Senior Clinical System Designer Job at iconplc (Bangalore)

Senior Prompt Designer – AI Clinical Products

As a Senior Prompt Designer, you will play a defining role in shaping the qualit...

Location

Canada , Montréal

Salary:

Not provided

DesignX Community

Expiration Date

Until further notice

Requirements

5+ years of professional experience in AI/ML, product development, computational linguistics, or a closely related field
2+ years of hands-on prompt "engineering" experience in production LLM systems, ideally in a B2B SaaS or regulated industry context
Demonstrable experience decomposing complex prompts into modular, chained architectures
Experience designing or significantly improving LLM evaluation frameworks
Strong familiarity with frontier commercial LLM APIs
Experience working within or alongside healthcare, clinical, or life sciences domains is a strong asset
Proficiency in Python or another scripting language for building eval pipelines or prompt tooling is an asset
Experience with self-hosted or open-weight models is an asset
Advanced proficiency in English, both written and spoken
French is an asset

Job Responsibility

Audit and re-architect CoeurWay's existing monolithic prompts into a modular chain of focused, maintainable prompts
Lead the selection, evaluation, and pairing of language models to specific prompt tasks
Own the quality of AI-generated clinical outputs
Evolve and re-align our existing evaluation framework
Establish and maintain a systematic approach to output validation
Design and implement new prompts and evaluation suites to support new features
Collaborate with the GenAIOps to ensure prompts are production-ready
Develop a deep understanding of clinical workflows and the needs of healthcare providers
Stay current on the rapidly evolving LLM landscape
Contribute to internal documentation, standards, and best practices for prompt "engineering"

What we offer

Remote work and flexibility
RRSP contribution
Healthcare insurance from day one
Paid time off: 3 weeks + 1 additional week between Christmas and New Year
Annual training allowance ($1,500)
An onboarding program
All IT equipment is provided
Internal growth opportunities
Support from a wellness and social committee
A company culture focused on transparency, collaboration, and innovation

Fulltime

Senior Clinical Data Analyst

Parexel is currently seeking a Senior Clinical Data Analyst to join us in either...

Location

United Kingdom; Poland; South Africa , Remote

Salary:

Not provided

Parexel

Expiration Date

Until further notice

Requirements

Bachelor's Degree required, preferably in the scientific/healthcare field
Proven leadership experience
Good project management skills and a proven ability to multitask
At least five years' or preferably up to 8 years' experience, in Data Management for the pharmaceutical/biotechnology industry
Understanding of the scope and focus of Phase I – IV clinical studies, and a proven ability to perform some of the core Data Management tasks and interact with vendors
A high level of Phase I experience is essential
A comprehensive understanding of regulatory guidelines and industry standards (e.g., ICH/FDA guidance, CDISC standards, GCDMP, 21 CFR 11, MedDRA, WHO Drug Dictionaries, etc.) and their application to Data Management practice
Attention to detail and the ability to work individually, within a multi-disciplinary team, as well as with external partners and vendors
Strong English language written and verbal communication skills
Able to travel to meetings or training seminars on occasion

Job Responsibility

Lead a large clinical study or a series of related studies with minimum guidance
Represents Data Management on the CTWG for assigned studies
Provide mentoring and training to lower-level Data Management staff assigned to your studies
Manage and monitor the progress of data management activities with CROs or other vendors on assigned studies
build effective relationships with CRO / vendor counterparts
Review protocols for appropriate data capture including electronic Case Report Form (eCRF) design
Be able to perform a thoroughly detailed review of eCRF data requirements
Interact with CRAs, programmers, study managers and statisticians in designing eCRFs and creating the annotated eCRF and CRF completion guidelines
Lead the development of data edit check specifications and data listings
Coordinate the design and testing of Electronic Data Capture (EDC) systems according to company standards

What we offer

annual performance-based bonus plan
annual salary review
total rewards incentives

Fulltime

Senior Clinical Informaticist

The Senior Clinical Informaticist is a key leader in bridging clinical workflows...

Location

United States , Jacksonville

Salary:

Not provided

Baptist Health (Florida)

Expiration Date

Until further notice

Requirements

Assisting with development, optimization, integration, and providing support for electronic medical records and various information systems to support patient care within the organization
Analyzing processes and the collection of data to streamline workflow and integrate information technologies within the clinical practice for a variety of healthcare roles
Utilizing methods of information retrieval and presentation to improve patient safety
Incorporating evidenced based/best practice standards of care in the design and optimization of systems
Working alongside a variety of healthcare roles including nurses and physicians to support and train on healthcare technology systems
Requires in-depth conceptual and practical knowledge of informatics and basic knowledge of related job disciplines
Solving complex problems utilizing critical thinking skills with minimal guidance
Exhibiting excellent communication and consensus-building skills
Inpatient nursing
Bachelor of Science

Job Responsibility

Optimizing the intersection of clinical practice and information technology
Leveraging clinical expertise and advanced informatics knowledge to improve patient care, support clinical workflows, and facilitate the effective use of electronic health records (EHR) and other health information systems
Acting as a liaison between clinical staff, IT professionals, and other stakeholders, ensuring that technology solutions align with organizational goals and regulatory requirements
Design, implementation, and support of clinical information systems
Collaborating with healthcare teams to analyze and improve clinical processes
Training staff on system use
Providing ongoing support for electronic health records (EHR) and other clinical applications

Fulltime

Senior System Analyst

To provide technical support for assigned applications.

