Role Description Nos encontramos en la búsqueda para la vacante de Oficial de Admisiones Online. La vacante es dirigida a una institución universitaria, el oficial de admisiones será responsable de orientar y dar seguimiento a prospectos desde el proceso inicial de admisión hasta la formalización de matrícula. La persona seleccionada deberá brindar un servicio de excelencia, asegurar el cumplimiento de requisitos establecidos y contribuir al logro de las metas institucionales de reclutamiento y nuevo ingreso. - Orientar a prospectos y solicitantes sobre programas académicos, requisitos y procesos de admisión. - Dar seguimiento continuo a estudiantes interesados hasta completar el proceso de matrícula. - Mantener comunicación constante mediante llamadas, correos electrónicos y plataformas digitales. - Recibir, evaluar y procesar solicitudes de admisión. - Preparar informes y cumplir con las metas establecidas por la institución. - Cumplir con las políticas y procedimientos institucionales. Qualifications - Experiencia en servicio al cliente. - Experiencia en procesos administrativos, admisiones o reclutamiento (preferible). - Experiencia trabajando con estudiantes o público general. - Experiencia en ventas y orientación de manera telefónica. - Grado Asociado en Administración de Empresas o áreas relacionadas (preferiblemente). Requirements - Dominio básico de computadoras y plataformas digitales. - Excelentes destrezas de comunicación oral y escrita. - Capacidad para trabajar bajo presión y por metas. - Organización y manejo de múltiples tareas. - Habilidad para establecer relaciones interpersonales efectivas. - Manejo confidencial de información. Benefits - Salario: $12.00 por hora. - Incentivo adicional de $50.00 para telefonía e internet. - Turnos rotativos de lunes a viernes. - Sábados alternos. - Disponibilidad para trabajar entre 9:00 a.m. y 9:00 p.m. - Modalidad Online- Remoto.

Role Description - Learn from Pilot-in-Command’s experience, training and instruction. - Assist Pilot-in-Command in operation of the aircraft as delegated by Pilot-in-Command, and operate within the provisions of the FCOM and FCTM. - Assist Pilot-in-Command before, during, and after each flight to include pre-flight walk-around, and at conclusion assist in completing necessary reports/maintenance discrepancies. - Validate all required charts, approach plates and other navigational publications are current and aboard the aircraft prior to the cockpit preflight. - Delegate duties only when the Pilot-in-Command becomes incapacitated, and then assume duties of the Pilot-in-Command. Qualifications - Minimum 2,000 hours Total Time. - Minimum 500 hours Pilot-in-Command. - Minimum 500 hours Multi-Engine Land. - Must hold FAA First Class Medical and FCC Radio License. - Must hold FAA Unrestricted ATP with Multi-Engine and Instrument ratings, and be able to obtain PIC rating of assigned aircraft at conclusion of new hire or transition training. - Must be legally authorized to work in the United States for any employer without sponsorship. - Must have a valid passport, and the ability to travel internationally to all countries Omni requires. - Must be able to pass a 10-year Background/Criminal History Records Check and pre-employment drug screen. - Must be 23 years of age or older. - Must be able to read, write, speak, and understand the English Language. - Ability to work varying hours of the day or night, on weekends and holidays. - Must be able to secure appropriate airport authority and security badges. - Excellent communication skills and quick and accurate decision-making with close attention to detail. - Flying in the last 12 months. Requirements - High school diploma or GED required. - College degree preferred. - Must be able to obtain First Class Medical Certificate. - Travel 100%. - Lift up to 60 lbs. Mental Capability Requirements - Able and willing to work in a culturally diverse atmosphere and professionally interact with passengers and crew under stressful conditions. - Must be willing to work in a time-sensitive environment and effectively handle stress associated with meeting deadlines, and managing unexpected change. - Capable of interpreting a variety of and multiple instructions furnished in written, oral, diagram, or schedule form. - Ability to communicate effectively so to be understood. - Must be able to remain calm, think and react quickly in all types of emergency situations including but not limited to: medical emergencies, aircraft decompression, emergency evacuations, fires, security threats, passenger disturbances, turbulence, etc. - Able to process information quickly. - Ability to complete routine forms, use existing form letters and/or conduct routine oral communication. - Possess attention to detail. Company Description Drug Free Workplace, Equal Opportunity Employer M/F/Disability/Veterans/VEVRAA Federal Contractor/Sexual Orientation/Gender Identity. We are an equal employment opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, gender, national origin, disability status, protected veteran status or any other characteristic protected by law. Military and civilian service alumni are encouraged to apply.

