Job description Medtek is a data science driven company to support faster drug development and healthcare solutions.It support growing Biotech and Pharma companies. Assist clients with Data Technologies, Data Analysis, Data Mining, CDISC, Visualisation and Regulatory reporting. Support end to end Biostatistics, Programming and Data Management work. ESSENTIAL DUTIES AND RESPONSIBILITIES OF PRINCIPAL STATISTICAL PROGRAMMER- Able to independently Lead statistical programming activities for Phase 2/3 studies Able to multitask and work in a matrix environment 8 years experience in SAS programming and Reporting Able to program and deliver in independently with minimum guidance 6+ year of SDTM/ADaM and TLF Programming experience Able to write specification Independently validate others programs Able to work in multitasking environment and lead studies Proactive, multitask and able to work in matrix environment Pay attention to data and provide daily details Able to work in clinical domain with Clinician, Statistician and Scientist. In-depth knowledge of clinical trial design, statistical analysis, and regulatory guidelines. Strong SAS data manipulation, analysis and reporting skills- with strong output programming experience Development and execution of statistical analysis and reporting deliverables (e.g.safety and efficacy analysis datasets, tables, listings, figures) Provide technical guidance to other statistical programmers, and ensure training and development of team members. SUPERVISORY RESPONSIBILITIES: None EDUCATION/EXPERIENCE/KNOWLEDGE & SKILLS: Education/Experience: Master in Statistics, computer science or analytics field with 7+ year experience Knowledge/Skills: Eight + year of Statistical programming experience Six year of experience with CDISC Two year Experience with SQL programming Experience in CDISC SDTM/ADaM domain Good communication skills Job Type: Full-time Pay: 25-30 Lacs P.A. Schedule: 8 hour shift Application Question(s): Can you write ADaM, SDTM specificaiton and programs ? Experience: statistical programming: 7 years (Required)

Job Description (JD) for a Machine Learning Engineer We are seeking a Machine Learning Engineer to join our team and help build intelligent systems that solve complex real-world problems. The ideal candidate will have strong experience in developing ML models, working with large datasets, and deploying scalable machine learning solutions in production environments. Key Responsibilities : Design, build, and deploy applications that leverage machine learning and LLMs (e.g., GPT, LLaMA, Claude, Mistral) Evaluate and benchmark different LLMs for specific use cases (e.g., summarization, Q&A, code generation, domain-specific reasoning) Implement prompt engineering, fine-tuning, or retrieval-augmented generation (RAG) techniques as needed Develop end-to-end pipelines from data preprocessing to model integration into production systems Collaborate with product, research, and backend teams to build user-facing ML-powered features Write clean, modular, and well-documented Python code Ensure application scalability, reliability, and performance Stay up-to-date with the latest advancements in AI, LLMs, and ML tooling Required Qualifications: Education : Bachelor's or Master's degree in Computer Science, Software Engineering, or a related field 2+ years of experience in Python software development and applied ML. Strong understanding of machine learning principles and workflows.

Medtek Dot AI Pvt limited is a data science consulting company supporting global Pharma and Biotech companies. Our mission is to help Unlock insights and drive innovations using the data collected. We are a team of Biostatistician, Data Managers, Programmer s, Engineers and AI developers. Job Summary: We are seeking a dynamic and detail-oriented HR Technical Recruiter to manage end-to-end recruitment for service related roles across Pharma/Biotech functions such as Data Science, Data Managers, Data Engineer, and other Support Services. The ideal candidate will have experience in pharma/life sciences recruitment and a passion for identifying top talent. Key Responsibilities: Handle full-cycle recruitment for positions in the pharmaceutical domain, including understanding role requirements, interviewing candidates, screening, scheduling interviews, and managing offers. Able to work in a fast paced environment with strict timelines Develop and maintain a pipeline of qualified candidates through proactive sourcing using job portals, social media, referrals, and databases. Collaborate with hiring managers and department heads to forecast hiring needs and create job descriptions. Coordinate and manage interview logistics and feedback collection. Maintain and update the applicant tracking system (ATS). Ensure compliance with recruitment and hiring policies, labor laws, and industry-specific regulations. Generate regular reports on recruitment metrics (e.g., time-to-fill, source of hire, quality of hire). Work with good colleges in hiring recent graduates. Qualifications and Skills: • Bachelor's degree in Human Resources, Life Sciences, or related field (MBA/PGDM in HR preferred). • 2-5years of recruitment experience, preferably in pharma, biotech, CRO, or healthcare sectors. • Excellent communication, negotiation, and interpersonal skills. • Proficiency in using MS Office tools. Preferred: Experience working with pharma clients or in a small startup serving pharma or technology industry. In office- Sector 132, Noida Bottom of Form

