Are you passionate about advancing clinical research and ensuring patient safety? Pfizer, a global leader in pharmaceuticals, is hiring a Site Care Partner in Mumbai, India, to support clinical trial operations. This full-time role offers an opportunity to collaborate with investigative sites, drive study success, and contribute to groundbreaking medical advancements. If you have experience in site management and a knack for building relationships, this is your chance to join a dynamic team at Pfizer.
Key Responsibilities
As a Site Care Partner, you will play a pivotal role in managing clinical trial sites, ensuring quality, compliance, and timely execution. Your responsibilities will include:
- Site Start-Up and Activation: Oversee site qualification, activation, and study start-up activities, including protocol feasibility assessments and site initiation visits (SIVs).
- Relationship Building: Establish and maintain strong relationships with investigator sites and strategic partners to ensure smooth study operations.
- Recruitment and Enrollment: Develop and execute site-level recruitment strategies to meet global and local enrollment targets.
- Quality and Compliance: Utilize analytic tools (e.g., SQRD, IRMS) to monitor site quality, identify risks, and implement mitigation plans.
- Collaboration: Work closely with Clinical Research Associates (CRAs), Site Activation Partners, and other stakeholders to optimize site performance.
- Local Intelligence: Provide country-specific insights to support site selection, protocol feasibility, and regulatory compliance.
- Study Conduct and Close-Out: Ensure quality monitoring, resolve escalated site issues, and support study close-out activities.
- Scientific Communication: Write scientific summaries for Subject Expert Committees and coordinate with local medical, regulatory, and commercial teams.
Qualifications and Skills
To excel in this role, candidates should meet the following requirements:
- Education: Graduate or Post-Graduate degree in Pharmacy, Biotechnology, Nursing, MBBS/MD, or a related field.
- Experience: 8–12 years of experience in clinical research, including site management, site monitoring (CRA experience), and start-up/close-out activities.
- Technical Skills: Knowledge of Good Clinical Practice (GCP), ICH Guidelines, and regulatory requirements. Proficiency in computer systems and adaptability to new technologies.
- Communication: Strong verbal and written communication skills in English; proficiency in local languages is a plus.
- Interpersonal Skills: Ability to build cross-functional relationships, manage stakeholder interactions, and adapt to changing processes.
- Travel: Willingness to travel nationally and internationally as needed.
Benefits of Working at Pfizer
Joining Pfizer as a Site Care Partner offers numerous benefits:
- Career Growth: Work with a global leader in pharmaceuticals and gain exposure to cutting-edge clinical research.
- Impactful Work: Contribute to patient safety and the development of life-changing therapies.
- Collaborative Environment: Partner with diverse teams across clinical operations, regulatory affairs, and medical teams.
- Equal Opportunity Employer: Pfizer fosters an inclusive workplace that values diversity and complies with equal employment opportunity laws.
