scientific programmer

Eli Lilly

<div>At Lilly, we unite caring with discovery to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our employees around the world work to discover and bring life-changing medicines to those who need them, improve the understanding and management of disease, and give back to our communities through philanthropy and volunteerism. We give our best effort to our work, and we put people first. We&rsquo;re looking for people who are determined to make life better for people around the world.
Lilly Small Molecule Discovery is an organization purpose-built to create molecules that make life better for people. We focus on using cutting edge science to unlock new approaches that can treat people suffering from diseases with poor treatment options. We continually challenge ourselves to deliver molecules that can provide breakthrough efficacy with the highest possible safety margins. We are dedicated to optimizing our mindset, technology, and processes for faster, more nimble execution. Our success is built on a culture that empowers innovative problem solving through open collaboration and individual accountability.
Discovery Technology and Platforms is a newly established function within this organization. Its mission is to accelerate molecule discovery by building highly optimized foundational platforms, streamlining lab operations through advanced technologies and data connectivity, and intentionally investing in novel technologies and capabilities.
Data Foundry
Data Foundry is a multidisciplinary team dedicated to enabling and accelerating molecule discovery through scalable and reproducible data generation, fueled by advanced scientific programming, research informatics and automation solutions. The team also leads the design, implementation and validation of AI agent-compatible automation systems.
Position Summary: 
The Scientific Systems group within the Data Foundry is seeking a talented scientific programmer to join our dynamic team. This role bridges the gap between laboratory science and computational innovation, building fit-for-purpose data infrastructure and analytical pipelines that drive scientific discovery. This role will collaborate with foundational platforms and partner with Tech@Lilly and the Advanced Intelligence team (AI@Lilly) to ensure project data and software solutions are fully leveraged to facilitate scientific innovation and decision-making across the portfolio.
Key Responsibilities<ul><li>
Design, develop, and maintain data retrieval, cleaning, and processing pipelines for complex scientific datasets</li><li>
Collaborate with multidisciplinary teams to translate scientific requirements into technical solutions</li><li>
Implement scalable computational workflows for chemistry and biology research applications</li><li>
Develop and optimize software tools and automation scripts to enhance research productivity</li><li>
Ensure data integrity, quality control, and reproducibility across scientific computing systems</li><li>
Participate in agile development cycles with iterative improvement and rapid prototyping</li><li>
Document technical processes and provide training support to research teams</li></ul> 
Required Qualifications<ul><li>
BS/MS in Chemistry, Biology, Biochemistry, Computational Biology, Cheminformatics, Computer Science or related field with 5+ years scientific programming experience) with understanding of experimental data types and workflows</li><li>
Proficiency in multiple programming languages including Python, RESTful API, Java, C#, and SQL and Strong scientific prototyping/scripting</li><li>
Pharmaceutical and/or Biotech Research Industry Experience is required</li></ul>
Preferred Qualifications<ul><li>
Python Back-end or Web development experience is highly desirable</li><li>
Hands-on experience with popular cheminformatics systems such as RDKit, Schr&ouml;dinger Suite, or MOE (Molecular Operating Environment)</li><li>
Experience of integration of Benchling functions</li><li>
Experience with scientific data standards and ontologies</li><li>
Knowledge of cloud computing platforms (AWS, Azure, GCP)</li><li>
Familiarity with version control systems (Git) and CI/CD practices</li><li>
Experience with data visualization and analysis tools</li><li>
Background in machine learning or statistical modeling for scientific applications</li><li>
Experience with Linux environments and bash scripting</li><li>
Familiarity with agile methodologies and collaborative development practices</li><li>
Strong learning agility with willingness to adopt new technologies, languages, and tools to accomplish objectives</li><li>
Not afraid to step outside comfort zone and learn what's needed to get the job done</li><li>
Excellent interpersonal and communication skills, with a track record of effective scientist engagement</li></ul>
Lilly is dedicated to helping individuals with disabilities to actively engage in the workforce, ensuring equal opportunities when vying for positions. If you require accommodation to submit a resume for a position at Lilly, please complete the accommodation request form (https://careers.lilly.com/us/en/workplace-accommodation) for further assistance. Please note this is for individuals to request an accommodation as part of the application process and any other correspondence will not receive a response.
Lilly is proud to be an EEO Employer and does not discriminate on the basis of age, race, color, religion, gender identity, sex, gender expression, sexual orientation, genetic information, ancestry, national origin, protected veteran status, disability, or any other legally protected status. 
Our employee resource groups (ERGs) offer strong support networks for their members and are open to all employees. Our current groups include: Africa, Middle East, Central Asia Network, Black Employees at Lilly, Chinese Culture Network, Japanese International Leadership Network (JILN), Lilly India Network, Organization of Latinx at Lilly (OLA), PRIDE (LGBTQ+ Allies), Veterans Leadership Network (VLN), Women&rsquo;s Initiative for Leading at Lilly (WILL), enAble (for people with disabilities). Learn more about all of our groups.
Actual compensation will depend on a candidate&rsquo;s education, experience, skills, and geographic location. The anticipated wage for this position is
$87,000 - $193,600
Full-time equivalent employees also will be eligible for a company bonus (depending, in part, on company and individual performance). In addition, Lilly offers a comprehensive benefit program to eligible employees, including eligibility to participate in a company-sponsored 401(k); pension; vacation benefits; eligibility for medical, dental, vision and prescription drug benefits; flexible benefits (e.g., healthcare and/or dependent day care flexible spending accounts); life insurance and death benefits; certain time off and leave of absence benefits; and well-being benefits (e.g., employee assistance program, fitness benefits, and employee clubs and activities).Lilly reserves the right to amend, modify, or terminate its compensation and benefit programs in its sole discretion and Lilly&rsquo;s compensation practices and guidelines will apply regarding the details of any promotion or transfer of Lilly employees.
#WeAreLilly</div>

