SITE CARE PARTNER MUMBAI

Planet Pharma; Mumbai; On-site; INR 1,400,000 - 1,800,000; Full time

Job summary

Planet Pharma in Mumbai is seeking an experienced Site Care Partner to manage clinical trial sites onsite and engage stakeholders across sponsors, sites, and regulatory bodies. You will drive protocol adherence, regulatory compliance, and operational excellence at multiple sites in India.

The ideal candidate has 8+ years of onsite monitoring, 5+ years in project or trial management, strong ICH-GCP knowledge, and willingness to travel up to 60% while collaborating with global teams.

Qualifications

• Bachelor’s or Master’s degree in life sciences or related field.
• 8+ years of onsite monitoring in a multinational company, with at least 5 years in project or clinical trial management.
• Ability to manage entire site operations independently.
• Willingness to travel up to 60% as required.

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 trials

ICH-GCP knowledge

Regulatory compliance

Stakeholder engagement

Education

Bachelor or Master in life sciences

Job description

Job Description:

Site Care Partner – Mumbai

Location: Onsite - Mumbai, Maharashtra

Category: Clinical Development and Operations

Salary: Apply for details

Country: India

Employment: Direct Hire/Perm

Worksite: On-Site

Exciting Opportunity: Site Care Partner – Mumbai

Are 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.

If you’re ready to bring your expertise to a globally recognized company and make a difference in clinical research,

Equal Opportunity Employer

We are proud to be an equal opportunity employer. We welcome and encourage applications from all qualified candidates regardless of race, sex, gender identity or expression, disability, age, religion or belief, sexual orientation, or any other characteristic protected by applicable laws and regulations. It is our policy not to discriminate against any applicant or employee, and we are committed to fostering a diverse, inclusive, and respectful work environment across all locations in which we operate. We believe that diversity, equity, and inclusion are fundamental to our mission and enhance our ability to serve clients globally. If you have a disability or require any reasonable accommodations during the application or interview process, please inform your recruiter or contact us(opens in new tab) directly so that we can explore the appropriate arrangements.