Clinical Project Manager

Clario; Bengaluru; Remote; INR 1,200,000 - 1,800,000; Full time

Benefits offered by this job

Provident fund

Medical insurance

Employee programs & events

Remote work flexibility

Job summary

Clario is seeking a Clinical Project Manager to lead imaging-enabled clinical trials in India. You will drive study start-up, execution, and closeout while coordinating sponsors, sites, and cross-functional teams to maintain timelines, quality, and budget adherence.

Ideal candidates have 1–3 years in CRO/pharma trials, knowledge of GCP/ICH, and comfort with MS Office and project tools. Remote work flexibility is offered with local office options.

Qualifications

• Bachelor’s degree or equivalent in life sciences or healthcare.
• 1–3 years in clinical trials within CRO or pharma settings.
• Experience with clinical development of investigational medicines.
• Familiarity with GCP, ICH, and clinical regulations.
• Medical imaging experience is a plus.

Responsibilities

• Lead study start-up activities and translate requirements into plans and docs.
• Manage project execution and sponsor communications with stakeholders.
• Monitor risks, data collection, and delivery against plans.
• Own financials: billing, forecasting, amendments, costs.
• Coordinate study closeout and submission activities.

Skills

GCP knowledge

ICH guidelines

Project management

Clinical trials

Medical imaging

Education

Bachelor's in life sciences

Tools

MS Word

MS Excel

MS Project

Job description

## Clinical Project ManagerApply: India Remote: Bangalore, India: Full time: Posted Today: R18443Join Clario, a part of Thermo Fisher Scientific, as a Clinical Project Manager supporting medical imaging programs in India. You will lead the delivery of clinical trial projects from study start-up through closeout, connecting sponsors, sites and cross-functional teams while maintaining quality, timelines, financial oversight and protocol compliance. This is an opportunity to combine clinical project leadership with work that helps bring life-changing therapies to patients faster. ## What We Offer * Competitive compensation and incentives* Provident fund and medical insurance* Engaging employee programs and local events* Modern office spaces and remote work flexibility ## What You’ll Be Doing * Lead clinical study start-up activities, translating study requirements and response assessment criteria into project plans, timelines, milestones, communication plans and study documentation.* Manage project execution and stakeholder communications, providing timely updates to sponsor representatives, project teams, sites, Business Development and leadership.* Monitor critical project success factors, resource requirements, risks, data collection activities and overall delivery against agreed project expectations.* Own key financial activities, including monthly billing, forecasting, scope reviews, amendments, pass-through costs and the project information required to support revenue reporting.* Maintain strong knowledge of project contracts, study protocols and Standard Operating Procedures (SOPs), partnering with Quality Assurance to address deviations and communicate protocol updates.* Lead, train and support cross-functional project teams, establishing clear project expectations and partnering with functional leaders on coaching and development.* Support Business Development activities through capabilities discussions, sponsor meetings and polished Investigator Meeting presentations.* Coordinate study closeout and applicable submission activities, ensuring project deliverables are completed appropriately.* Where applicable, provide people-management support, including setting expectations, coaching, performance management, hiring and onboarding. ## What We Look For * Bachelor’s degree or equivalent practical experience; education in life sciences, pharmacy, nursing or another healthcare field is highly desirable.* 1–3 years of clinical trials experience within a contract research organization (CRO) or pharmaceutical research environment, preferably in project management.* Previous project or management experience supporting the clinical development of investigational medicines.* Working knowledge of Good Clinical Practice (GCP), International Council for Harmonisation (ICH) guidelines and relevant clinical research regulations.* Medical imaging experience is preferred.* Experience with common project and business productivity tools, including Microsoft Word and Excel; Microsoft Project experience is preferred.* Demonstrated ability to organize and lead complex clinical projects while managing timelines, financial activities and multiple stakeholders.* Strong written and verbal communication skills with a collaborative, professional approach.* Ability to work effectively with sponsors, investigative sites and cross-functional teams in a quality-focused clinical research environment. At Clario, a part of Thermo Fisher Scientific, a part of Thermo Fisher Scientific, our purpose is to transform lives by unlocking better evidence. It’s a cause that unites and inspires us. It’s why we come to work—and how we empower our people to make a positive impact every day. Whether you're advancing clinical science, building innovative technology, or supporting our global teams, your work helps bring life-changing therapies to patients faster.