Principal Scientist - Data Foundry Scientific Developer

Merck

<div>Job Description
In BARDS (Biostatistics and Research Decision Sciences), a distinguished department within our company's renowned Research and Development division, quantitative scientists, in partnership with other subject matter experts, apply state-of-the art scientific methodologies and tools to enable the discovery, development, regulatory approval, manufacturing, and marketing of medical drugs and vaccines for the benefit of patients and global human health.
This position provides high quality statistical programming analysis and reporting deliverables for global stakeholders in Early Development Statistics and global PK/PD modeling and simulation stakeholders spanning all our company therapeutic areas except early oncology.
The Associate Principal Programmer will gather and interpret user requirements for analysis and programming requests in close collaboration with stakeholders (statisticians/modelers) and clinical colleagues, retrieve the required data, transform the data into analysis/modeling datasets, and develop tables and figures according to statistical/modeling analysis plan.
The Associate Principal Programmer will partner with stakeholders to solve problems; reduce the amount of programming task being completed by stakeholders to facilitate an increase in efficiency and compliance for statistical/modeling analyses. The Associate Principal Programmer will write programs to analyze data with statistical methods which are not currently available through commercial software packages. The Associate Principal Programmer will be a key collaborator with statisticians, modelers, and colleagues in other related function areas. 
Primary Activities:<ul><li>
Pre-process, filter, and manipulate complex data for the analyses of molecular biomarker data, imaging data, and external data other than traditional laboratory data</li><li>
Provide technical consultation and analytical support to early development statisticians for exploratory and unplanned statistical analyses</li><li>
Prepare compliant programming code for regulatory submissions including analysis/modeling datasets, tables, listings, figures and associated documentation</li><li>
Ensure programmatic traceability from data source to analysis/modeling result</li><li>
Maintain and manage a project plan including resource forecasting</li><li>
Support the development of programming standards to enable efficient and high-quality production of programming deliverables</li><li>
Represent statistical programming on process improvement activities</li></ul>
Education and Minimum Requirement:
BA/BS in Computer Science, Statistics, Applied Mathematics, Life Sciences, Engineering or related field plus 9 years SAS programming experience in a clinical trial environment 
MS in Computer Science, Statistics, Applied Mathematics, Life Sciences, Engineering or related field plus 7 or more years SAS programming experience in a clinical trial environment 
Department Required Skills and Experience:<ul><li>
Excellent interpersonal skills and ability to negotiate and collaborate effectively</li><li>
Excellent written, oral, and presentation skills</li><li>
Broad knowledge and significant experience in developing analysis and reporting deliverables for R&amp;D projects (data, analyses, tables, graphics, listings)</li><li>
Strong project management skills; leadership at a program level; determines approach and ensures consistency and directs development of others when opportunities arise; ability to engage key stakeholders</li></ul>
Position Specific Required Skills and Experience:<ul><li>
Significant expertise in SAS and clinical trial programming including data steps, procedures, SAS/MACRO, SAS/GRAPH</li><li>
Designs and develops complex programming algorithms</li><li>
Ability to comprehend analysis plans which may describe methodology to be programmed; understanding of statistical terminology and concepts; Implements statistical methods not currently available through commercial software packages.</li><li>
