Associate Specialist, Clinical Data Management

Job DescriptionPrimary activities include, but are not limited to:Assumes the responsibilities for all clinical programming (including reporting and analytics) deliverables including Oracle, Veeva platforms along with the external data captured in support of the clinical studies.  Coordinates and participates in the following activities:Design, build, maintain, test, and document data review based on written specifications established by Global Clinical Data Management, Clinical Research and Global Safety.  Review the technical feasibility of study team proposed programming/reporting and technically implements them. Work effectively among   team to communicate issues and ideas to improve the business along with understanding of Protocol .Support the development & reporting for data cleaning, medical review, clinical monitoring, and safety reports for quality and timely availability in support of our customer needs.  Perform ongoing support for In-Life Reports.  Change Requests and Incident Reports are fully documented, signed off, tracked, and reported to upper management.  ​Participate in extra activities including, but not limited to, study improvement task forces, automations, initiatives, testing of new systems, and ongoing training and mentoring.Education: B.A. or B.S. degree, preferably in mathematics, science, a healthcare-related discipline, or computer science; or relevant Pharma skills and experience.Knowledge and Skills: Expected to have a good technical proficiency in a Clinical Data Management/Reporting Systems like PowerBI or SQL/PL SQL or Databricks or Python or SAS, etc along with AI related tools. Solid knowledge of MS Windows/Office software and exposure to web-based applications.Solid knowledge of System Development Lifecycle Management / system validation knowledge Ability to establish and maintain good working relationships with different functional areas.Strong sense of urgency and customer focus.Possesses excellent communication skills and interacts effectively with Study Team aling with Strong organizational and problem-solving skills.Desire and ability to learn new processes and technologiesAbility to multi-task, work independently, and good communication skillsUnderstanding of drug discovery process, FDA regulations, GxP guidelines, ICHclinicaltrialjobs  EligibleforERP#GDMSMSJR Required Skills: Adaptability, Adaptability, Analytical Problem Solving, Clinical Data Cleaning, Clinical Data Management, Clinical Medicine, Clinical Physiology, Clinical Reporting, Clinical Research, Computer Science, Data Analysis, Data Documentation, Data Entry, Data Processing, Data Reporting, Data Review, Data Validation, Data Visualization, Drug Discovery Process, FDA Regulations, Good Clinical Practice (GCP), Medical Review, Nephrology, Pathophysiology, Root Cause Analysis (RCA) {+ 2 more}Preferred Skills: Current Employees apply HERECurrent Contingent Workers apply HEREUS and Puerto Rico Residents Only:Our company is committed to inclusion, ensuring that candidates can engage in a hiring process that exhibits their true capabilities. Please click here if you need an accommodation during the application or hiring process.As an Equal Employment Opportunity Employer, we provide equal opportunities to all employees and applicants for employment and prohibit discrimination on the basis of race, color, age, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability status, or other applicable legally protected characteristics.  As a federal contractor, we comply with all affirmative action requirements for protected veterans and individuals with disabilities.  For more information about personal rights under the U.S. Equal Opportunity Employment laws, visit:EEOC Know Your RightsEEOC GINA Supplement​We are proud to be a company that embraces the value of bringing together, talented, and committed people with diverse experiences, perspectives, skills and backgrounds. The fastest way to breakthrough innovation is when people with diverse ideas, broad experiences, backgrounds, and skills come together in an inclusive environment. We encourage our colleagues to respectfully challenge one another’s thinking and approach problems collectively.Learn more about your rights, including under California, Colorado and other US State ActsThe salary range for this role is$71,900.00 - $113,200.00This is the lowest to highest salary we in good faith believe we would pay for this role at the time of this posting. An employee’s position within the salary range will be based on several factors including, but not limited to relevant education, qualifications, certifications, experience, skills, geographic location, government requirements, and business or organizational needs.The successful candidate will be eligible for annual bonus and long-term incentive, if applicable.We offer a comprehensive package of benefits.  Available benefits include medical, dental, vision healthcare and other insurance benefits (for employee and family), retirement benefits, including 401(k), paid holidays, vacation, and compassionate and sick days. More information about benefits is available at https://jobs.merck.com/us/en/compensation-and-benefits.You can apply for this role through https://jobs.merck.com/us/en (or via the Workday Jobs Hub if you are a current employee). The application deadline for this position is stated on this posting.San Francisco Residents Only: We will consider qualified applicants with arrest and conviction records for employment in compliance with the San Francisco Fair Chance OrdinanceLos Angeles Residents Only: We will consider for employment all qualified applicants, including those with criminal histories, in a manner consistent with the requirements of applicable state and local laws, including the City of Los Angeles’ Fair Chance Initiative for Hiring OrdinanceSearch Firm Representatives Please Read Carefully Merck & Co., Inc., Rahway, NJ, USA, a