Site Care Partner - Mumbai

Planet Pharma; Mumbai; On-site; INR 1,500,000 - 2,100,000; Full time

Job summary

Planet Pharma is seeking a Site Care Partner in Mumbai to lead relationships with clinical trial sites and drive engagement across protocols and regulatory requirements.

Role focuses on onsite site operations, collaboration with cross-functional teams, and delivering proactive engagement strategies to optimize trial performance. Travel up to 60% is expected.

Qualifications

• 8+ years of onsite monitoring experience in a multinational company.
• 5+ years in project or clinical trial management.
• Proven ability to manage entire site operations independently.
• Experience with SEC presentations to Regulatory Authorities is a plus.
• Strong interpersonal, communication, and organizational skills.

Responsibilities

• Build and nurture relationships with principal investigators, site coordinators, and research staff at clinical trial sites.
• Support site staff with study protocols, regulatory compliance, and operational procedures.
• Identify opportunities to enhance site engagement and optimize performance through proactive communication.
• Collaborate with internal teams to develop tailored site engagement strategies.
• Monitor site performance metrics and provide insights on engagement activities and outcomes.

Skills

Onsite monitoring

Project management

Clinical trial management

ICH-GCP

Travel up to 60%

Education

Bachelor's/Master's in Life Sciences

Tools

Clinical trial tools

Job description

Exciting Opportunity: Site Care Partner - MumbaiAre you a seasoned clinical research professional craving a dynamic role that blends site management, stakeholder engagement, and impactful collaboration? Join our CRO client as a Site Care Partner in Mumbai and play a crucial part in advancing innovative therapies for global patients. This strategic position offers the chance to work directly onsite with an innovative pharma, fostering strong relationships with clinical trial sites while contributing to cutting-edge medical advancements. If you're ready to make a meaningful difference and thrive in a fast-paced environment, this is your moment!

What You Will Do

• Build and nurture relationships with principal investigators, site coordinators, and research staff at clinical trial sites.
• Support site staff with study protocols, regulatory compliance, and operational procedures.
• Identify opportunities to enhance site engagement and optimize performance through proactive communication.
• Collaborate with internal teams to develop tailored site engagement strategies.
• Monitor site performance metrics and provide insights on engagement activities and outcomes.

Required Skills & Qualifications

• Bachelor's or Master's degree in life sciences or a related field.
• Minimum of 8+ years of onsite monitoring experience in a multinational company, with at least 5 years in project or clinical trial management.
• Proven ability to manage entire site operations independently.
• Experience with Subject Expert Committee (SEC) presentations to Regulatory Authorities is a plus.
• Strong interpersonal, communication, and organizational skills.
• In-depth knowledge of ICH-GCP guidelines and clinical trial regulatory requirements.
• Willingness to travel up to 60% as required.

Nice To Have Skills

• Expertise in project oversight and strategic site engagement initiatives.
• Familiarity with SIVs (Site Initiation Visits) and clinical trial project management tools.

Preferred Education & Experience

• Relevant bachelor’s or master’s degree in life sciences or a related field.
• Extensive onsite monitoring experience within an MNC environment.
• Prior experience working with regulatory authorities and conducting SEC presentations.