Experience in CDISC SDTM and ADaM standards</li><li>
Demonstrated success in the assurance of deliverable quality and process compliance</li><li>
Thrives in an exploratory environment, handling non-standard data in a variety of formats with minimal requirements; knowledge of pharmaceutical development processes</li><li>
Efficiently manipulates very large databases including complex data preprocessing, filtering, and manipulation</li><li>
Programming expertise with clinical endpoint data (efficacy and safety) and pharmacokinetic data (raw concentration data, derived PK parameters)</li><li>
Strategic thinking - ability to turn strategy into tactical activities; design of statistical databases with the end in mind that optimize analysis and reporting and leverage departmental standards and industry best-practices</li></ul>
Preferred Skills and Experience:<ul><li>
Familiarity with clinical pharmacology concepts and pharmacokinetics concepts</li><li>
Experience with at least one other software than SAS (e.g., R, Splus, NonMem)</li><li>
Good working knowledge of reporting processes (SOPs) and software development life-cycle (SDLC)</li><li>
Utilizes and contributes to the development of standard departmental SAS macros</li><li>
Ability and interest to work across cultures and geographies</li><li>
Ability to complete statistical programming deliverables through the use of global outsource partner programming staff</li><li>
Experience providing technical and/or programming guidance and mentoring to colleagues</li><li>
Experience in process improvement</li><li>
Active in professional societies</li></ul>
BARDS2020
eligibleforERP
SPjobs
VETJOBS
EBRG
Required Skills:
Clinical Trials, Data Modeling, Leadership, Numerical Analysis, Pharmaceutical Development, Pharmacokinetics, PKPD Modeling, Project Resource Management, Python (Programming Language), R Programming, SAS Graphs, Stakeholder Relationship Management, Statistical Programming, Waterfall Model
Preferred Skills: 
US 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 Rights
EEOC 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&rsquo;s thinking and approach problems collectively.
Learn more about your rights, including under California, Colorado and other US State Acts
U.S. Hybrid Work Model
Effective September 5, 2023, employees in office-based positions in the U.S. will be working a Hybrid work consisting of three total days on-site per week, Monday - Thursday, although the specific days may vary by site or organization, with Friday designated as a remote-working day, unless business critical tasks require an on-site presence.This Hybrid work model does not apply to, and daily in-person attendance is required for, field-based positions; facility-based, manufacturing-based, or research-based positions where the work to be performed is located at a Company site; positions covered by a collective-bargaining agreement (unless the agreement provides for hybrid work); or any other position for which the Company has determined the job requirements cannot be reasonably met working remotely. Please note, this Hybrid work model guidance also does not apply to roles that have been designated as &ldquo;remote&rdquo;.
The salary range for this role is
$139,600.00 - $219,700.00
This 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&rsquo;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 Ordinance
Los 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&rsquo; Fair Chance Initiative for Hiring Ordinance
Search Firm Representatives Please Read Carefully 
Merck &amp; Co., Inc., Rahway, NJ, USA, also known as Merck Sharp &amp; 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:
Domestic
VISA Sponsorship:
Yes
Travel Requirements:
10%
Flexible Work Arrangements:
Hybrid
Shift:
Not Indicated
Valid Driving License:
No
Hazardous Material(s):
N/A
Job Posting End Date:
12/5/2025<ul><li>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. 
</li></ul> 
Requisition ID:R369521</div>

Associate Principal Statistical Programmer, Early Stage Development and Pharmacokinetic/Pharmacodynamic Modeling and Simulation- Hybrid

