Syneos Health Hiring Senior Clinical Research Associate

Syneos Health Hiring Senior Clinical Research Associate – Apply Now!

CRA II/Sr CRA II (Mumbai Location)

Location: IND-Client
Job ID: 25100047

About Syneos Health

Syneos Health is a globally recognized biopharmaceutical solutions organization dedicated to accelerating the delivery of innovative therapies to patients worldwide. With over 29,000 employees across 110 countries, Syneos Health provides comprehensive clinical development services, ensuring high-quality research and streamlined operations.

If you’re passionate about clinical research and looking for a rewarding career, Syneos Health is the place for you!

Job Overview – Senior Clinical Research Associate (CRA II / Sr CRA)

Current Openings:

• Position: CRA II / Sr CRA
• Location: Mumbai, Delhi, Bangalore, Hyderabad (Client-Based)
• Experience Required: Minimum 4 years in clinical research, with oncology and cardiovascular therapeutic area experience preferred
• Qualification: Bachelor’s degree or RN in a relevant field
• Travel: Up to 75% (as required)

Key Responsibilities

• Looking for min 4 years of onsite monitoring experience
• good experience in oncology therapeutic area
• client based opportunity, candidate from Mumbai location preferred.
• Conduct on-site and remote monitoring of clinical research studies to ensure compliance with widely accepted clinical practices, including reviewing study protocols, informed consent forms, and case report forms
• Develop and implement tools, procedures, and processes to ensure quality monitoring, such as creating monitoring plans, checklists, and templates
• Contribute to the design, implementation, and delivery of processes, programs, and policies, including participating in the development of standard operating procedures (SOPs) and training materials
• Manage defined components of projects or processes within the area of responsibility, such as coordinating site visits, tracking study progress, and resolving issues
• Ensure accurate and timely documentation of monitoring activities and findings, including writing monitoring reports, follow-up letters, and action plans
• Collaborate with cross-functional teams to support clinical trial operations, including working with investigators, site staff, and other stakeholders to ensure smooth study conduct

Required Qualifications

• • Bachelor’s degree in a related field or equivalent experience
  • Minimum of 2-4 years of experience in clinical research monitoring
  • Strong knowledge of Good Clinical Practice (GCP) guidelines and regulatory requirements
  • Excellent communication and interpersonal skills
  • Ability to work independently and manage multiple priorities
  • Proficiency in using clinical trial management systems and other relevant software

  Certifications:

  • Certified Clinical Research Associate (CCRA) or equivalent certification preferred

  Necessary Skills:

  • Attention to detail and strong analytical skills
  • Problem-solving abilities and critical thinking
  • Ability to work effectively in a team environment
  • Strong organizational and time management skills
  • Proficiency in Microsoft Office Suite

How to Apply

If you meet the qualifications and are ready to advance your career in clinical research, apply now! Lick the  link below to submit your application:

Apply Now