JD FOR CLINICAL DATA MANAGER Medtek Dot AI Pvt limited is a data science consulting company supporting global Pharma and Biotech companies. Our mission is to help Unlock insights and drive innovations using the data collected. We are a team of Biostatistician, Data Managers, Programmer s, Engineers and AI developers . Job Summary We are seeking an experienced and detail-oriented Clinical Data Manager (CDM) to oversee data management activities across clinical trials for pharmaceutical and biotech clients. The ideal candidate will ensure high-quality clinical data is collected, processed, and delivered in compliance with regulatory standards and timelines. Key Responsibilities Lead and manage end-to-end clinical data management activities for assigned projects. Develop and review data management plans (DMP), CRFs/eCRFs, edit checks, and database specifications. Coordinate with cross-functional teams including Biostatistics, Clinical Operations, Medical Writing, and Regulatory Affairs. Oversee database design, testing, and validation in EDC systems (e.g., Medidata Rave, Oracle InForm, or similar). Perform ongoing data review, discrepancy management, query generation and resolution. Ensure timely database lock, database freeze, and quality deliverables in accordance with project timelines. Monitor compliance with ICH-GCP, CDISC, FDA, EMA, and other regulatory guidelines. Act as primary point of contact for clients regarding data management activities. Reconcile Safety and Efficacy Data Qualifications Education & Experience: Bachelors or Masters degree in Life Sciences, Pharmacy, Health Informatics, or related field. 5-9 years of clinical data management experience in CRO, pharmaceutical, or biotech industry. Experience with EDC systems (e.g., Medidata Rave, Oracle InForm). Skills: Strong understanding of clinical trial processes and GCP. Knowledge of CDISC standards (SDTM), MedDRA. Excellent attention to detail and problem-solving skills. Strong communication, organizational, and project management skills. Ability to work independently and in a fast-paced, team-oriented environment. Preferred Qualifications Experience with oncology, rare disease, or other complex therapeutic areas. Familiarity with programming languages such as SAS or SQL is a plus. CDM certification (e.g., CCDM from SCDM) is an advantage. What We Offer Opportunity to work on cutting-edge clinical research projects. Collaborative, flexible, and growth-oriented work environment.

JD FOR R Programmer Title- Statistical Programmer/Sr. Statistical Programmer -R Programming We are seeking an experienced R Programmer to support Application development and statistical programming activities . The ideal candidate will have strong R programming skills with a solid understanding of clinical trial data, regulatory standards (e.g., CDISC, SDTM, ADaM), and open source libraries. Key Responsibilities: Develop and validate R programs to support CDISC dataset and statistical graph Create Markdown and Shiny appy for generating statistical tables and listings. Automate and streamline data wrangling, transformation, and visualization of clinical datasets using R and associated packages. Create and maintain Shiny apps, R Markdown reports, and automated pipelines for exploratory and statistical analyses. Collaborate with biostatisticians, data managers, and clinical teams to interpret clinical data and support study objectives. Contribute to statistical analysis plans (SAPs) and documentation for regulatory submissions (e.g., FDA, EMA). Ensure compliance with GxP, 21 CFR Part 11, and company SOPs in statistical programming deliverables. Required Qualifications: Bachelor's or Master's degree in Statistics, Biostatistics, Computer Science, Engineering or Quantitative field. 5+ years of experience in R programming within a clinical trials or pharmaceutical environment. Proficient in R packages such as tidyverse, haven, ggplot2, shiny, TEAL , knitr, and data.table. Knowledge of CDISC standards (SDTM, ADaM) and regulatory submission requirements. Experience with clinical data standards and regulatory documentation. Excellent attention to detail, problem-solving skills, and communication abilities. What We Offer: Opportunity to work on cutting-edge drug development programs. Career growth and access to global clinical research networks. Competitive salary and comprehensive benefits package.