Project Specialist (clinical experience)

Jobgether; India; On-site; INR 900,000 - 1,300,000; Full time

Job summary

Jobgether on behalf of a partner company in India seeks a Project Specialist (Clinical Experience) to coordinate clinical study activities and manage timelines. The role involves collaboration with clinical operations, regulatory affairs, and data management to ensure milestones are met and regulatory compliance is maintained.

The ideal candidate will support budget management, process standardization, and patient recruitment strategies in a dynamic clinical research environment aimed at

Qualifications

• General understanding of clinical project management principles.
• Experience in coordinating cross-functional teams.

Responsibilities

• Develop, coordinate, and communicate clinical study timelines and milestones.
• Coordinate input from clinical, regulatory, data management and other teams.
• Oversee study operations and ensure SOPs, GCP and country regulations compliance.
• Promote standardized procedures and continuous operational improvement.
• Assist in site and vendor selection and contract negotiations.
• Monitor budgets, expenditures, and financial reporting for studies.
• Track study progress and address deviations with corrective actions.
• Support development and implementation of clinical development strategies.
• Coordinate patient recruitment and enrollment activities.
• Maintain accurate project records and communicate risks and updates.

Skills

Excel

MS Word

PowerPoint

Project management

Communication

Analytical thinking

Adaptability

Ownership

Education

High school diploma or equivalent

Associate degree or higher preferred

Tools

Microsoft Office

Job description

This position is listed on behalf of a partner company, who manages all applications and next steps. Our partner is looking for a Project Specialist (Clinical Experience) based in India.

Join a collaborative clinical research environment dedicated to advancing healthcare and accelerating the development of innovative treatments. In this role, you will coordinate clinical study activities, manage timelines, and support the successful delivery of clinical trials. You will work closely with cross-functional teams, including clinical operations, regulatory affairs, and data management, to ensure project milestones are achieved efficiently. Your expertise will contribute to maintaining regulatory compliance, optimizing study budgets, and resolving operational challenges. You will also help standardize processes, monitor study performance, and develop effective patient recruitment strategies. This opportunity is ideal for an organized, detail-oriented professional who thrives in a dynamic environment and wants to make a meaningful contribution to clinical research and patient outcomes.

Accountabilities

• Clinical Project Planning: Develop, coordinate, and communicate clinical study timelines, ensuring key milestones and deliverables are achieved according to project objectives.
• Cross-Functional Coordination: Gather input from clinical, regulatory, data management, and other relevant teams to develop comprehensive project plans and facilitate timely execution.
• Study Operations and Compliance: Oversee clinical trial activities, resolve operational challenges, and ensure compliance with standard operating procedures (SOPs), Good Clinical Practice (GCP), and applicable country-specific regulations.
• Process Improvement: Promote consistency across clinical studies by standardizing procedures, implementing best practices, and supporting continuous operational improvement.
• Site and Vendor Management: Support the selection of clinical research sites and vendors, participate in contract negotiations, and maintain productive relationships to ensure quality and timely service delivery.
• Budget Management and Financial Reporting: Prepare and monitor clinical study budgets, review expenditures, perform financial analysis, and help ensure projects remain within approved financial parameters.
• Performance Monitoring: Track study progress, monitor key performance indicators, identify deviations from established plans, and follow up with project team members and line managers to implement corrective actions.
• Clinical Development Strategy: Support the development and implementation of clinical development strategies, ensuring alignment between study activities and overall project goals.
• Patient Recruitment and Enrollment: Develop and coordinate recruitment strategies, identify target populations, support the creation of recruitment materials, and monitor enrollment progress against study targets.
• Reporting and Documentation: Maintain accurate project records, prepare status reports, and communicate risks, progress, and operational updates to relevant stakeholders.

Requirements

• Education: High school diploma or equivalent required; an associate degree or higher in a relevant field is preferred. Equivalent combinations of education and experience may be considered.
• Clinical Experience: At least one year of relevant experience is indicated in the initial role requirements, while the detailed qualifications specify a minimum of three years in clinical project management or a related field.
• Clinical Research Knowledge: A solid understanding of clinical trial processes, study coordination, regulatory requirements, and clinical project management principles.
• Regulatory Compliance: Familiarity with SOPs, ICH-GCP guidelines, and country-specific clinical research regulations.
• Technical Skills: Advanced Microsoft Excel proficiency for financial reviews, data analysis, and reporting, along with working knowledge of Microsoft Word, PowerPoint, and other Microsoft Office applications.
• Project Management Skills: Strong organizational, planning, multitasking, and time management abilities, with the capacity to manage competing priorities and meet demanding deadlines.
• Communication and Collaboration: Excellent written and verbal communication skills, effective interpersonal abilities, and the confidence to coordinate with cross-functional teams and external stakeholders.
• Analytical Thinking: Strong attention to detail, problem-solving capabilities, and the ability to identify operational risks, investigate discrepancies, and recommend practical solutions.
• Adaptability and Ownership: Ability to work independently and collaboratively, respond effectively to changing priorities, and remain productive under pressure.
• Preferred Certifications: Certification in clinical project management or a related discipline is an advantage. Good Clinical Practice (GCP) certification is also preferred.

Benefits

• Opportunities for professional development, career progression, and long-term growth within the clinical research industry.
• Supportive management and access to technical, therapeutic-area, and role-specific training.
• Peer recognition initiatives and a total rewards program.
• An inclusive and collaborative work environment that values diverse perspectives, teamwork, and continuous learning.
• Opportunities to collaborate with multidisciplinary and international teams on clinical research projects.
• The opportunity to contribute to the development of innovative treatments and healthcare solutions that can improve patient outcomes.
• Exposure to clinical studies across different therapeutic areas and stages of development.
• Compensation, healthcare coverage, leave entitlements, and work arrangements: Specific details were not provided in the original job description and should be confirmed during the recruitment process.