Medpace, a global leader in clinical contract research, is seeking dedicated individuals to join their team as Clinical Research Associates (CRA) at the entry level in Navi Mumbai, India. This role offers an exciting opportunity to contribute to the development of life-saving pharmaceuticals and medical devices, with comprehensive training and growth potential in a dynamic work environment.
Company Overview: Medpace
Medpace is a full-service clinical contract research organization (CRO) that provides Phase I-IV clinical development services to biotechnology, pharmaceutical, and medical device industries. With a mission to accelerate the global development of safe and effective medical therapeutics, Medpace employs a disciplined approach, leveraging regulatory and therapeutic expertise across all major areas, including oncology, cardiology, and central nervous systems. Headquartered in Cincinnati, Ohio, Medpace operates in nearly 40 countries, employing over 4,000 people globally.
Key Responsibilities of a Clinical Research Associate (CRA) Entry
As an entry-level CRA at Medpace, you will be responsible for a range of essential tasks, including:
- Site Visits: Conducting qualification, initiation, monitoring, and closeout visits for research sites in compliance with approved protocols.
- Communication: Maintaining communication with medical site staff, including coordinators, clinical research physicians, and site personnel.
- Documentation Verification: Verifying medical records and research source documentation against case report form data, ensuring accuracy and adherence to good documentation practices.
- Eligibility Verification: Ensuring that investigators enroll only eligible subjects by reviewing qualifications, training, and available resources.
- Regulatory Compliance: Reviewing regulatory documents and verifying the accountability and inventory of medical devices and investigational products.
- Adverse Event Reporting: Reviewing adverse events, serious adverse events, concomitant medications, and corresponding illnesses to confirm accurate data reporting.
- Recruitment and Retention: Assessing patient recruitment and retention success at clinical research sites and offering improvement suggestions.
- Reporting: Completing monitoring reports and follow-up letters, summarizing significant findings, deviations, deficiencies, and recommended actions to secure compliance.
Qualifications and Skills Required
Candidates interested in the CRA Entry position at Medpace should meet the following qualifications:
- Educational Background: A minimum of a bachelor’s degree, preferably in a health or life science-related field.
- Experience: Experience as a Clinical Research Coordinator is advantageous, but not required.
- Travel: Willingness to travel approximately 60-80% nationally.
- Technical Skills: Familiarity with Microsoft® Office applications.
- Communication: Strong communication and presentation skills are highly valued.
Training and Development: PACE® – Medpace CRA Training Program
Medpace offers comprehensive initial and ongoing training through its PACE® Training Program, designed to develop your skills as a Clinical Research Associate. This program provides:
- Hands-on Training: Interactive discussions, job-related exercises, and practicums to build your CRA capabilities.
- Core Rotations: Participation in clinical research departmental rotations to learn various aspects of the drug/device development and approval process.
- Professional Growth: A defined CRA promotion and growth ladder with potential for mentoring and management advancements.
How to Apply for the Clinical Research Associate (CRA) Entry Position
If you are ready to embark on a rewarding career as a Clinical Research Associate with Medpace, apply now through the Medpace Careers page. Search for the job requisition number 10129 to begin your application process. Highlight your relevant experience, educational background, and eagerness to contribute to the development of medical therapeutics.
