clinical data scientist

Freshot Robotics - Food Automation

<p><b>Data Scientist, Clinical Research &amp; AI Data Representation (Information Specialist)</b></p><p><b>Job Overview Summary</b></p><p>We are seeking a data-driven Information Specialist or Data Scientist to leverage advanced AI and data science to transform complex clinical and healthcare information into actionable insights. This role emphasizes developing analytical solutions and AI-assisted data representation techniques to enhance clinical study optimization and accelerate drug discovery. You will drive innovation, contributing to a product roadmap that utilizes scalable infrastructure.</p><p><b>Key Responsibilities</b></p><ul><li>Clinical Data Analysis &amp; Modelling: Design and implement ML/statistical models for clinical research data (RWE, EHR, omics, clinical trials).</li><li>AI-Assisted Information Visualization: Innovate AI-driven visualization for complex clinical data, ensuring clarity for medical and research stakeholders.</li><li>Prompt Engineering &amp; Generative AI: Apply expertise in prompt engineering to guide and evaluate Generative AI/LLM applications for information extraction, summarization, and retrieval in clinical contexts.</li><li>Clinical Trial Data Strategy: Contribute to data science strategy, specifically aligning with clinical study optimization goals and regulatory requirements.</li><li>Cross-functional Collaboration: Partner with clinical, medical, and engineering teams to translate research questions and information needs into data solutions.</li><li>MLOps: Deploy, monitor, and maintain ML models in production, adhering to strict regulatory standards (GCP, HIPAA, GDPR).</li></ul><p><b>Qualifications</b></p><ul><li>Clinical &amp; Healthcare Domain: Essential: Demonstrated hands-on experience and deep understanding of clinical research, life sciences, or healthcare data.</li><li>Education &amp; Experience: Bachelor&rsquo;s degree (4-year professional degree) in Data Science, Information Science, Bioinformatics, or a related quantitative field, OR a Master's degree in a relevant field. 4+ years of relevant experience</li><li>Programming &amp; Tools: Proficiency in Python (Pandas, Scikit-learn, deep learning frameworks) and/or R, strong SQL skills.</li><li>Databricks &amp; Big Data: Extensive, hands-on experience with the Databricks platform (Databricks SQL, Databricks ML, Delta Lake) and Spark (PySpark/Scala Spark) for large-scale data processing, ETL, and feature engineering.</li><li>Prompt Engineering: Demonstrated practical experience with prompt engineering, LLMs, or related conversational AI applications.</li><li>Analytical &amp; Communication Skills: Excellent analytical, critical thinking, and problem-solving abilities. Strong communication and interpersonal skills to articulate complex clinical and AI concepts to both technical and medical teams.</li><li>Cloud Platforms: Experience with cloud-based platforms (AWS, Azure, GCP) for data storage, processing, and analytics is a plus.</li></ul><p>Job Type: Full-time</p><p>Pay: &#8377;500,000.00 - &#8377;1,200,000.00 per year</p><p>Benefits:</p><ul><li>Paid sick time</li><li>Paid time off</li><li>Provident Fund</li></ul><p>Work Location: In person</p>

