigator sites and clinical trial data for Parexel, a global clinical development services company. Ensuring ICH/GCP compliance, documentation quality, and study progress.
Senior Regulatory Affairs Associate
Senior Regulatory Affairs Associate managing life-cycle regulatory submissions for Parexel’s clinical development solutions. Handling CMC authoring, health authority responses, variations, and post-approval updates across global markets.