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Clinical Trial Manager Posted by Medpace Clinical Research India Navi Mumbai Posted: imported by Jeevika JobsPopular categoriesIT jobsSales jobsMarketing jobsData Science jobsHR jobsEngineering jobsJobs in demandFresher jobsMNC jobsRemote jobsWork from home jobsWalk-in jobsPart-time jobsJobs by locationJobs in DelhiJobs in MumbaiJobs in BangaloreJobs in HyderabadJobs in ChennaiJobs in PuneCompaniesExplore categoriesUnicornMNCStartupProduct basedInternetExplore collectionsTop companiesIT companiesFintech companiesSponsored companiesFeatured companiesResearch companies by AmbitionboxInterview questionsCompany salariesCompany reviewsSalary CalculatorServicesAI career toolsNeo AI job agentResume score checkerAI resume makerInterview Q&AAI mock interviewLive AI interviewPremium servicesNaukri ProMost popularExpert resume writingExpert power profileAI BootcampsNewFree resourcesResume samplesJob letter samplesSearch jobs hereLoginRegisterFor employersBuy onlineNaukri Talent CloudEmployer LoginClinical Trial ManagerMedpace Clinical Research India4.213 Reviews0 - 2 yearsNot DisclosedNavi MumbaiPosted: 3+ weeks agoApplicants: 100+Clinical Trial ManagerMedpace Clinical Research India4.213 ReviewsJob description TitleMedpace is the leading CRO for Biotech companies and is continuing to add Clinical Trial Managers of different experience levels to join our Clinical Trial Management Group in Navi Mumbai, India Office. Clinical Trial Managers with expertise in Cardiovascular, Renal, Metabolic or Gastrointestinal related are welcome to continue to work in their area of expertise or to expand to a new therapeutic area. OverviewMedpace is a full-service clinical contract research organization (CRO) providing phase l-lV 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 the advancement of clinical research. We leverage in-country regulatory and therapeutic expertise across all major therapeutic areas including oncology, cardiology, metabolic, endocrinology, central nervous system, and anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, we employ more than 6,500 people across 40+ countries. Responsibilities Manage and provide accountability for day-to-day operations of the project, as defined by the contract and according to ICH/GCP and all other applicable laws, rules, and regulations; Serve as primary Sponsor contact for operational project-specific issues and study deliverables; Maintain in depth knowledge of protocol, therapeutic area, and indication; Provide cross-functional oversight of internal project team members and deliverables, which includes ensuring all necessary project-specific training is provided; Review and provide input for study protocol, edit check specifications, data analysis plan, and final study report, when applicable; Develop operational project plans; Manage risk assessment and execution; Responsible for management of study vendor; and Manage site quality, including direct supervision of project Clinical Research Associates and monitoring deliverables. Qualifications Bachelor’s degree in a health or life science-related field; Advanced degree in a health or life science-related field preferred; At least 2 years of clinical trial management experience in Asia Pacific region ideally in a CRO environment; Experience in Cardiovascular, Renal, Metabolic or Gastrointestinal related studies required; Excellent communication skills including good written and spoken English; and Flexible, accountable and comfortable in working in a global environment. When you join Medpace, you become part of an innovative team that brings cutting-edge therapies to market while building a meaningful and rewarding career focused on scientific excellence and improving patient outcomes around the world through continuous learning and cross-functional collaboration. Purpose-Driven Work Work alongside physicians, scientists, and industry-leading experts committed to advancing the global development of medical therapeutics through clinical research excellence Collaborative Culture Contribute to an interactive team environment that empowers decision making, creative thinking, and continuous learning through open communication and mutual trust. Leadership throughout Medpace is both accessible and approachable Continuous Growth & Development Office based environment with on-site mentors Defined career paths with clear advancement opportunities Industry renowned onboarding and training programs designed to accelerate professional development Ongoing training and continuous learning opportunities throughout your career An environment that encourages employees to influence change, contribute ideas, and grow quickly Other Employee Benefits Competitive compensation programs that recognize and reward performance Comprehensive health, wellness, retirement, and PTO benefits Office based culture with occasional WFH that provides flexibility for eligible positions after training Company-sponsored social events Please note benefits may vary based on country. What to Expect NextA Medpace team member will review your application and if your profile matches our current needs, you will be contacted for an interview. While we review all applications carefully, we are unable to respond to every applicant, and only candidates selected for interviews will be contacted.Role: Healthcare & Life Sciences - Other,Industry Type: Pharmaceutical & Life Sciences,Department: Healthcare & Life Sciences,Employment Type: Full Time, PermanentRole Category: Healthcare & Life Sciences - OtherEducationUG: Any GraduateKey SkillsCROClinicalPharmacologyPharmaceuticalPharmacovigilanceManagementClinical DevelopmentClinical TrialsScientific WritingICHCommunication SkillsClinical ResearchRegulatory AffairsMedical WritingGCPDrug SafetyWritingMedical AffairsHealthcareMedicalAbout companyMedpace’s dedicated teams serve as an extension of your team – we engage quickly and provide strategic thinking – ensuring start-up times are met, superior quality, and the most efficient delivery of every phase of your clinical trial. Our therapeutic and regulatory experts are committed to streamlining your path to approval so every partnership is designed to create research solutions focused on your critical needs.Company InfoLink:Medpace Clinical Research India websiteAddress:Floor 12, Gen 4/1, Unit No. 1203, Aurum Q Parc, Building Q2, Thane Belapur Road, TTC Industrial Navi Mumbai, Thane, Maharashtra, IndiaBeware of imposters! Naukri.com does not promise a job or an interview in exchange of money. 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Home Jobs in Navi MumbaiIEIL has taken all reasonable steps to ensure that information on this site is authentic. Applicants are advised to research bonafides of advertisers independently. IEIL shall not have any responsibility in this regard. We also recommend that you visit Security Guidelines and Terms and Conditions for more comprehensive information on this aspect.Please note that Naukri will not be responsible for any information you share on the company platform.Connect with usAbout usCareersEmployer homeSitemapCreditsHelp centerSummons/NoticesGrievancesReport issuePrivacy policyTerms & conditionsFraud alertTrust & safetyApply on the goGet real-time job updates on our AppAll trademarks are the property of their respective ownersAll rights reserved © 2026 Info Edge (India) Ltd.Our businesses
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