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experience)","content":"**Senior Clinical Research Associate** **(Level dependent on experience)**\n**Please submit your CV in English for Quickest Review Process!**\n \n\nMaintaining our company culture across all regions, and especially with our remote employees, is incredibly important to our overall success. To do so, we have weekly all\\-staff meetings in which each department can provide an update on a study or milestone that they have achieved. Each employee also has the opportunity join one of our CTI Cares committees that not only help support our culture, but also focus on our various philanthropic efforts. \n\n \n\n**What You'll Do**\n* Serve as main CTI contact for assigned study sites\n* Conduct site visits (pre\\-study \\[PSV], site initiation \\[SIV], interim monitoring \\[IMV], and close\\-out \\[COV]) and complete site visit deliverables with quality and within given timelines in Monitoring Plan while adhering to all applicable regulatory requirements, SOPs and ICH GCP\n* Assist with or oversee study start\\-up activities, including feasibility, pre\\-study activities and site selection\n* Collect, review and track essential/regulatory documents\n* Participate in and complete all general and study specific training as required\n* Participate in investigator, client and project team meetings; may include presentations\n* Create and implement subject enrollment strategies for assigned study sites\n* Ensure proper storage, dispensation and accountability of all Investigational Product (IP) and trial\\-related materials\n* Perform site management activities and provide ongoing updates of site status to Clinical Project Manager\n* Conduct remote monitoring and complete related activities in accordance with study specific Monitoring Plan\n* Utilize systems and reports to track subject status, subject case report form (CRF) retrieval / source document review (SDV), regulatory documents, and IP\n* Assist with project\\-specific activities as member of Project Team\n* Participate in the development of CRFs and other study related documents (subject worksheets, Monitoring Plan, etc.)\n* Perform translation, customization, and review of Patient Information sheet and Informed Consent, protocol synopsis and other study applicable documents as per required procedures\n* Where applicable, provide support to Regulatory Affairs Study Start\\-up Team in the preparation or revision of documentation for submission to Ethics Committee(s), Institutions Ethics Committees, Regulatory Authorities, Competent Authorities or Institutions Administration Boards, and follow\\-up the evaluation process until approval is available. 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teams and other stakeholders to gather feedback on Center performance, and in collaboration with the Service Owner, develop actions as necessaryLiaise closely with managers across the NBI department, gaining an understanding of wider team activities such as ConflictsCoordinate activities with system vendors, providing regular feedback, documenting requirements or raising issues where necessary to ensure operational and process effectivenessUpdate and create policies, procedures, and standards as requirements change or as a result of other trigger eventsPromote the Firm values of collaboration and a culture of friendship amongst the teamBuild trusted relationships with key internal stakeholders: Partners, PAs, local AML Compliance Managers, NBI management, displaying SME knowledge and acting as a key contact for AML/KYC queries/topicsAct as a point of contact for internal testing and audit requirementsCollaborate with management and counterparts across other Centers to deliver team 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Program & Project Management in Ensenada
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Program & Project Management
Ensenada
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Location:Ensenada
Category:Program & Project Management
Senior Clinical Research Associate (level dependent on experience)63836781534849120
Indeed
Senior Clinical Research Associate (level dependent on experience)
**Senior Clinical Research Associate** **(Level dependent on experience)** **Please submit your CV in English for Quickest Review Process!** Maintaining our company culture across all regions, and especially with our remote employees, is incredibly important to our overall success. To do so, we have weekly all\-staff meetings in which each department can provide an update on a study or milestone that they have achieved. Each employee also has the opportunity join one of our CTI Cares committees that not only help support our culture, but also focus on our various philanthropic efforts. **What You'll Do** * Serve as main CTI contact for assigned study sites * Conduct site visits (pre\-study \[PSV], site initiation \[SIV], interim monitoring \[IMV], and close\-out \[COV]) and complete site visit deliverables with quality and within given timelines in Monitoring Plan while adhering to all applicable regulatory requirements, SOPs and ICH GCP * Assist with or oversee study start\-up activities, including feasibility, pre\-study activities and site selection * Collect, review and track essential/regulatory documents * Participate in and complete all general and study specific training as required * Participate in investigator, client and project team meetings; may include presentations * Create and implement subject enrollment strategies for assigned study sites * Ensure proper storage, dispensation and accountability of all Investigational Product (IP) and trial\-related