Role Description We are looking for a Proactive PV Officer and/or Senior PV Officer to work within the Clinigen Lifecycle Services team and will be dedicated to one or more of our pharmaceutical clients with a truly global presence supporting the collation, processing and analysis of safety information on behalf of a Client(s) product(s); this unique industry-changing relationship redefines collaboration. This role requires you to be a passionate pharmacovigilance professional, who is a dedicated and enthusiastic team player, that wants to work with a new business that strives to gain and maintain an exceptional reputation as a PV Service Provider that is knowledgeable, cares and produces high quality work. We are looking for applicants based in Malaysia and Croatia. Applicants based in EU and South Africa are also welcome. Key Responsibilities: - Working within the Pharmacovigilance Operations team - Assess and process serious adverse events (SAEs) and Individual Case Safety Reports (ICSRs) into the Global Drug Safety database - Support quality and efficiency strategies within the organisation - Assisting in departmental regulatory inspection preparedness for the company pharmacovigilance system and actively participating in PV inspections or audits as required - Contributes to improvements of team processes - Other PV operational activities or initiatives as assigned - Maintaining good client relations and ensuring a consistently high quality of work for each client - Review of Medical Information Enquiries and Product Quality Complaints to ensure all safety information has been captured For the Clients: - Managing mailboxes – responding to data entry / case processing queries from Clients and Client Partners, providing responses - Triage, tracking and forwarding of safety data from client Managed Access Programmes - Distribution of SUSARs to enrolled physicians within MAP as per agreement with client - Case processing of SAEs and/or ICSRs - Case regulatory reporting; preparing relevant cases for submission and sending to the relevant Regulatory Authorities - Working on E2B/R3 format reporting and Case Finalization; reading error messages and taking steps to correct cases as a result of negative acknowledgments - Supporting investigation of cases of non-compliance of SAEs/ICSRs - Performing Literature Article reviews - Performing follow-up related to queries and requests regarding case handling - Communicating with Clients and/Partners regarding the evaluation and processing of ICSRs - Performing quality-control of cases in the Global Drug Safety database - Performing reconciliation activities as per Client contracts and each Client Operating Guideline (COG) - Assists when required in Partner, Health Authority Audits/Inspections - Participation in Client audits and inspections Additional Duties - The list of duties is not intended to be exhaustive, but gives a general indication of the tasks involved - Support the collation and dissemination of quality and compliance metrics for pharmacovigilance and medical information activities - It is the nature of the company that tasks and responsibilities are, in many circumstances, unpredictable and varied. All employees are, therefore, expected to work in a flexible way when the occasion arises and acknowledge that tasks not specifically covered in their job description are not excluded Qualifications - Healthcare Professional qualification or equivalent of a Bachelor of Science (BSc) degree - Evidence of being able to build relationships with key internal and external customers and demonstrate customer focus - Attention to detail and the ability to work effectively in an environment characterised by tight timelines and changing priorities - Excellent organizational and prioritization skills and strong analytical / problem solving skills - Excellent oral and written communication skills - Ability to build relationships with key internal and external customers - Excellent attention to detail and ability to work under pressure - Extensive knowledge of MS Office Applications and systems - Outstanding written, verbal, and interpersonal communication skills - Excellent ability to handle multiple tasks in a fast-paced and constantly changing environment - Proven ability to work collaboratively within a matrix and/or cross-functional environment - Self-motivated and organised, with the ability to work unsupervised for periods of time - Excellent analytical thinking, with the ability to evaluate and present complex safety data applying sound judgement Benefits - 27 days, plus bank holidays - Discretionary Bonus - Pension contributions & Life Assurance scheme - Annual salary review - Enhanced Employee Assistance Programme - Long service awards - Recognition scheme & employee of the year awards