Location

United States , Liberty

Salary:

Not provided

The University of Kansas Health System

Expiration Date

Until further notice

Requirements

Bachelors Degree Information Technology, Business Admin or related field
OR equivalent combination of education and experience.
5 or more years healthcare IT experience.
5 or more years extensive experience in providing technical support and maintenance in assigned product.

Job Responsibility

Perform technical application configuration and configure/run reports at user request
Codes, tests, debugs, implements, and documents programs or technical configuration
Interact with Business and Clinical representatives during the software build or configuration and test process
Communications effectively with all parties related to assigned process are and internal management
Identify and escalate critical issues in a timely manner
Participate in focus groups, workshops, committee meetings, and attend vendor training and demonstrations
Establish a consistent communication strategy with outside vendors/agencies and defines the associated deliverables
Work with Clinical and/or Business Analyst to understand the end user’s product specific requirements and configuration and translate them to technical design specifications and data flow from which programs are developed and coded
Must be able to perform the professional, clinical and or technical competencies of the assigned unit or department.

Fulltime

Senior Clinical Data Scientist - Applied Intelligence Solutions

We are seeking a Senior Clinical Data Scientist to join the Catalysts team, focu...

Location

United States , Seattle

Salary:

155000.00 - 170000.00 USD / Year

Truveta

Expiration Date

Until further notice

Requirements

Bachelor’s degree or equivalent experience in a quantitative or technical field such as computer science, data science, statistics, engineering, or a related discipline
Strong understanding of how large language models consume, retrieve, and reason over knowledge, and how to structure information so it can be used efficiently and reliably by intelligence systems
Solid understanding of healthcare problem spaces such as clinical research, HEOR, clinical trials, and healthcare operations, and the types of questions and decisions users need support with
Hands on experience using generative AI tools to synthesize, generate, and refine knowledge assets including guidance, templates, prompts, and structured explanations
Ability to design and prototype applied intelligence solutions for specific problem types by combining domain knowledge, templates, prompts, guardrails, and workflows
Comfortable writing and reviewing production quality analysis code (e.g., SQL, Python, or R) to prototype analyses, validate logic, and create reusable examples that intelligence and teammates can reuse
Create clear, reusable intelligence assets by synthesizing expert input or authoring directly, translate technical and domain specific concepts into guidance that is understandable and actionable for a wide range of audiences, and explicitly define exclusions and limitations where intelligence should not provide answers

Job Responsibility

Independently build small scale, concrete intelligence solutions for specific healthcare problems by creating the required knowledge assets, examples, reference analyses, and guardrails that allow intelligence to answer the right questions and respect clear boundaries, within current platform capabilities
Break down healthcare problems in areas such as clinical research, HEOR, and clinical trials into the concrete assumptions, decision points, and data considerations that intelligence needs to handle correctly
Create and maintain the domain knowledge, guidelines, templates, and decision logic that intelligence systems need in order to perform effectively in each problem domain
Shape how intelligence agents operate at a practical level by defining task breakdowns, decision logic, and required knowledge, working within current platform constraints
Work with domain experts and users to extract assumptions, heuristics, and expertise, and convert them into structured inputs that intelligence systems can reliably consume
Apply an understanding of how generative AI systems retrieve and reason over knowledge to improve correctness, safety, and consistency of intelligence outputs, using concrete examples and test questions
Define and validate constraints, exclusions, and limitations to ensure intelligence outputs are appropriate, trustworthy, and aligned with real world healthcare use
Work closely with colleagues across the Catalysts team, contributing domain expertise, intelligence design, and reusable assets into a shared knowledge base, and collaborating as peers on intelligence solutions rather than owning a separate execution pipeline

What we offer

Interesting and meaningful work for every career stage
Comprehensive benefits with strong medical, dental and vision insurance plans
401K plan
Professional development & training opportunities for continuous learning
Work/life autonomy via flexible work hours and flexible paid time off
Generous parental leave
Regular team activities (virtual and in-person)
Additional compensation such as incentive pay and stock options for certain roles

Fulltime

Senior Clinical Database Programmer

The Senior Clinical Database Programmer is responsible for the programming of hi...

