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CRA job opportunities are highly sought after in the clinical research field, and this role at Medpace offers an excellent entry point into global clinical trials. If you have a background in life sciences and are looking for life science jobs in Spain, this Clinical Research Associate position in Barcelona could be your ideal career move.
- Job Position: Clinical Research Associate
- Location: Barcelona, Spain
- Job ID: 12065
About the Company
CRA job Medpace is a full-service clinical contract research organization (CRO). We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through its scientific and disciplined approach. Headquartered in Cincinnati, Ohio, employing more than 5,000 people across 40+ countries.
Job Description
CRA job Our CRA Team is currently seeking a full-time home-based CRA located in Barcelona and the surrounding areas.
For those with medical and/or health/life science interest and background who want to explore the research field and be part of a team bringing pharmaceutical and medical devices to market – this could be the right opportunity for you!
Our successful Clinical Research Associates possess varied backgrounds in medical and other science-related healthcare fields.
Qualifications
CRA job Must have:
- Minimum of a university degree in a life science related field
- Minimum 1 year of experience as a Study Coordinator (SC), Clinical Research Coordinator (CRC), or CRA trainee
- Approximately 60-80% travel availability
- Proficient knowledge of Microsoft® Office and general computer literacy
- Outstanding communication and presentation skills
- Strong attention to detail and time management
- Excellent verbal and written communication skills in English and Spanish
- Fluency in Catalan will be considered an asset
PACE – Medpace CRA Training Program
CRA job Medpace provides comprehensive initial and ongoing training, unmatched by other CROs.
Through our PACE Training Program, you will join other Professionals Achieving CRA Excellence:
- PACE provides the platform to effectively and confidently carry out your duties, enhance your current abilities and ultimately help you become a high-functioning independent Medpace CRA.
- PACE will prepare you by developing your CRA skills through interactive discussions and hands on job-related exercises and practicums.
- To supplement your in-house and field-based training you may also participate in other clinical research departmental core rotations, learning other aspects of the drug/device development and approval process.
Key Responsibilities
CRA job As a CRA, you will specifically be responsible for the following:
- Conduction of qualification, initiation, monitoring, and closeout visits for research sites in compliance with the approved protocol
- Communication with the medical site staff including coordinators, clinical research physicians and their site staff
- Verifying adequate investigator qualifications, training and resources
- Medical record and research source documentation verification against case report form data
- Ensuring good documentation practices and communicating protocol deviations appropriately
- Verification that the investigator is enrolling only eligible subjects
- Regulatory document review
- Medical device and/or investigational product/drug accountability and inventory
- Verification and review of adverse events and data reporting accuracy
- Assessing patient recruitment and retention success
- Completion of monitoring reports and follow-up letters
Why Medpace?
CRA job People. Purpose. Passion. Make a Difference Tomorrow. Join Us Today.
The work we’ve done over the past 30+ years has positively impacted the lives of countless patients and families across multiple therapeutic areas. The work we do today will improve the lives of people living with illness and disease in the future.