SATYAM VENTURE ENGINEERING SERVICES

<div>Job Title:
<ul><li>MBSE Matlab/mScripting Requirement</li>
<li>Experience:</li>
<li><ul><li>4 - 5 Years</li>
<li><ul>
</ul></li><li>Qualification:</li>
<li><ul><li>B.E/B.Tech or M.E/M.Tech (ECE, Mechatronics)</li>
</ul></li>
<li>Job Location:</li>
<li><ul><li>Chennai</li>
</ul></li>
<li>Job Description:</li>
<li><ul>
<li>Thoroughly analyze existing MATLAB codebase, algorithms, data structures, and functionalities to gain a comprehensive understanding of their purpose, implementation details, and underlying mathematical/scientific principles.</li>
<li>Document the intricacies of the MATLAB tools, identifying core logic, dependencies, and potential challenges for migration.</li>
<li>Collaborate with end-users and domain experts of the current MATLAB tools to capture implicit requirements, usage patterns, and critical performance characteristics.</li>
<li>Develop detailed migration plans, including phased approaches, risk assessments, and resource estimates for converting MATLAB components to Python.</li>
<li>Design the architecture and data flow for the new Python-based tools, ensuring scalability, maintainability, and alignment with overall software engineering standards.</li>
<li>Select appropriate Python libraries, frameworks, and methodologies for optimal translation of MATLAB functionalities (e.g., NumPy for matrix operations, SciPy for scientific functions, Pandas for data handling).</li>
<li>Translate complex MATLAB algorithms and numerical methods into efficient, well-structured, and idiomatic Python code.</li>
<li>Implement new features or enhancements as identified during the migration process, leveraging Python's ecosystem.</li>
<li>Develop robust data processing pipelines and interfaces to integrate with existing or new data sources.</li>
<li>Design and implement comprehensive test suites (unit, integration, regression tests) to ensure functional correctness and numerical fidelity of the Python tools against their MATLAB counterparts.</li>
<li>Perform rigorous validation of results, comparing outputs from MATLAB and Python implementations to ensure accuracy and consistency.</li>
<li>Identify and resolve performance bottlenecks in the Python code, optimizing algorithms and data structures for efficiency.</li>
<li>Utilize profiling tools to benchmark and improve the execution speed of critical components.</li>
<li>Create clear, concise, and comprehensive technical documentation for the new Python tools, including design specifications, API documentation, user guides, and migration reports.</li>
<li>Provide training and mentorship to other team members on the new Python codebase and best practices for scientific computing in Python.</li>
<li>Contribute to establishing coding standards and best practices for scientific Python development within the team.</li>
<li>Work closely with cross-functional teams (e.g., software engineers, data scientists, domain experts) to ensure seamless integration of the migrated tools into existing systems and workflows.</li>
<li>Participate in code reviews, architectural discussions, and agile development ceremonies.</li>
<li>Manage version control (Git) for the Python codebase, ensuring proper branching, merging, and release management.</li>
</ul></li>
<li>Skill set:</li>
<li><ul>
<li>MATLAB scripting, Python</li>
</ul></li>
<li>Domain Knowledge:</li>
<li><ul>
<li>Expert-level knowledge of Python syntax, object-oriented programming, and common design patterns.</li>
<li>Deep understanding and hands-on experience with core scientific Python libraries:</li>
<li>NumPy, SciPy, Pandas,</li>
<li>Matplotlib, Seaborn, Plotly/Bokeh: For data visualization and graphical output replication.</li>
<li>Familiarity with other relevant libraries</li>
<li>Ability to read, understand, and debug complex MATLAB code, including knowledge of MATLAB's specific data types, functions, and programming paradigms.</li>
<li>Experience with MATLAB's toolboxes relevant to the existing tools</li>
<li>Understanding of MATLAB's plotting capabilities and GUI development</li>
<li>Solid understanding of common numerical algorithms, linear algebra, differential equations, optimization techniques, and statistical methods.</li>
<li>Ability to identify and address potential numerical precision issues during migration.</li>
<li>Proficiency with Git for version control.</li>
<li>Experience with unit testing (e.g., pytest) and integration testing frameworks.</li>
<li>Knowledge of code quality tools (linters like Flake8, Black) and static analysis.</li>
<li>Understanding of software design principles (SOLID, DRY).</li>
<li>Experience with various data formats (e.g., HDF5, CSV, Parquet, JSON, XML).</li></ul></li></ul></li></ul></div>

