•Develop professional relationships with national and regional scientific leaders and ensure their access to medical and scientific information on areas of therapeutic interest and our Company's products.•Identify potential investigators for participating in phase II-IV clinical trials.•Support patient enrollment and retention efforts.•Address product or trial-related investigator questions.•Provide areas of interest for Organon and discuss study concepts to assess scientific merit and alignment.•Respond to unsolicited requests for assistance from potential investigators regarding the Organon Investigator.•Maintain current knowledge and understanding of the scientific and clinical environment in Organon's areas of interest.•Direct inquiries outside of scope (e.g., grants) to appropriate Organon resources.•Gain deep insights on disease, therapeutic area, healthcare needs, data gaps and challenges in Puerto Rico.•Participate in scientific advisory board meetings or expert input forums and attend scientific and medical meetings.•Support development of Medical Affairs Plan (MAP) and implementation of its activities.•Provide insights on scientific gaps, ideas and other topics gathered from scientific exchange, to inform MISP areas of interest, development programs, and TA strategy.•Provide on-label or disease state scientific training to company commercial personnel, when requested and where allowed.

•Develop high quality business strategies and plans ensuring their alignment with short-term and long-term objectives.•Lead and motivate subordinates to advance employee engagement develop a high performing managerial team.•Oversee all operations and business activities to ensure they produce the desired results and are consistent with the overall strategy and mission.•Make high-quality investing decisions to advance the business and increase profits.•Enforce adherence to legal guidelines and in-house policies to maintain the company's legality and business ethics.•Review financial and non-financial reports to devise solutions or improvements.•Build trust relations with key partners and stakeholders and act as a point of contact for important shareholders.•Analyze problematic situations and occurrences and provide solutions to ensure company survival and growth.•Maintain a deep knowledge of the markets and industry of the company.

•Through an understanding of the accounts’ population health strategies, serves as the medical account manager, collaborating and coordinating with other MA colleagues and select commercial roles in bringing relevant healthcare solutions to these accounts.•Develops and maintains ongoing professional relationships with KDMs in regional organized health systems, serving as the primary medical contact to ensure access to medical and scientific information on the Merck product portfolios and areas of therapeutic interest, as well as non‐product initiatives and areas of focus (e.g.,quality management, outcomes research).•Partners with the IAM teams to develop strategic account plans and associated medical account plans and then executes on medical activities aligned with the plan.•Serves as the primary resource for market dynamics within territory to fully understand decision makers’ evolving information needs to feed into the ongoing value‐proposition development process.•Leads medical account management and planning with associated MA functions for regional accounts and markets.•Serves as the internal medical subject matter expert for each regional account, enabling strategic assessments and medical account management through a complete and systematic communication process to the rest of USMA.•Builds and develops breadth and depth of relationships with key decision makers and works to understand the account’s population health management goals and needs.•Provides customer insights to headquarters.•Serves as a resource for the Health Systems Executive MAD and other members of managed markets organizations on other relevant strategic planning•Serves as a technical resource for questions raised by regional account management and staff on Our Company Products.•Attends and supports scientific and medical meetings and prepares planned post‐meeting deliverables.•Mentors other team members and serves as a resource for the MA management team on strategic planning.

•Provide scientific and technical leadership to ensure professional and credible relationships with thought leaders and external experts.•Ensure a strong medical and scientific presence for Abbvie in key academic centers by facilitation of research and educational initiatives, while supporting requests for medical and scientific information on products or areas of therapeutic interest.•Support internal team such as sales, marketing and members of the Affiliate Brand Team to develop their scientific and technical expertise through the delivery of scientific updates.•Assist in the initiation, oversight and follow up of assigned clinical studies and medical projects initiated within the TA for which the MSL carries responsibility such as registry/database projects, epidemiological surveys, post-authorization studies. •Act as the point of contact with thought leaders to facilitate investigator initiated study ideas and requests for support to medical teams. •Serve as a point of contact within the MA team for thought leaders and external experts within an assigned geographic area in order to satisfy their needs for scientific knowledge in a therapeutic area and relevant AbbVie medicines, to support their safe, effective and appropriate use. •Deliver credible presentations on scientific matters to physicians, individually or in groups.•Participate in the selection process to identify appropriately qualified thought leaders the company would wish to engage in collaborative efforts - such as potential research collaborations, or educational and advisory roles (Advisory boards, Congress, Symposia, etc.).•Facilitate medical and scientific field intelligence - competitor research and medical strategies, educational activities, and communicate, where appropriate, within the Company. •Provide key thought leaders / external experts and internal medical and clinical teams with scientific and technical support for publications of scientific or medical interest.

