US Patient Enrollment Coordinator (Evening Shift)

Job DescriptionMinerva Research Solutions is a clinical trial management service provider. We aim to transform the landscape of healthcare and research with our quality clinical services. We support the biotech, medical, and pharma industries through all phases of the clinical trial lifecycle. Our services include Data Operation, Recruitment Services, and Regulatory. Our goal is to speed up the lifecycle of novel therapies through streamlined processes, stringent timelines & real-time solutions. Our clinical trial support services & consultations are tailored to foster your product and requirements. We aim to deliver high-quality data and solutions to make your clinical trials a success.

We follow stringent FDA and GCP regulations throughout all phases of the clinical trial process. Minerva Research Solution is looking for dynamic individuals in the role of Patient Enrollment Specialist responsible for screening new leads, conducting follow-ups, and documenting participants for assigned active clinical trials. This specialist contributes significantly to clinical trials by building a comprehensive database in the Clinical Trial Management System (CTMS) of willing and qualified study volunteers. Industry: Information Technology & ServicesHospital & Health CareClinical-Trials and Research IndustryKey Responsibilities:

Conduct phone interviews and screenings for prospective clinical study participants in USMaintain an organized database of clinical study participantsDevelop outreach strategies to enhance participant recruitmentInteract directly with study participants via phone calls, SMS, etcCollaborate with Medical Staff (CRCs) to ensure adequate subject recruitment for each studyEnhance and maintain study documentation and volunteer records, including consent formsAssist in sales, marketing, and outreach efforts as neededProvide accurate study-related information to participants in USCultivate a safe, positive, and fast-paced work environmentUndertake other related duties and participate in special projects as assignedBehavioral Competencies:

Conceptual capability, problem-solving, and decision-making abilityStrong commitment to teamwork, work ethics, and etiquetteEffective planning and organizing skills with priority settingProactive knowledge and information sharing within the teamCustomer-focused with strong communication skillsActive learning attitude with a continuous improvement mindsetMinimum Qualifications: Essential: Bachelor’s Degree in BDS, Pharm-DGood knowledge of Clinical TrialsComputer literate with good knowledge of MS OfficeProficiency in the English language written and spoken both. (MANDATORY)Therapeutic Communication in English with US accent is preferred6 months to 1 year experience in a relevant fieldBenefits:

Competitive salary and performance-based bonusesQuarterly Bonus StructureMedical health insurance coverage for you and your family (Spouse & Children)Employees Old-age benefits coverage40-hours WeekExposure to US MarketProfessional learning and development supportGenerous vacation and paid time offEmployee assistance programs for mental healthCompany-sponsored events and team-building activitiesDiverse, professional and inclusive work environmentOpportunities for career growthCutting-edge technology and toolsFamily-friendly policies, including parental leaveCommuter benefits or transportation assistanceSocial responsibility and community involvement programsOpenings: Equal opportunity employersFull-timeOn-site job (Night shift)Work Schedule Timings:

Monday to Friday6PM to 2AM (transport facility provided for female staff only and allowance for male employees, additional night shift allowance)Powered by JazzHRPnwRHA2y1l