MBSE Matlab/mScripting Requirement - ZR_1961_JOB

AstraZeneca

<div>Job Title: Senior Data Programmer CPQP Programming
Global Career Level: D
Skillsets Required: PKPD / Pharmacometrics / NONMEM / SAS Programmer
Introduction to role:
Are you interested in shaping the future of drug development? We are looking for a Senior Data Programmer CPQP Programming to join our Clinical Pharmacology and Quantitative Pharmacology Data Programming team. In this position, you will be responsible for preparing, programming, validating, and diagnosing data to support Pharmacometrics and Clinical Pharmacology analyses. Your work will span all phases of drug development at both the study and compound levels.
Accountabilities: 
As a Senior Data Programmer CPQP Programming, you will be responsible for data cleaning, manipulation, transformation, and integration at both the study and compound level. You will apply advanced data integration techniques that directly contribute to the value of each study and compound. Key responsibilities include pooling data from study and compound-level SDTM/ADaM datasets to prepare analysis-ready data for Pharmacometrics Modeling and Simulation (M&amp;S) software, such as NONMEM. This work will play a critical role in informing study design, dose selection, dose justification and guiding go/no-go decisions. Additionally, you will contribute to internal initiatives that advance the Pharmacometrics discipline and ensure compliance with Good Clinical Practice (GCP) regulations.
Essential Skills/Experience:<ul><li>
Proficient oral and written English communication skills</li><li>
Strong SAS/R programming skills</li><li>
Bachelor&rsquo;s degree MS preferred with 6 to 8 years relevant experience required</li><li>
Expert knowledge of data preparation and programming practices (CDISC, SDTM, ADaM)</li><li>
Demonstrated data programming and clinical development expertise</li><li>
Good knowledge of global regulatory, compliance, processes, standards</li><li>
Varied programming languages (SAS, R, Python)</li><li>
Experience in early and late-stage drug development</li><li>
Quantitative/Scientific background (Statistics, Engineering, Biological Science)</li></ul>
Desirable Skills/Experience:<ul><li>
Demonstrated expertise in data preparation and programming to support Pharmacometrics Modeling and Simulation (M&amp;S) software (e.g. NONMEM, Monolix, R, Matlab)</li><li>
Knowledge in pharmacology, drug targets and core Therapy areas (e.g. Oncology, Respiratory, Renal Metabolism etc.)</li><li>
Relevant regulatory experience</li></ul>
When we put unexpected teams in the same room, we unleash bold thinking with the power to inspire life-changing medicines. In-person working gives us the platform we need to connect, work at pace and challenge perceptions. That's why we work, on average, a minimum of three days per week from the office. But that doesn't mean we're not flexible. We balance the expectation of being in the office while respecting individual flexibility. Join us in our unique and ambitious world.
At AstraZeneca, we are committed to making a difference by fusing data and technology with scientific innovation to achieve breakthroughs in healthcare. Our dynamic environment encourages creativity and bold decision-making as we strive to treat, prevent, modify, and even cure complex diseases. With a focus on collaboration and inclusivity, we unite diverse global knowledge to create impactful solutions for patients worldwide. Here, curiosity thrives as we explore new ways to handle diseases and push the boundaries of science.
Ready to make an impact? Apply now and be part of a team that is transforming the future of healthcare!</div>

Senior Data Programmer CPQP Programming (PKPD / Pharmacometrics / NONMEM / SAS Programmer)

NSF International

<div>Plan, assign and oversee all the statistical programming activities clinical trials/studies and manage resources; Build datasets from clinical database to perform statistical analysis and data visualization of biological data; Revise and develop standard operating procedures to ensure compliance with Good Clinical Practices; Provide expertise in development and quality control process for scientific programming; Develop processes for process improvement and automation; Create and maintain programming specification documents; Perform edit checks and assist review edit specifications; Utilize SDTM/ADaM guidelines to prepare SAS programs for standardized clinical datasets; Validate the programmed analysis clinical datasets, tables, listing and figures; Represent department in internal cross-functional project team meetings and audits; Participate in department and cross functional technology development and process improvement initiatives; Assist in compiling technical documents for internal and external audits; Work in tandem with Biostatistics and Data Management members on various clinical projects; and Provide training and assistance to junior members of the Scientific Programming group.
Location: 20201 Century Blvd, Suite 450, Germantown, Maryland 20874 
 