materials * Perform site management activities and provide ongoing updates of site status to Clinical Project Manager * Conduct remote monitoring and complete related activities in accordance with study specific Monitoring Plan * Utilize systems and reports to track subject status, subject case report form (CRF) retrieval / source document review (SDV), regulatory documents, and IP * Assist with project\-specific activities as member of Project Team * Participate in the development of CRFs and other study related documents (subject worksheets, Monitoring Plan, etc.) * Perform translation, customization, and review of Patient Information sheet and Informed Consent, protocol synopsis and other study applicable documents as per required procedures * Where applicable, provide support to Regulatory Affairs Study Start\-up Team in the preparation or revision of documentation for submission to Ethics Committee(s), Institutions Ethics Committees, Regulatory Authorities, Competent Authorities or Institutions Administration Boards, and follow\-up the evaluation process until approval is available. Provide regular updates to Sponsor/ Client * Where applicable, support or oversee contract negotiation with study sites, Investigator payments and tracking of site payments * Manage ISF and TMF for all assigned study sites in accordance with SOPs or study\-specific Monitoring Plans * Identify and anticipate site issues and implement corrective and preventive actions or escalate as appropriate * Liaise with Clinical Data Management for data cleaning activities * Serve as mentor / trainer for CRAs; may include conducting training/assessment visits * Function in the role of Lead CRA for assigned project(s) **What You Bring** * 3 years of clinical trial monitoring experience or equivalent experience as determined by CTI Management and Human Resources * Bachelor's Degree or higher in allied health field such as nursing, pharmacy, or health / natural science, or RN with Associate's Degree, or 3\-year Nursing Diploma with at least 2 years clinical nursing experience, or equivalent experience as determined by CTI Management and Human Resources * Previous experience in conducting clinical research studies in hospital setting, pharmaceutical company or CRO **Why CTI?** At CTI, we recognize that our people are what make our company successful. Our work moves medicine forward. For that reason, we treat our team members with the respect they deserve, and our numbers show it: * We support career progression – We believe in promoting from within and we have a structured mentoring program and program for recent graduates to provide the support employees need to move forward * We value education and training – We provide tuition assistance, partner with universities and colleges to create programs in our field, and have a dedicated training department * We value our people \- We have never had a layoff in our three decade history and we guaranteed full pay for our employees during the COVID\-19 shut\-down regardless of the number of hours worked. We support a work\-life balance and the importance of time with family by offering generous vacation time, a hybrid work from home schedule, and paid parental leave. * Our culture is unparalleled – We've received multiple awards recognizing CTI as one of the best places to work in the greater Cincinnati area, as well as one of the top CROs in the industry * We think globally and act locally – With employees across 60 countries, we have global reach but maintain culture and connections to the local communities in which we work. Our CTI Cares Committees are dedicated to ensuring the CTI culture and values translate around the world. * We are looking toward the future – We have had a consistent double\-digit growth rate over the last decade, invest in cutting\-edge technology, and pride ourselves on our average annual retention rate of 95%, which is much higher than many other CROs * Our work makes a difference – We focus our work on treatments for chronically and critically\-ill patients, who are depending on us to bring these life\-changing therapies to market
Juncal 1601-1699, B1820 Lanús, Provincia de Buenos Aires, Argentina
Negotiable Salary
Aml/Kyc* Compliance Manager (*Anti-Money Laundering / Know Your Client)63836772857857121
Indeed
Aml/Kyc* Compliance Manager (*Anti-Money Laundering / Know Your Client)
**Detalles de la oferta** ------------------------- AML/KYC\* Compliance Manager (\*Anti\-Money Laundering / Know your Client)AML/KYC\* Compliance Manager (\*Anti\-Money Laundering / Know your Client)DescriptionThe AML/KYC\* Compliance Manager (\*Anti\-Money Laundering / Know your Client) will effectively manage the AML/KYC teams and operations within the New Business Intake department. The AML/KYC Compliance team is responsible for activities such as AML and Sanctions screening, beneficial ownership research, risk assessment and document verification for new and existing client and matter registrations, as well as ongoing monitoring and periodic review. The role\-holder should provide an efficient and effective service to In\-Market personnel to ensure compliance with ethical, legal and regulatory requirements. This individual will be responsible for managing several AML/KYC staff in the Center, ensuring all team members perform to the highest level and adhere to Firm policies and procedures. Responsibilities: Responsible for AML/KYC service delivery in Centers, ensuring high\-quality output from the Centre teamIn partnership with the AML/KYC Service Owner, develop work management strategies ensuring SLAs and KPIs are maintained, trends are identified, and volumes are managed effectivelyLeverage