Welcome Back

Google icon Sign in with Google
OR
I agree to abide by Pharmadaily Terms of Service and its Privacy Policy

Create Account

Google icon Sign up with Google
OR
By signing up, you agree to our Terms of Service and Privacy Policy
Instagram
youtube
Facebook

Clinical Operations Manager

Parexel
Parexel
7-10 years
Not Disclosed
Bangalore, India
10 Feb. 16, 2026
Job Description
Job Type: Full Time Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Clinical Operations Manager – Bengaluru, India

Location: Bengaluru, Karnataka, India
Job Category: Clinical Trials / Clinical Operations
Experience Required: 7–10 years in clinical research or clinical operations management


About Parexel

Parexel is a global leader in clinical research and biopharmaceutical services, providing innovative solutions across clinical trials, regulatory affairs, and patient-centric healthcare. Our teams deliver high-quality results while maintaining compliance with international standards, supporting life-changing therapies worldwide. At Parexel, you will be part of a collaborative and inclusive culture that prioritizes professional growth, scientific excellence, and operational efficiency.


Role Overview

The Clinical Operations Manager oversees clinical project teams to ensure timely delivery, high-quality performance, and operational excellence. This role involves team management, project oversight, client liaison, and contribution to business development initiatives. The Manager works independently under the guidance of Senior Managers, Associate Directors, or Directors, and may also participate as a project contributor.


Key Responsibilities

Project Delivery & Oversight

  • Monitor project performance and ensure deliverables meet timelines, quality standards, and sponsor expectations.

  • Serve as a senior contributor on projects, including preparation of status reports, documentation reviews, and attending project team meetings.

  • Facilitate metrics collection, develop action plans, and support project leadership to keep studies on time and within budget.

  • Manage resource allocation, staff assignments, and ensure the efficiency and quality of project deliverables.

  • Act as liaison between project teams, sponsors, and management regarding team performance and project progress.

Team & Talent Management

  • Mentor and guide staff to ensure they have the technical knowledge and resources to meet project goals.

  • Conduct quality checks of deliverables, provide feedback, and implement corrective actions as needed.

  • Support career development, performance management, and skill enhancement of team members.

  • Allocate staff effectively according to expertise and project requirements, ensuring high team engagement and retention.

Client Management & Business Development

  • Participate in client interactions, project bids, and presentations as appropriate.

  • Coordinate client or account activities, addressing feedback and ensuring client satisfaction.

  • Promote Parexel’s services and capabilities to support business growth and retention.

Operational Excellence & Compliance

  • Maintain compliance with ICH Guidelines, Good Clinical Practices (GCP), regulatory requirements, and Parexel SOPs.

  • Implement departmental and system improvement initiatives to enhance operational efficiency.

  • Maintain productivity, monitor staff turnover, and manage routine administrative tasks including timesheets, travel, and training documentation.

  • Foster a positive, results-oriented environment, promoting teamwork, transparency, and effective communication.

Leadership & Role Modeling

  • Act as a role model for clinical operations teams, demonstrating leadership, accountability, and adherence to corporate policies.

  • Participate in location or functional management meetings and initiatives, contributing to organizational growth.


Required Skills & Competencies

  • Proven ability to manage and motivate teams in a clinical research environment.

  • Strong leadership, problem-solving, and decision-making capabilities.

  • Excellent oral and written communication skills in English; local language proficiency preferred.

  • Strong understanding of clinical trial operations, study monitoring, and data management.

  • Ability to manage multiple projects simultaneously while meeting deadlines.

  • Proficient in project management tools and Microsoft Office applications.


Education & Experience

  • Bachelor’s or Master’s degree in Biological Sciences, Pharmacy, Nursing, or other health-related discipline.

  • Experience: 7–10 years in clinical research, clinical operations, or equivalent roles with substantial project management experience.

  • Prior experience in team leadership, resource management, and client-facing roles is preferred.


Why Join Parexel

  • Lead high-impact clinical trials for global pharmaceutical clients.

  • Work in a collaborative, inclusive, and professional environment.

  • Access professional development opportunities, mentorship, and career growth pathways.

  • Contribute to the development of life-changing therapies that improve patient outcomes worldwide.