Education: Bachelor&rsquo;s &ndash; Bioinformatics, Pharmaceutical Science or a related field of study; Will accept equivalent of foreign degree.
Experience: None.
Education and/ or Experience must include:
<div><ul><li>Instrumental Methods of Analysis;
</li></ul><ul><li>Research Methodology and Statistical Methods;
</li></ul><ul><li>Chromatographic Methods of Analysis; and
</li></ul></div>Biological Methods of Screening
Sheri Threadgill
Principal Human Resources Business Partner
Amarex Clinical Research, LLC.
20201 Century Blvd., Ste. 450
Germantown, Maryland 20874
Attn: LC25-101</div>
 <div></div>
 <div></div>
 <div>About Us: With a legacy spanning more than 80 years, NSF leverages science and innovation to improve human and planet health. We provide science-driven, independent testing, inspection, certification, and advisory services and develop the very standards that drive the food, water, and life sciences industries worldwide. We empower our clients to navigate shifting regulations to improve consumer health, safety, and quality of life.
One of our core values is We Are One NSF. This means that while we&rsquo;re one team, we embrace the cultural, ethnic, language, and demographic diversity that reflects the societies in which we live and work.
Come join a team that makes a difference in the world. More information about NSF can be found at nsf.org.
NSF is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to, among other things, race, color, religion, sex, sexual orientation, gender identity, national origin, age, status as a protected veteran, or disability.
Notice to Agency and Search Firm Representatives: Please note that NSF is not accepting unsolicited resumes from agencies/search firms for this role. Resumes submitted to an NSF employee by a third-party agency without a valid written &amp; signed search agreement between NSF and said third-party agency will become the sole property of NSF. No fee will be paid if a candidate is hired as a result of an unsolicited agency or search firm referral. Thank you.</div>
 About the Team: From research to patient, NSF's expert team provides comprehensive regulatory, quality and clinical support to pharmaceutical, biotech, medical devices, in-vitro diagnostics, and combination products clients across the product life cycle to navigate complex regulations and industry challenges.

Director, Scientific Programming

Medpace

<div>Job Summary :
<div>
Our global activities are growing rapidly, and we are currently seeking a full-time, office-based Clinical Database Designer to join our Biometrics team. This position will work in a team to accomplish tasks and projects that are instrumental to the company&rsquo;s success. If you want an exciting career where you use your previous expertise and can develop and grow your career even further, then this is the opportunity for you.</div>
Responsibilities :
<ul><li>Maintain eCRF and Edit Check Specification standard templates according to CDISC standards for data collection and data submission;</li><li>
Develop and maintain eCRF specifications on a study-by-study basis (e.g., reviewing protocol and customize library eCRFs to apply for the study) from database build through database lock (including Change Requests);</li><li>
Develop and maintain Edit Check Specifications from database build through database lock (including Change Requests) to ensure that all data collected are present, logical, and per expected protocol assessment schedule and completion guidelines;</li><li>
Perform validation of both the eCRF and the edits per the specifications ensuring that all possible entry scenarios are tested and documented. Accountable for providing reliable and concise feedback to clinical data programmer;</li><li>
Liaise and educate the Data Manager and Sponsor to ensure that eCRFs are well understood, and the EDC database is set up per Sponsor expectations (e.g., attend ongoing meetings with the Sponsor during setup of study);</li><li>
Liaise with Clinical Db Programmer to ensure that eCRF and Edit Check Specifications are clearly defined and can be accomplished in the referenced system;</li><li>
Design and develop customized project-level reports that are useful to the team via the reporting tools within the EDC systems (e.g., Business Objects, JReview);</li><li>
Lead eCRF specification review meetings with internal project team to discuss eCRF specifications; and</li><li>
Lead eCRF specification review meetings with external project team to discuss eCRF specifications and speak knowledgeably about decisions made and technical design options if Sponsor does not agree with current design.</li></ul>
Qualifications :
<ul><li>Bachelor&rsquo;s degree/Advanced degree in Life Sciences or Computer Science or equivalent;</li><li>
At least one year experience building specifications and/or performing UAT for EDC databases</li><li>
Excellent verbal and written communication skills; and</li><li>
Meticulous attention to detail.</li></ul>
Medpace Overview :
<div>
Medpace is a full-service clinical contract research organization (CRO). We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through its scientific and disciplined approach. We leverage local regulatory and therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, employing more than 5,000 people across 40+ countries.</div>
Why Medpace? :
<div>
People. Purpose. Passion. Make a Difference Tomorrow. Join Us Today.</div><div></div><div> 
The work we&rsquo;ve done over the past 30+ years has positively impacted the lives of countless patients and families who face hundreds of diseases across all key therapeutic areas. The work we do today will improve the lives of people living with illness and disease in the future.</div><div></div> 
Medpace Perks<ul><li>
Flexible work environment</li><li>
Competitive compensation and benefits package</li><li>
Competitive PTO packages</li><li>
Structured career paths with opportunities for professional growth</li><li>
Company-sponsored employee appreciation events
</li><li>Employee health and wellness initiatives</li></ul><div>
Awards</div><ul><li>
Recognized by Forbes as one of America's Most Successful Midsize Companies in 2021, 2022, 2023 and 2024</li><li>
Continually recognized with CRO Leadership Awards from Life Science Leader magazine based on expertise, quality, capabilities, reliability, and compatibility</li></ul><div></div><div> 
What to Expect Next</div><div>
A Medpace team member will review your qualifications and, if interested, you will be contacted with details for next steps.</div></div>