•Monitor quality, facilities, employees and data of the investigations at the three research centers located in; (1) San Juan, PR (main site), (2) Guayama, PR, and (3) Santo Domingo, Dominican Republic.•Train, provide support and educate staff on clinical trial conduct, GCP, and study protocols.•Oversee and manage staff workloads and assignments.•Developed a e-database to improve monitoring, communication and collaboration between the three research centers.•Data analysis and reporting.•Develop processes and follow up to all administrative and operational areas.•Collaborate with the finance manager in the preparation and monitoring of the operational budget.•Organize, maintain and coordinate processes aimed at effective follow-up of clinical studies.•Coordinate and ensure that all employees and contractors comply with the training required by law, and the agreements established by the sponsors of clinical studies.•Establish internal administrative and operational controls that result in the maximization of resources, the effectiveness of the processes and control of expenses.•Develop standards and processes to monitor and ensure compliance with the human resources manual and the code of conduct.•Implement new ideas to improve the marketing area.•Meet with monitors at each monitor evaluations and address any issues.•Evaluate new protocols for feasibility.•Perform Intervention addressed to assure appropriate utilization.•Assist in defining and developing clinical research strategy and study protocols.•Lead and execute clinical research studies and programs.•Create and document policies and Standard Operation Procedures (SOPs)•Ensure compliance with GCP, OSHA and SOPs•Work with the quality assurance team to develop corrective action plan to address deficiencies.•Review source documentation for completeness and accuracy.•Lead the troubleshooting process to reach resolution for any problem that arise during the course of the study.

• Manage the yearly Annual Health Assessment Campaign• Organize Meeting & Staff• Established patient and employee support including assessment, counseling, education regarding medications and treatment, lab work, documentation with care plan for diagnosis and administration of treatment procedures.• Monitor Quality of Medical Record (EHRZ, Practice Fusion)• Managed clients cases and records audits process; ensured proper corrections of discrepancies were made and approved; updated information in the systems Administrator.• Contacted clients to follow-up on cases• Health Education Intervention• Ordering referrals and prescriptions• Research, Analyze Data & Organize Data• Provide support to medical offices for issues in electronic records, Innova.md, 5-star program and HEDIS.• Provide in-depth clinical expertise, educate treating physicians, and document clearly and concisely.• Occasional educational interaction with attending physicians at client hospital.• Involved in periodic data audit and analysis to identify areas of compliance and process risk and inefficiency, in order to inform areas where real-time processes require modification and or change• Focused real-time chart reviews with a focus on compliance and physician documentation.• Project based review of charts from hospital clients for purposes of evaluating and explaining variance from expected outcomes.

• Annual Health Assessment.• Implement Quality Program through the clinical staff• Electronic Record Manager. • Perform Home visit for patient’s verification of information and to assess further information to complete the Annual Health Assessment.• Generated monthly reports; gave orientation to employees in relation to medical doctor’s orders for patients’ future treatment.• Develop reporting structure.• Perform Intervention addressed to assure appropriate utilization• Provide support to medical offices for issues in electronic records, Innova.md, 5 star program and HEDIS.• Provide in-depth clinical expertise, educate treating physicians, and document clearly and concisely.• Occasional educational interaction with attending physicians at client hospital.• Involved in periodic data audit and analysis to identify areas of compliance and process risk and inefficiency, in order to inform areas where real-time processes require modification and or change• Focused real-time chart reviews with a focus on compliance and physician documentation.• Project based review of charts from hospital clients for purposes of evaluating and explaining variance from expected outcomes.