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 deep therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, Medpace employs approximately 2,500 people across 35 countries
Post : Clinical Research Associate
Responsibilities
1.Conduct pre-study, initiation, monitoring, and closeout visits for research sites according to Medpace/Sponsor SOPs and GCP;
2. Maintain ongoing site correspondence and site files;
3.Complete visit reports and maintaining study-related databases;
4.Oversight and interaction with clinical research sites; and
5. Review of patient charts and clinical research data.
1.Conduct pre-study, initiation, monitoring, and closeout visits for research sites according to Medpace/Sponsor SOPs and GCP;
2. Maintain ongoing site correspondence and site files;
3.Complete visit reports and maintaining study-related databases;
4.Oversight and interaction with clinical research sites; and
5. Review of patient charts and clinical research data.
Candidate Profile
* University degree in health-related field;
* 2- 4 years of monitoring experience gained from a global CRO and /or other related clinical research environment is preferred;
* Proven track record of demonstrating experience in clinical patient management, protocol, CRF, preparing of ISF, documentation to be submitted to competent authorities, project management;
* Computer literacy;
* Excellent verbal and written communication skills in English.
* Should be both a team worker and self-motivated professional ;
* Detailed-minded & well-organized;
* Strong determination to grow with the organization.
* University degree in health-related field;
* 2- 4 years of monitoring experience gained from a global CRO and /or other related clinical research environment is preferred;
* Proven track record of demonstrating experience in clinical patient management, protocol, CRF, preparing of ISF, documentation to be submitted to competent authorities, project management;
* Computer literacy;
* Excellent verbal and written communication skills in English.
* Should be both a team worker and self-motivated professional ;
* Detailed-minded & well-organized;
* Strong determination to grow with the organization.
Additional Information:
Qualification: University degree in health-related
Location: Navi Mumbai
Industry Type: Pharma/ Biotech/Clinical Research
Functional Area: CRA
End Date: 20th June, 2017
Qualification: University degree in health-related
Location: Navi Mumbai
Industry Type: Pharma/ Biotech/Clinical Research
Functional Area: CRA
End Date: 20th June, 2017
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