Director, Global Clinical Operations Quality Management

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Hiring Remotely in Bengaluru, Bengaluru Urban, Karnataka, IND
In-Office or Remote
Pharmaceutical
The Role

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.

Strategic leadership of GCO Quality Management

  • Collaborate with GCO leadership to develop and implement the strategy and direction for the GCO QM team

  • Execute GCO QM mission and vision, including oversight of Global Support Centers

  • Propose, lead, and implement GCO QM initiatives aligned with GCO priorities

People leadership and development

  • Attract, recruit, retain, and develop qualified GCO QM staff

  • Ensure staff are appropriately trained, resourced, and deployed

  • Provide performance feedback, coaching, and succession planning

Quality issue management and oversight

  • Provide end-to-end oversight of quality issue management including triage, severity, categorization, RCA, and closure

  • Assign and prioritize QM resources based on risk and impact

  • Ensure timely and effective corrective and preventive actions

Quality risk identification, trending, and continuous improvement

  • Conduct trend analysis of GCO quality issues and audit findings

  • Identify systemic quality risks and emerging risk areas

  • Recommend and support process and system improvements

Audit and inspection readiness and support

  • Support audit and inspection preparation and execution

  • Ensure timely, high-quality responses and actions

  • Oversee implementation and effectiveness of audit actions

Ad hoc quality assessments and consultancy

  • Conduct ad hoc quality assessments

  • Recommend and oversee corrective actions

  • Provide quality consultancy to GCO leadership and teams

Oversight of site assessments

  • Oversee planning, conduct, and reporting of site assessments

  • Ensure appropriate follow-up actions are implemented

Global Support Center (GSC) oversight

  • Work closely with Global Support Centers, particularly APAC

  • Ensure quality delivery meets GCO standards

Compliance and professional standards

  • Exemplify compliance with Parexel standards, SOPs, and ICH GCP

  • Ensure accurate time recording and training completion

Additional responsibilities

  • Perform other quality-related responsibilities consistent with a Director-level role

Skills:

  • Excellent communication skills, including executive-level verbal and written communication, active listening, providing constructive feedback and facilitating group discussions.

  • Expert ability to think globally, strategically and analytically to problem-solve, make decisions keeping the patient and customer in focus. 

  • Excellent interpersonal skills, able to develop relationships and partnerships, build rapport, persuade and influence operational leaders, motivate others, manage performance and develop talent.

  • Effective change leader, able to understand and implement change while anticipating and managing resistance.

  • Expert manager with strong organizational and planning skills, competency in risk management with thoughtful action planning.

  • Personal awareness and emotionally intelligent, ability to self-motivate, innovate, delegate, and manage time as well as taking ownership and accountability for deliverables.

  • Ability to travel 10%-15%

Knowledge and Experience:

  • 15+ years’ experience in late phase clinical research

  • 7-10 years’ experience managing people

  • Expertise in ICH-GxPs

  • English proficiency (written and oral)

Education:

  • Bachelor’s Degree or other relevant experience required. Life science or other health-related discipline preferred.

  • Master’s Degree in a science, technology or industry-related discipline preferred.

Parexel Compensation & Benefits Highlights

The following summarizes recurring compensation and benefits themes identified from responses generated by popular LLMs to common candidate questions about Parexel and has not been reviewed or approved by Parexel.

  • Healthcare Strength Health coverage is described as comprehensive, including medical, dental, vision, HSA/FSA options, and company-paid disability insurance. Descriptions often portray the package as strong or “top notch,” adding meaningful value.
  • Retirement Support Retirement offerings include a 401(k) with company matching and, in some regions, generous pension contributions. Core financial protections are emphasized as a solid part of the total rewards.
  • Leave & Time Off Breadth Time-off programs include ample PTO or flexible/unlimited RTO alongside flexible schedules and remote/hybrid options. Work-life balance support from managers is highlighted as a practical advantage.

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The Company
HQ: Durham, North Carolina
20,524 Employees

What We Do

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.

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