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Full-time
bachelor degree, postgraduate degree
Posted 1d ago
Apply by Aug 26
~40 hrs/week
Responsibilities
The Associate Director leads a programming and reporting team to design and deploy clinical technology system solutions while managing performance and resource allocation. They are responsible for defining integration architecture, driving process optimization, and ensuring compliance with enterprise standards and regulatory requirements.
Requirements
Candidates must possess a Bachelor's degree with at least 8 years of experience or an advanced degree with 4 years of experience in clinical data programming or engineering. Expert-level proficiency in SQL, Python, SAS, or R and a strong understanding of clinical development processes and regulatory standards are required.
Full job description
Job Description
The Associate Director leads and develops a programming and reporting team - set goals, assign work, coach performance, and manage recruiting/onboarding - while communicating status and risks to leadership and partners. Provide hands-on technical review, solutioning support, enforce SOPs/standards, manage workload and prioritization, track quality and timelines, and drive best practices (code review, reusable components, test automation) and continuous improvement.
Responsibilities
Programming and reporting
Lead design and deployment of clinical technology system solutions (e.g., for EDC, RTSM, and eCOA/ePRO) using programming frameworks and automation tools.
Provide technical oversight for clinical programming, reporting, and data integration across portfolios.
Recommend and implement tools to streamline design, build, and validation processes.
Apply data literacy to design transformation strategies for actionable insights.
Develop advanced reporting solutions (dashboards, listings, visual analytics) with reusable components and role-based access.
Data Engineering
Define and govern integration architecture, including data sources and transformation workflows.
Ensure consistent implementation of enterprise standards and reusable assets.
Monitor and troubleshoot data ingestion and consumption for reliability.
Automate and strengthen data engineering processes to reduce risk and improve efficiency.
Develop robust data models, semantic layers, and curated datasets; enforce quality checks.
Process
Drive process optimization by identifying gaps and implementing improvements.
Translate strategy into clear priorities, roadmaps, and ways of working for assigned domains.
Lead testing strategies for solutions; automate validation and ensure traceability.
Contribute to resource planning and workload distribution across global teams.
Set documentation and audit standards; ensure compliance through rigorous change management.
Lead cross-functional collaboration, meetings, and enterprise-level improvement programs.
Influence adoption of data standards, tools, and automation for better delivery and decision-making.
Provide leadership, coaching, and mentoring to build capabilities and foster a culture of quality and collaboration.
Support release management across environments; align stakeholders, lead UAT, and improve reporting standards.
Partner across teams to turn data and technical findings into clear, actionable recommendations
Act as a reliable partner to GDMS and other cross-functional teams, actively seeking input, aligning on priorities, and closing feedback loops to drive high-quality, coordinated delivery.
People management
Set clear objectives aligned to organizational goals; assign work and set priorities.
Conduct regular check-ins and annual reviews; coach for performance; provide recognition.
Help develop career plans; create growth opportunities and promotion cases; ensure appropriate training and mentoring.
Support recruiting and hiring; manage sensitive employee-relations matters (including separations) in partnership with HR.
Balance workloads to support value-added work and work–life sustainability; anticipate obstacles and adjust plans.
Coordinate contingent resources across geographies; ensure role clarity and effective handoffs.
Support management of an operating budget and optimize spend against priorities.
Align teams around a clear direction; facilitate team/functional meetings.
Embrace Enterprise Leadership Skills principles and serve as a role model to their team
Drive enterprise leadership skills in the team
Champions organizational change; drives adoption of new operating models and digital capabilities across global functions
Support staff in the resolution of operational challenges through direct engagement, facilitation, mentoring, and strong problem-solving techniques.
Technical Skills
Expert-level proficiency in different technology languages (e.g., SQL, Python, SAS, and R) for implementing clinical data collectors, integrations, transformations, and visualizations
Evidence of experience in architecting and interoperability of EDC platforms, data integration environments, clinical operations systems, and cloud computing platforms
Proficiency with key data-management and/or clinical operations tools and platforms (e.g., systems for data capture, review, visualization, reconciliation, and reporting), with the ability to help select, configure, or optimize solutions.
Broad understanding of the data-management technology ecosystem (e.g., data capture, review, reconciliation, reporting, analytics, and enabling tools) and how components fit together across the end-to-end process.
Experience leveraging automation, scripting, or digital solutions to streamline data-management activities and reduce manual effort.
Ability to interpret operational and quality metrics, use analytical/forecasting tools for capacity and scenario planning, and translate insights into clear decisions and actions.
Strong understanding of common clinical and regulatory data standards, clinical operational data models, metadata management, and controlled terminologies (e.g., MedDRA, WHODrug) to ensure consistency and submission readiness.