Clinical Database Designer (Mumbai)

Foxconn Industrial Internet - FII

<div>Job Summary:
This role designs, develops, documents, tests, implements, and debugs new and existing software solutions for large-scale proprietary software for internal use. Serves as a technical expert on development projects. Participates in the full development life cycle, including requirements analysis and design. Writes technical specifications based on conceptual design and stated business requirements. Supports, maintains, and documents software functionality. Identifies and evaluates new technologies for implementation. Analyzes components to find causes of errors and revise programs as needed. Analyzes user needs, system requirements and business processes to determine technical requirements. Consults with end user to prototype, refine, test, and debug components to meet needs.
Responsibilities:<ul><li>
10%, Analyzes user needs, system requirements, and business processes</li><li>
25%, Maintain the source code for existing software products, participate in code reviews, software design and development process</li><li>
25%, Develop customized applications for company internal use</li><li>
15%, Identify and debug source cause of issues</li><li>
15%, Provide issue resolution through configuration or code changes</li><li>
10%, Perform or support product installations, upgrades and updates</li></ul>
Skills/Qualifications:<ul><li>
Python (3.6 and higher) programmer candidates, 1 - 3 years of development experience</li><li>
VueJS 2+ Framework programmer candidates, 1-2 year of development experience</li><li>
 Intermediate knowledge and experience using Front-End Layout such as JQuery, Ajax, CSS</li><li>
Django Framework 4.1 programmer candidates at least 1 year of development experience</li><li>
RESTful API&rsquo;s programmer candidates, at least 1 year of development experience</li><li>
Database development using Oracle, SQL Server 2019 and higher, PostgreSQL 11+</li><li>
Advanced knowledge and experience with Linux (CentOS, RedHat, Ubuntu) and Windows Server (2019 and higher). Including: IIS, PowerShell, Command Prompt and batch file scripting (desired not required)</li><li>
Excellent communication, organization, and interpersonal skills</li><li>
Excellent problem-solving skills with extreme attention to detail</li><li>
Outstanding work ethic and commitment to individual and organizational success</li><li>
Excellent analytical and advanced troubleshooting skills with end-users/clients</li><li>
Ability to manage multiple tasks and projects, both independently and as part of a team</li><li>
Demonstrated ability to learn new things and continuously drive process improvement.</li></ul>
Plus/Desired:<ul><li>
Experience with Git Repositories (GITLAB) or JIRA</li><li>
Containerization using Docker.</li><li>
K8S</li><li>
SQL Reporting Services</li></ul>
Educational Requirements:<ul><li>
Bachelor degree in a business or IT-related area, IT Security-related classes a plus, BS in Computer Science a plus.</li><li>
Any software programming certifications are a plus.</li></ul>
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Software Engineer (Automation)

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