Role Description We are looking for a Proactive PV Officer and/or Senior PV Officer to work within the Clinigen Lifecycle Services team and will be dedicated to one or more of our pharmaceutical clients with a truly global presence supporting the collation, processing and analysis of safety information on behalf of a Client(s) product(s); this unique industry-changing relationship redefines collaboration. This role requires you to be a passionate pharmacovigilance professional, who is a dedicated and enthusiastic team player, that wants to work with a new business that strives to gain and maintain an exceptional reputation as a PV Service Provider that is knowledgeable, cares and produces high quality work. Key Responsibilities: - Working within the Pharmacovigilance Operations team - Assess and process serious adverse events (SAEs) and Individual Case Safety Reports (ICSRs) into the Global Drug Safety database - Support quality and efficiency strategies within the organisation - Assisting in departmental regulatory inspection preparedness for the company pharmacovigilance system and actively participating in PV inspections or audits as required - Contributes to improvements of team processes - Other PV operational activities or initiatives as assigned - Maintaining good client relations and ensuring a consistently high quality of work for each client - Review of Medical Information Enquiries and Product Quality Complaints to ensure all safety information has been captured For the Clients: - Managing mailboxes – responding to data entry / case processing queries from Clients and Client Partners, providing responses - Triage, tracking and forwarding of safety data from client Managed Access Programmes - Distribution of SUSARs to enrolled physicians within MAP as per agreement with client - Case processing of SAEs and/or ICSRs - Case regulatory reporting; preparing relevant cases for submission and sending to the relevant Regulatory Authorities - Working on E2B/R3 format reporting and Case Finalization; reading error messages and taking steps to correct cases as a result of negative acknowledgments - Supporting investigation of cases of non-compliance of SAEs/ICSRs - Performing Literature Article reviews - Performing follow-up related to queries and requests regarding case handling - Communicating with Clients and/Partners regarding the evaluation and processing of ICSRs - Performing quality-control of cases in the Global Drug Safety database - Performing reconciliation activities as per Client contracts and each Client Operating Guideline (COG) - Assists when required in Partner, Health Authority Audits/Inspections - Participation in Client audits and inspections Additional Duties: - The list of duties is not intended to be exhaustive, but gives a general indication of the tasks involved - Support the collation and dissemination of quality and compliance metrics for pharmacovigilance and medical information activities - It is the nature of the company that tasks and responsibilities are, in many circumstances, unpredictable and varied. All employees are, therefore, expected to work in a flexible way when the occasion arises and acknowledge that tasks not specifically covered in their job description are not excluded Qualifications - Healthcare Professional qualification or equivalent of a Bachelor of Science (BSc) degree - Evidence of being able to build relationships with key internal and external customers and demonstrate customer focus - Attention to detail and the ability to work effectively in an environment characterised by tight timelines and changing priorities - Excellent organizational and prioritization skills and strong analytical / problem solving skills - Excellent oral and written communication skills - Ability to build relationships with key internal and external customers - Excellent attention to detail and ability to work under pressure - Extensive knowledge of MS Office Applications and systems - Outstanding written, verbal, and interpersonal communication skills - Excellent ability to handle multiple tasks in a fast-paced and constantly changing environment - Proven ability to work collaboratively within a matrix and/or cross-functional environment - Self-motivated and organised, with the ability to work unsupervised for periods of time - Excellent analytical thinking, with the ability to evaluate and present complex safety data applying sound judgement Benefits - 27 days, plus bank holidays - Discretionary Bonus - Pension contributions & Life Assurance scheme - Annual salary review - Enhanced Employee Assistance Programme - Long service awards - Recognition scheme & employee of the year awards