Job description
Clinical Research Associate Entry Posted by Firm in Medical Services Domain 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 Research Associate EntryMedpace Clinical Research India4.213 Reviews0 - 1 yearsNot DisclosedNavi MumbaiPosted: 1 week agoApplicants: 100+Clinical Research Associate EntryMedpace Clinical Research India4.213 ReviewsJob description TitleOur successful Clinical Research Associates possess varied backgrounds in medical and other science-related healthcare fields. Individuals who have succeeded in the CRA role include: Nurses Dieticians Pharmacy Technicians Pharmaceutical/Device Sales Representatives Biotech Engineers PhD/Pharm.D candidates Health and Wellness Coordinators Research Assistants. PACE® – MEDPACE CRA TRAINING PROGRAMNo research experience is needed as 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. UNEXPECTED REWARDS This role takes you on a journey through travel and excitement which will allow you to make a difference on a large scale through the enhancement of pharmaceuticals and medical devices. The CRA position provides many other distinctive advantages including: Dynamic working environment, with varying responsibilities day-to day Expansive experience in multiple therapeutic areas Work within a team of therapeutic and regulatory experts Defined CRA promotion and growth ladder with potential for mentoring and management advancements Competitive pay and opportunity for significant travel bonus 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. ResponsibilitiesAs a CRA Entry, you will specifically be responsible for the following: Conduct 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, including facilities, laboratories, equipment, and staff; Medical record and research source documentation verification against case report form data, including informing the site staff of any entry errors, ensuring good documentation practices are being adhered to and communicating protocol deviations appropriately per SOPs, GCP and applicable regulatory requirements; 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, serious adverse events, concomitant medications and corresponding illnesses to confirm accurate data reporting in accordance with the protocol; Assessing the clinical research site’s patient recruitment and retention success and offering suggestions for improvement; Completion of monitoring reports and follow-up letters, which includes providing summaries of the significant findings, deviations, deficiencies, and recommended actions to secure compliance. Qualifications Minimum of a bachelor’s degree; Health or life science related field preferred; Candidate with Clinical Research Coordinator experience is an advantage: Willing to travel approximately 60-80% nationally; Familiarity with Microsoft® Office; and Strong communication and presentation skills a plus. 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: Pharmaceutical & Biotechnology - Other,Industry Type: Pharmaceutical & Life Sciences,Department: Research & Development,Employment Type: Full Time, PermanentRole Category: Pharmaceutical & BiotechnologyEducationUG: Any GraduateKey SkillsDrugCROBiotechnologyClinicalScienceOncologyPharmaceuticalResearchClinical DevelopmentMS OfficeClinical TrialsRecruitmentPresentation SkillsCommunication SkillsCRAClinical ResearchGCPPharmacyRegulatory RequirementsHealthcareMedicalMonitoringAbout 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. Fraudsters may ask you to pay in the pretext of registration fee, Refundable Fee…Read moreSimilar jobsExperienced Clinical Research AssociateMedpace Clinical Research India4.213 reviewsNavi MumbaiDrugCROBiotechnologyClinicalOncologyPharmaceuticalPharmacovigilanceResearchClinical DevelopmentMS OfficeClinical TrialsRecruitmentPresentation SkillsCommunication SkillsCRAClinical ResearchGCPPharmacyRegulatory RequirementsHealthcareMedicalMonitoringRegulatoryMicrosoftDevelopmentPosted 13 Days AgoClinical Research AssociateAirvin Skills2.25 reviewsHyderabad, Chennai, BengaluruLife SciencesClinical ResearchPharmaceutical SciencesClinical OperationsClinicalPharmaceuticalResearchPharmacovigilanceClinical TrialsICH-GCPData QualityCRAMedical WritingPharmacyHealthcareMedical AffairsMedicalClinical Data ManagementWritingQualityPosted 12 Days AgoClinical Research Associate Leading CRO PuneHiring for - Leading Clinical Research Organizatio...Posted