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Location
Remote (India)
Seniority
Staff · 10+ years exp
Employment
Full-Time

Confirmed on the employer's own hiring board on Oct 12, 2026. First seen by Alion on Sep 25, 2026.

Overview
Company
Impact
Profile match
Parexel is a clinical research organisation headquartered in Durham, North Carolina that provides Phase I to IV clinical trial services, regulatory consulting, market access and safety services to biopharmaceutical companies. Founded in 1983 and owned by EQT and Goldman Sachs since 2021, it employs more than 21,000 people, with large teams in the US, Hyderabad, Bengaluru, London, Poland, Romania, Serbia and Bloemfontein. Its openings are mostly for regulatory affairs consultants and associates, clinical research associates, safety technology analysts, clinical trial managers, data and AI engineers, many of them home or office based.

When our values align, there's no limit to what we can achieve.

At Parexel, we all share the same goal - to improve the world's health. From clinical trials to regulatory, consulting, and market access, every clinical development solution we provide is underpinned by something special - a deep conviction in what we do.

Each of us, no matter what we do at Parexel, contributes to the development of a therapy that ultimately will benefit a patient. We take our work personally, we do it with empathy and we're committed to making a difference.

About Parexel

Parexel is a leading global clinical development partner delivering insights-driven clinical and consulting solutions to the life sciences industry. With 22,000+ employees worldwide, we partner with biopharmaceutical companies and research sites to design and deliver patient-focused clinical trials that broaden access and make research a care option for anyone, anywhere.

We work with focus, agility, and shared purpose -- moving with urgency to address patient needs and accelerate the delivery of new therapies. We embrace bold thinking, adapt quickly to change, and continually raise the bar for the speed and quality of clinical research. We are expanding our team and seeking talented individuals to help drive industry leading innovation, With Heart.

About the Role

We are seeking a Project Leader to join our team in a Remote capacity. As a Project Leader, you will lead Parexel and client teams by combining deep clinical research expertise with strategic insight to develop innovative solutions that drive clinical trial success. This position plays a key role in study execution, operational excellence, regulatory compliance, and client satisfaction. You'll collaborate with cross-functional teams, leverage industry-standard processes, and drive study outcomes from planning through closeout.

You'll join a fast-paced, growth-oriented environment focused on making a meaningful impact through strategic project leadership and advancing new treatments for patients. With diverse teams and continuous learning opportunities, the Project Leader can explore career paths and expand skills across clinical research and project management.

Key Responsibilities

  • Lead and manage medium to high complexity clinical trials or low complexity clinical trial programs with full accountability for project deliverables, timelines, budgets, and quality standards.
  • Develop and maintain comprehensive project plans with key milestones, budgets, and resources assigned to specific tasks and outcomes; define metrics for reporting performance against plan.
  • Own the client relationship at the study level, establishing effective communication channels and standards that ensure high client satisfaction and timely delivery of solutions.
  • Manage project profitability through budget oversight, revenue recognition, forecasting, resource management, and change in scope management in collaboration with cross-functional partners.
  • Identify and mitigate project risks, implement contingency plans, and keep clients informed of risks and mitigation strategies.
  • Establish quality standards that drive individual and team commitment to quality; monitor deliverables and implement corrective and preventative actions as needed.
  • Lead cross-functional project teams to achieve successful study completion; establish team goals, inspire ownership, and maintain accountability through regular project reviews.
  • Represent Project Leadership in external client meetings, bid pursuits, investigator meetings, and professional conferences.
  • Act as a role model and mentor for Project Leaders and junior staff; support program management responsibilities as needed.

You'll thrive in this role if you bring

  • Advanced project management and strategic thinking skills with the ability to create urgency and develop solutions-based approaches.
  • Excellent interpersonal, verbal, and written communication skills with strong conflict management abilities.
  • 10+ years of experience working in clinical research, healthcare, or in a regulated environment with proven success managing complex projects.
  • The ability to work independently with minimal oversight, analyze complex situations, and develop nonstandard solutions.
  • A patient-focused mindset, high accountability, and strong attention to detail in all deliverables.
  • Proficiency with Microsoft Office (Excel, PowerPoint, Word), project planning software, and standard clinical research systems (CTMS, EDC, IXRS, TMF).
  • Ability to thrive in a matrix environment, value teamwork, and embrace Parexel's High-Performance Culture principles.

Required Qualifications

  • Bachelor's degree in a science or medical-related field.
  • Proven advanced project management experience in healthcare, clinical research, or contract research organization.
  • Proven track record of developing and managing client relationships at the project level.
  • Knowledge of ICH-GCP, regulatory requirements, and clinical trial processes
  • Strong communication, organization, and problem-solving skills.

Preferred Qualifications

  • Advanced degree (Master's or higher) in a related field.
  • PMP or equivalent project management certification.
  • Experience managing different trial phases and program-level responsibilities.
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