dashboards and available reporting to maintain daily oversight of requests, measure analyst productivity, assess right first\-time rates, and develop any required actions based on findings.Undertake AML and Sanctions screening, beneficial ownership research, risk assessment, document verification, ongoing monitoring and periodic review where necessary, and guide the team and In\-Market personnel on these topicsMonitor office right first time rates to identify issues, trends or training needs, providing feedback to the Service Owner to allow for follow\-up engagement to mitigate risk and quality issuesDeal directly with In\-Market queries, providing support for more junior members of staffProvide expert guidance about AML/KYC regulations, processes and procedures and collaborate with relevant in\-market teams and team members to ensure understanding and complianceContribute towards AML/KYC process improvement and simplificationEnsure adherence across the team with AML/KYC regulation, policy and guidance and Firm standardsResponsible for the training and development of team members, ensuring training conducted at a Center level is aligned with agreed functional and service processes and proceduresSupport analysts in their roles and support departmental performance and success through technical and critical skills training; identify training needs and work with the team to ensure they have the training and support required to perform competently in their rolesResponsible for new hire activities in the Center, including but not limited to induction activities, recruitment, probationary reviews, updating the Service Owner on progress of eachSupport and contribute towards change management efforts where necessary, for example, policy, business, and/or technology changes or updatesProvision of advice, mentoring and training on compliance with relevant laws, including Anti\-Terrorist Financing/Anti\-Money Laundering/Know Your Client issues, NBI and Firm policies and proceduresWork with the Service Owner to develop and implement quality assurance reviews, ensuring all team members receive constructive feedback with a view to continuous improvement and excellent service deliveryPerformance Management responsibilities are an important aspect of the role; hold regular one\-to\-one meetings with team members and contribute towards performance management; work with peers and the manager to ensure objectives, benchmarks and performance expectations are aligned across the AML/KYC department and are consistently appliedResponsible for personnel and administrative matters, including but not limited to resourcing, overtime, attendance and staff training; coordinate assignments, compile and develop operational reporting and other administrative dutiesProvide feedback to the Service Owner on issues, trends, training needs, enhancements, and support in drafting and actioning any required next stepsMeet regularly with Escalate review teams and other stakeholders to gather feedback on Center performance, and in collaboration with the Service Owner, develop actions as necessaryLiaise closely with managers across the NBI department, gaining an understanding of wider team activities such as ConflictsCoordinate activities with system vendors, providing regular feedback, documenting requirements or raising issues where necessary to ensure operational and process effectivenessUpdate and create policies, procedures, and standards as requirements change or as a result of other trigger eventsPromote the Firm values of collaboration and a culture of friendship amongst the teamBuild trusted relationships with key internal stakeholders: Partners, PAs, local AML Compliance Managers, NBI management, displaying SME knowledge and acting as a key contact for AML/KYC queries/topicsAct as a point of contact for internal testing and audit requirementsCollaborate with management and counterparts across other Centers to deliver team projects and initiatives that are aligned with and contribute towards departmental objectivesAssist with any other AML Compliance related matters or projects as identified and assigned by the AML/KYC Service OwnerSkills and Experience: A bachelor's degree is requiredProven experience of working in a professional services environment within an AML/KYC roleManagement experience with proven ability to build and lead a successful teamAML/KYC SME with a strong knowledge and understanding of AML/CTF/Sanctions regulations and requirements and financial crime risks associated with the range of services in the legal industryExperience with AML/KYC/Due Diligence processes, vendors and systemsStrong communication, collaboration and organizational skills. A self\-starter who can influence decision\-making for the benefit of the service and firmExceptional problem\-solving, critical thinking, and analytical skillsHighly self\-motivated, independent and proactive approachProven ability to multi\-task and work well under pressure, prioritize workloads and work to tight deadlinesPositive approach and able to adopt a solution\-based approach in all aspects of workMust have good knowledge of Microsoft Office applications and other productivity tools (Intapp knowledge is an advantage)Manage processes efficiently, with accuracy and attention to detailAble to contribute ideas for process improvements and adapt easily to a changing environmentFlexible to work a reasonable shift schedule is required \#J\-18808\-Ljbffr **Salario Nominal****:** A convenir **Fuente****:** Jobleads
Roque Sáenz Peña 555, B1879 Quilmes, Provincia de Buenos Aires, Argentina
Negotiable Salary
Popular Citiesactive
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