Job Title: eClinical Coordinator
Location: Navi Mumbai, India
Summary:
Medpace, a leading global Clinical Research Organization (CRO), is seeking a highly motivated and detail-oriented eClinical Coordinator to join our growing team in Navi Mumbai, India. This full-time position offers an excellent opportunity to contribute to the success of global clinical trials by ensuring the accuracy and integrity of clinical data. As an eClinical Coordinator, you will play a vital role in supporting data management activities, system setup, and compliance within our dynamic and collaborative environment. If you are passionate about clinical research, possess strong organizational skills, and are looking to advance your career with a recognized industry leader, we encourage you to apply.
About Medpace:
Medpace is a scientifically-driven, global full-service clinical contract research organization (CRO) providing Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Medpace’s mission is to accelerate the global development of safe and effective medical therapeutics through its high-science and disciplined operating approach. We leverage local regulatory and therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral and anti-infectious.
Key Responsibilities:
As an eClinical Coordinator, you will be an integral part of the clinical data management team, responsible for supporting the successful execution of clinical trials. Your primary responsibilities will include:
- System Design and Setup: Assisting Project Managers in the design and implementation of eClinical systems, ensuring they meet study-specific requirements and regulatory guidelines.
- Documentation Management: Creating and maintaining study-specific documentation, including user manuals, training materials, and standard operating procedures (SOPs).
- Data Tracking and Reporting: Tracking key study metrics and progress, generating reports, and identifying potential issues or delays.
- Client Collaboration: Collaborating with clients to gather requirements, address queries, and provide ongoing support.
- Data Management Tasks: Performing various data management and eClinical tasks, such as data validation, data cleaning, and data reconciliation.
- Quality Assurance: Ensuring the quality and integrity of clinical data through rigorous review and adherence to established quality control procedures.
- Compliance: Maintaining compliance with all applicable regulations and guidelines, including Good Clinical Practice (GCP) and data privacy regulations.
Qualifications & Requirements:
To be successful in this role, candidates should possess the following qualifications and experience:
- Educational Background: A Bachelor’s degree in a health-related field such as Pharmacy, Life Sciences, or Biotechnology is required.
- Technical Skills: Demonstrated proficiency in Microsoft Excel and Word, with strong attention to detail and accuracy.
- Medical Knowledge: A working knowledge of medical terminology is essential.
- Relevant Experience: 1-2 years of experience in a pharmaceutical or CRO setting is preferred, particularly in data management or eClinical roles.
- Communication Skills: Excellent written and verbal communication skills, with the ability to effectively communicate with internal teams and external clients.
- Organizational Skills: Strong organizational and time-management skills, with the ability to manage multiple tasks and prioritize effectively.
- Work Environment: No travel is required for this position.
Why Join Medpace?
Medpace offers a rewarding and challenging work environment where employees are valued and recognized for their contributions. We are committed to providing our employees with opportunities for professional growth and development, as well as a comprehensive benefits package that includes:
- Flexible Work Environment: Hybrid work options are available to promote work-life balance.
- Competitive Compensation: A competitive salary and benefits package are offered, commensurate with experience and qualifications.
- Generous Paid Time Off: A generous paid time off (PTO) policy is provided to support employee well-being and work-life integration.
- Wellness Initiatives: Various wellness programs and initiatives are available to promote employee health and well-being.
- Career Growth: Structured career growth and professional development programs are in place to support employee advancement.
- Employee Recognition: Regular employee appreciation events and recognition programs are implemented to acknowledge employee achievements.
Medpace’s commitment to excellence has been recognized by Forbes as one of America’s Most Successful Midsize Companies (2021-2024). We also consistently earn CRO Leadership Awards for quality, reliability, and expertise, demonstrating our dedication to providing the highest quality services to our clients.
How to Apply:
If you are a highly motivated and qualified candidate seeking a challenging and rewarding career in clinical research, we encourage you to apply for the eClinical Coordinator position at Medpace. Please submit your resume and cover letter for consideration. We look forward to hearing from you!