Location

India , Remote

Salary:

Not provided

Parexel

Expiration Date

Until further notice

Requirements

Bachelor's degree in Life Science, Computer Science or equivalent
Minimum of 5 years of relevant experience in a pharmaceutical, biotech, CRO, or Regulatory Agency with an emphasis on building data collection and assimilation solutions
Technical skills and experience using relational databases (e.g. Oracle InForm, Rave EDC System, Oracle DMW, MS SQL Server or MS Access)
Experience in Oracle, PL/SQL, SAS, Java, relational database design and database programming skills
Rave Custom Function Programming skills are mandatory
Strong communication (written and oral), decision-making, influencing, negotiation, and project management skills
Proficiency in the use of Microsoft Office Suite of tools (Outlook, Word, Excel, etc.)
Understanding of drug development process and data operations required for the reporting of clinical trial data (e.g. data review, study reports, regulatory submissions, safety updates, etc.)
Understanding regulatory requirements and relevant data standards
CDISC knowledge and experience are preferable

Job Responsibility

Works closely with department roles and cross-functional study team members to create data capture solutions that support the quality and timely delivery of data required per standard and study specific data review plans
Complies with applicable SOPs and work practices
Serves as subject matter expert in one or more technologies
Leads and contributes to cross-functional technical initiatives in collaboration with clients Digital and other teams
Supports knowledge development of data capture tools and methods that support the accuracy and integrity of study data

Senior Clinical Trial Manager

The Sr. Clinical Trial Manager (CTM) is responsible for supporting or leading th...

Location

United States , Madison

Salary:

91000.00 - 155000.00 USD / Year

Exact Sciences

Expiration Date

Until further notice

Requirements

Bachelor’s degree in the life sciences or field as outlined in the essential duties
5+ years of experience in clinical research
1+ year of experience of experience leading project teams through the start-up, study conduct, data management, analysis, close out and report writing of clinical studies
Clinical monitoring experience including data review, query resolution, protocol deviation identification/tracking/trending, site initiation, site maintenance, and site closeout visits
Experience writing, reviewing and editing protocols
Knowledge of applicable quality standards (e.g. Good Clinical Practices (ICH/GCP), ISO 20916) and applicable local and national regulations governing clinical research
Applicants must be currently authorized to work in country where work will be performed on a full or part-time basis
Demonstrated ability to perform the Essential Duties of the position with or without accommodation
Experience providing oversight to external vendors (e.g. CRO, central labs, call centers, DCT providers)

Job Responsibility

Coordinate and oversee the operational aspects of a study including planning, start-up, enrollment and close out activities
Prepare, review and implement study related plans and documents including project timelines, study protocols, informed consent forms (ICFs), recruitment plans, monitoring plans, study budgets, site contracts & budgets, vendor management plans and other essential clinical study documents
Develop plans for systems and materials required to support the efficient execution of clinical studies
Develop, implement and maintain tools to manage, monitor and report on study health & operations, project timelines, and study finances
Participate in study database development by reviewing and contributing to case report form (CRF) design, CRF completion guideline development, edit check & manual data review requirements, and participation in user acceptance testing (UAT)
Oversee sample management activities including planning, sample handling, kit supply management, sample shipping, processing, and resulting
Develop site recruitment plans and is responsible for the identification, selection, start-up and performance monitoring of clinical research sites
Develop study budgets and is responsible for accurately forecasting and managing study expenses
Oversee site contracting and study budget management
Oversee study and site management activities such as, training, data entry & query resolution, TMF maintenance

What we offer

Paid time off (including days for vacation, holidays, volunteering, and personal time)
Paid leave for parents and caregivers
A retirement savings plan
Wellness support
Health benefits including medical, prescription drug, dental, and vision coverage
Bonus eligibility

Fulltime

Senior Clinical Supplies Project Manager

ICON plc is a world-leading healthcare intelligence and clinical research organi...

Location

United Kingdom , Reading

Salary:

Not provided

iconplc

Expiration Date

Until further notice

Requirements

Bachelor degree or equivalent, preferably in a scientific or pharmaceutical discipline
At least three 2-3 years of experience in clinical supplies planning/supply chain management, with (5) years of experience in clinical supplies, clinical research or pharmaceutical development
Working knowledge of the Clinical Trial Supply process
Working knowledge of project team structure and processes
Proactive approach to work, identifying potential issues well in advance and bringing them to the attention of appropriate personnel for resolution.
Knowledge of project management and Clinical customer relationship building
Knowledge of the ‘Customers’ team structures and processes
Excellent verbal and written communication skills
Ability to influence others
Ability to multi-tasks

Job Responsibility

Manage clinical supply planning and forecasting for study protocols
Serve as member of clinical study team and/or clinical drug supply team, as assigned
Interpret relevant protocol information to develop packaging/labeling design and/or global distribution strategy
Support design and set-up of IRT system
Support financial planning for global clinical supplies, including budgeting, forecasting, and strategic planning activities for clinical trials and pharmaceutical development pipeline
Coordinate the origination, proofing and translation of clinical study labels, as required
Monitor global clinical supply inventory at the clinical site level for both IRT and traditional studies via tracking of specific milestone dates and adjusting drug distribution plan accordingly
Coordinate drug supply delivery timelines with Clinical, packaging source area(s), and indirectly with GMP laboratories, QA and Regulatory Affairs, as required
Maintain close communications with all internal-chain groups to ensure the adequate supply of clinical supplies throughout the duration of a clinical trial
Serve as ‘consultant’ for managers throughout the organization on issues related to clinical supplies and project management

What we offer

Various annual leave entitlements
A range of health insurance offerings to suit you and your family’s needs.
Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead.
Global Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized professionals who are there to support you and your family’s well-being.
Life assurance
Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others.

Fulltime

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Senior Clinical System Designer

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