Senior Clinical Research
6 days ago
Job Summary Our clinical operations activities are growing rapidly and we are currently seeking a full-time office-based Clinical Research CRA Manager to join our Clinical Monitoring team in Navi Mumbai India This position plays a key role in the clinical trial management process at Medpace If you want an exciting career where you use your previous expertise and can develop and grow your career even further then this is the opportunity for you Responsibilities Line management of Clinical Research Associates CRAs Recruitment initial and continued training and development of CRAs Oversight and Management of CRAs to ensure CRAs are meeting expectations of core monitoring responsibilities Tracking and management of CRA resourcing allocation of assignment and Manage turnover and retention of CRAs to meet company objectives Qualifications Bachelor s degree with 4-6 years pharmaceutical industry experience clinical monitoring or study management including 3 years as a CRA and 1-2 years as a CRA Manager preferred Advanced knowledge of Good Clinical Practice Strong leadership mentoring and motivational skills Effective written and verbal communication skills Proficient knowledge of Microsoft Office software and Occasional travel for evaluation of CRAs approximately 10 Medpace Overview 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 We leverage local regulatory and therapeutic expertise across all major areas including oncology cardiology metabolic disease endocrinology central nervous system anti-viral and anti-infective Headquartered in Cincinnati Ohio employing more than 5 000 people across 40 countries Why Medpace 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 who face hundreds of diseases across all key therapeutic areas The work we do today will improve the lives of people living with illness and disease in the future Medpace Perks Flexible work environment Competitive compensation and benefits package Competitive PTO packages Structured career paths with opportunities for professional growth Company-sponsored employee appreciation events Employee health and wellness initiatives Awards Recognized by Forbes as one of America s Most Successful Midsize Companies in 2021 2022 2023 and 2024 Continually recognized with CRO Leadership Awards from Life Science Leader magazine based on expertise quality capabilities reliability and compatibility What to Expect Next A Medpace team member will review your qualifications and if interested you will be contacted with details for next steps
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Mumbai, India Maxis Clinical Sciences Full timeJob Title: Clinical Quality Assurance Compliance & training Experience: 5 plus years Location: Mumbai Type: Full-time Experience Level: [Senior] Manager/Senior Manager Department: Clinical Research Department Purpose of this Role: This role will be responsible for oversight on end-to-end clinical trial activities from quality perspective. This role...
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Clinical Quality Assurance Compliance
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Mumbai, India Maxis Clinical Sciences Full timeJob Title: Clinical Quality Assurance Compliance & training Experience : 5 plus years Location: Mumbai Type: Full-time Experience Level: (Senior) Manager/Senior Manager Department: Clinical Research Department Purpose of this Role: This role will be responsible for oversight on end-to-end clinical trial activities from quality perspective. This role will be...
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Clinical Quality Assurance Compliance
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Mumbai, India Maxis Clinical Sciences Full timeJob Title: Clinical Quality Assurance Compliance & trainingExperience: 5 plus yearsLocation: MumbaiType: Full-timeExperience Level: [Senior] Manager/Senior ManagerDepartment: Clinical Research Department Purpose of this Role:This role will be responsible for oversight on end-to-end clinical trial activities from quality perspective. This role will be...