by Hindco Recruitment ConsultantsPimpri-Chinchwad, Pune, Mumbai (All Areas)Clinical TrialsLife SciencesCRAClinical ResearchClinical Research AssociateDrugBiotechnologyMedDRAPSURClinical OperationsClinicalProceduresPharmacologyPharmacovigilanceMedicineDrug SafetyCase ProcessingClinical Data ManagementArgusOracle ArgusPosted 21 Days AgoClinical Research CoordinatorAirvin Skills2.25 reviewsHybrid - Hyderabad, Chennai, BengaluruClinical OperationsClinical ResearchClinical Data ManagementClinical DatabaseClinicalBiochemistryClinical DevelopmentPharmacovigilanceClinical TrialsClinical PharmacyClinical MonitoringPharmacyDrug SafetyClinical DocumentationClinical DataDrugDataOperationsPosted 25 Days AgoClinical Research AssociateWOW SoftechPosted by WOW SoftechRemoteon- site monitoringCRAClinical ResearchGlobal Clinical trialsClinical Data ManagementClinical TrialsClinicalData managementSitePosted 15 Days AgoRoles from top companiesMicrobiology Quality Control Exec.Firm in Medical Services Domain0-1 Yrs1-2 Lacs P.A.BengaluruHiring for one of these companies3d agoMicrobiologistLeading Content Development MNC0-1 Yrs50,000 P.A.Noida, Dehradun, ChennaiHiring for one of these companies3d agoRegister to unlockJobs you might be interested inPharmacovigilance Associate -Pharmacy / BDS / Life SciencesClininfotech4.39 reviewsHyderabad(Ameerpet), Pune(Shiva Nagar), Be...Posted 26 Days AgoWanted Pharmacovigilance Assistant -MaduraiResolve Medicode3.63 reviewsMadurai(Arapalayam +2), Dindigul, TheniPosted 5 Days AgoClinical Trial AssistantAirvin Skills2.25 reviewsHybrid - Visakhapatnam, Hyderabad, Bengalu...Posted 12 Days AgoDrug Safety AssociateAirvin Skills2.25 reviewsHybrid - Hyderabad, Chennai, BengaluruPosted 12 Days AgoClinical Research CoordinatorAirvin Skills2.25 reviewsHyderabad, Coimbatore, BengaluruPosted 12 Days AgoSalary insightsClinical Research Associate in Medpace Clinical Research India typically earns between₹5.6 - ₹8.2 L/yrSee detailed salary breakupPowered by Recommended for youKnow moreAI-enhanced profileGet noticed by recruiters by increasing profile views upto 3 timesNaukri Pro builds an AI enhanced profile and keeps it active in searches. 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
Role details
Beware of job fraudJeevika India never asks candidates to pay for a job or interview. Read safety details
Warning signs
- Requests for registration, interview, security, training or refundable fees.
- Requests for OTPs, passwords, card details or bank-account credentials.
- Instant selection or an offer letter without a proper interview.
- Unrealistic salary promises or pressure to act immediately.
- Messages from unofficial domains, personal emails or unknown numbers.
- Requests to communicate or pay outside the employer’s verified process.
- Requests to install unknown applications, screen-sharing tools or remote-access software.
- Recruiters using look-alike domains, misspelled company names or unverifiable profiles.
- Requests to purchase equipment, courses or documents from a specified person.
Protect yourself
- Independently verify the employer, recruiter and job information.
- Check the company’s official website, address and contact details before responding.
- Confirm important communication through an official company email domain.
- Request a written job description and carefully review every offer condition.
- Never transfer money to obtain an interview, job or offer letter.
- Do not share OTPs, passwords or confidential banking information.
- Never install remote-access software or share your screen with an unknown recruiter.
- Do not hand over original identity, education or employment documents.
- Share identity documents only after verification and add the intended purpose where appropriate.
- Keep copies of suspicious emails, messages, numbers and payment requests.
Disclaimer: Company names, trademarks and logos belong to their respective owners and are displayed for identification and informational purposes. Jeevika India takes reasonable steps to present useful job information, but candidates must independently verify every employer, recruiter and opportunity before applying. Jeevika India does not guarantee interviews, selection, employment, salary, job offers or the accuracy of information supplied by third parties, and is not responsible for payments, losses or communications made outside Jeevika India.