Strong understanding of validation, system lifecycle, data privacy, and System Development Lifecycle Management activities
Strong understanding of drug discovery process, FDA regulations, GxP / ICH guidelines
Ability to connect business outcomes to technical deliverables
Soft Skills
Strong ability to lead teams in a matrixed, global organization while ensuring delivery excellence through effective problem-solving techniques
Demonstrated success in coaching, developing, and performance-managing high-performing individuals
Builds strong partnerships across technical, business, and quality functions to enhance collaboration and deliver integrated outcomes
Balances business needs, resource capacity, and compliance requirements to make sound operational decisions
Capable of leading teams through process and organizational transformation with empathy and clarity
Education
Bachelor of Arts / Sciences with a minimum of 8 years' experience in clinical data programming, data engineering, or related data-management/clinical operations functions, including a minimum of 2 years of people management experience.
or
Advanced Degree (master's or doctorate) with a minimum of 4 years' experience in clinical data programming, data engineering, or related data-management/clinical operations functions, including a minimum of 2 years of people management experience.
Demonstrated deep SME skills in clinical development.
Advanced English level: Proficient in English
Required Skills:
Adaptability, Clinical Data Management, Clinical Trials, Data Analysis, Data Extraction, Data Integration, Data Validation, Decision Making, Good Clinical Practice (GCP), Interpersonal Relationships, People Leadership, Pharmacovigilance, PL/SQL (Programming Language), Regulatory Compliance, Strategic Thinking
Search Firm Representatives Please Read Carefully Merck & Co., Inc., Rahway, NJ, USA, also known as Merck Sharp & Dohme LLC, Rahway, NJ, USA, does not accept unsolicited assistance from search firms for employment opportunities. All CVs / resumes submitted by search firms to any employee at our company without a valid written search agreement in place for this position will be deemed the sole property of our company. No fee will be paid in the event a candidate is hired by our company as a result of an agency referral where no pre-existing agreement is in place. Where agency agreements are in place, introductions are position specific. Please, no phone calls or emails.
Employee Status:
Regular
Relocation:
No relocation
VISA Sponsorship:
No
Travel Requirements:
No Travel Required
Flexible Work Arrangements:
Hybrid
Shift:
Not Indicated
Valid Driving License:
No
Hazardous Material(s):
N/A
Job Posting End Date:
08/26/2026
*A job posting is effective until 11:59:59PM on the day BEFORE the listed job posting end date. Please ensure you apply to a job posting no later than the day BEFORE the job posting end date.
Related keywords
Data ArchitectureClinical ProgrammingEDCRTSMeCOAePROData EngineeringSQLPythonSASRCloud ComputingMedDRAWHODrugGxPICH Guidelines
At MSD, known as Merck & Co., Inc., Rahway, NJ, USA in the United States and Canada, we are unified around our purpose: We use the power of leading-edge science to save and improve lives around the world. For more than 130 years, we have brought hope to humanity through the development of important medicines and vaccines. We aspire to be the premier research-intensive biopharmaceutical company in the world – and today, we are at the forefront of research to deliver innovative health solutions that advance the prevention and treatment of diseases in people and animals. We foster a diverse and inclusive global workforce and operate responsibly every day to enable a safe, sustainable and healthy future for all people and communities. For more information, visit www.msd.com and connect with us on Facebook, Instagram, Twitter, and YouTube.
Offices: 90 E Scott Ave, Rahway, New Jersey 07065, US · 2000 Galloping Hill Road, Kenilworth, NJ 07033, US · Jalan Puteri 5/20, Puchong, Selangor 47100, MY · Clos du Lynx 5, Woluwe-Saint-Lambert, Brussels Region 1200, BE · Keilaranta 3, Espoo, Southern Finland 02150, FI
Animal FeedVeterinaryHealth CareData ManagementBiopharmaClinical TrialsBiotechnologyMedicalPharmaceuticalData Center Automation
How many Science & Research jobs are open in San José, Costa Rica right now?
There are currently 39 open science & research positions in San José, Costa Rica listed on Clera. New openings are added daily as companies post roles.
Which companies are hiring for Science & Research roles in San José, Costa Rica?
Companies currently hiring include Grupo Dökka, MSD, Fortrea, Lonza, Roche, among others. Browse the listings above to see every active employer.
Are there remote or hybrid Science & Research jobs in San José, Costa Rica?
Yes — 20 of the 39 open science & research positions offer remote or hybrid work (6 remote, 14 hybrid).
How do I apply for Science & Research jobs in San José, Costa Rica?
Each listing links directly to the employer's application page. Apply early — fresh listings get the most recruiter attention in the first two weeks.