Data Scientist

Pfizer

<div></div><div><div>ROLE SUMMARY</div><div>
As part of the Clinical Data Sciences group, an integral delivery unit within the Clinical Development &amp; Operations (CD&amp;O) organization, the Senior Central Testing Analyst is responsible for leading the Database Testing and validation activity at a study or asset level and performing testing of database (UAT) and ensuring that the CRFs are designed in accordance to protocol and the end users are able to enter the data as per the standards and expectation. In addition to the screen testing the Senior Central Testing Analyst will also be responsible to perform the testing of data specification to ensure that the checks are rightly programmed, appropriate and adequate as per the protocol requirement.</div><div></div><div>
ROLE RESPONSIBILITIES</div><ul><li>
Provides technical skills and knowledge to assigned work to achieve and perform activities, including but not limited to: the testing of CRF design, Database building, Acquisition &amp; Processing of electronic data, such as external eData, Lab Data and PK/PD Data; Data extraction and listing for quality review, Data Visualization; Data and Documentation Processing, CRF and Database edit checks/validation and outputs.</li><li>
Accountable for high quality and on time delivery for assigned deliverables.</li><li>
Participate in initial DM meetings with Clinical Data Scientist (CDS) to understand the expectation and scope of the study.</li><li>
Ensure work carried out in accordance with applicable SOPs and working practices.</li><li>
Understand the Protocol and provide input to Study Team on Database Design and Edit Check Specification as appropriate.</li><li>
Based on Study Data Specification (SDS) the Screen UAT has to be executed and compare the Schedule of Assessment from Protocol with Database and Provide Suggestions.</li><li>
Review the Edit Check Specification, write UAT test scripts.</li><li>
Execute the scripts and log the issues in UAT tracker and provide feedback to Study Team</li><li>
May perform peer review on programming of edit checks</li><li>
May perform check on metadata listing</li><li>
Participate in UAT feedback meetings</li><li>
Streamline/Standardize the Scripts for Standard Forms/Edit Checks</li><li>
Validation of Manual queries/Listings (Standards/Therapeutic Specific)</li><li>
Able to understand the Postproduction Changes in Database during conduct and provide clinical/technical suggestion.</li><li>
Communicates effectively to study team about suggestion and changes to database.</li><li>
Track the lessons learned and share the knowledge across the team.</li><li>
Complete all the documentation related to study and share it with study team.</li><li>
Perform testing of reports and document the same.</li><li>
Maintain a high customer satisfaction level and work with global study teams to meet objectives/timelines.</li><li>
Able to resolve conflicts, influence and communicate with key stakeholders and customers.</li><li>
Organizes own work to time to meet agreed milestones and targets; develops plans for short-term work activities on own assignments (timelines, work plans, deliverables).</li><li>
Learns and applies basic team effectiveness skills (e.g., commitment, feedback, consensus management).</li></ul><div>
QUALIFICATIONS</div><ul><li>
Demonstrated knowledge of clinical development process including knowledge and understanding of the principles of GCP</li><li>
Demonstrated knowledge of data management processes and principles in area of responsibility.</li><li>
Working knowledge of all phases of clinical trials and ability to assess and determine study requirement from protocol review</li><li>
Demonstrates strong verbal and written communication skills including ability to communicate remotely</li><li>
Minimum 7 years of relevant experience required</li><li>
Working knowledge of clinical research, FDA &amp; ICH, GCP, GCDMP, and related regulatory requirements</li><li>
Proficient experience using commercial clinical data management systems and/or EDC products (e.g., Inform preferred)</li><li>
Experience using data visualization tools (e.g. Spotfire, J-Review) preferred</li><li>
Familiarity with MedDRA/WHO-Drug</li><li>
Proficiency in the use of Microsoft Office Suite of tools (Outlook, Word, Excel, etc.)</li><li>
Bachelor&rsquo;s degree minimum requirement.</li><li>
Experience of project management skill in terms of resource management and timeline and quality control preferred.</li><li>
Experience performing testing of database and/or leading a team of testers performing the UAT activities.</li></ul>
<br>
Work Location Assignment: Hybrid<div></div><div><br>
Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates.</div><div></div>
Medical</div><div></div>

Senior Associate, Senior Central Testing Analyst

Phastar

<div>Overview:
<div><b>
THE COMPANY</b></div><div>
Phastar is a multiple award-winning global biometric Contract Research Organization (CRO) that is accredited as an outstanding company to work for by Best Companies. We partner with pharmaceutical, biotechnology and medical device organizations to provide the expertise and processes to manage and deliver on time, quality biostatistics, programming, data management and data science services. With offices across the UK, US, Germany, Denmark, Kenya, Australia, India, China and Japan, Phastar is the second largest specialized biometrics provider globally, and the largest in the UK.</div><div>
Our unique approach to data analysis, &ldquo;The Phastar Discipline&rdquo;, has led us to build a reputation for outstanding quality. With this as our core focus, we&rsquo;re looking for talented individuals who share our passion for quality and technical expertise to join our team.</div><div></div><div><b><br>
WHY PHASTAR</b></div><div></div><div><br>
Accredited as an outstanding company to work for, Phastar is committed to employee engagement, workplace satisfaction and ensuring a healthy work-life balance. We offer flexible working, part-time hours, involvement in developing company-wide initiatives, structured training and development plans, and a truly supportive, fun and friendly environment.</div><div>
We are seeking a Principal Data Scientist to support one of our pharmaceutical clients and work specifically within one of our FSP teams.</div>
Responsibilities:
<div>
Identify and build practical, high-quality solutions through the application of visualisation analytical,machine learning and artificial intelligence techniques<br>
Document, initiate and perform appropriate validation and/or QC for a project<br>
Identify, access and utilise the appropriate data to support a question such as clinical data, observational data, healthcare data<br>
Develop cross-filtering, drill-downs, faceting, bookmarking, state restore, and user-level preferences.<br>
Add new features and modules end-to-end: scope requirements, prototype, iterate with users, and productionise.<br>
Help design and build a large, modular Shiny application that visualizes TLFs (tables, listings, figures) from SDTM/clinical datasets.<br>
Run CI/CD on Github.<br>
Deploy/operate on Posit Connect (or Shiny Server Pro): access controls, scaling, monitoring.<br>
Error tracking, unit tests, UI tests, integration/performance checks.<br>
Implement export workflows (e.g., CSV/XLSX, PNG/PDF, RTF) with reproducible, versioned outputs.<br>
Add new features and modules end-to-end: scope requirements, prototype, iterate with users, and productionize.<br>
Collaborate with other functions as required<br>
Produce and validate complex outputs<br>
Identify areas where new processes are required<br>
<b>Essential:</b><br>
2&ndash;5+ years of experience building production-grade Shiny applications in R.<br>
Strong R programming fundamentals (tidyverse or data.table), Shiny modules/reactivity, and data visualization using ggplot2 or plotly.<br>
Experience with Git, code review, and automated testing.<br>
Hands-on deployment experience with Posit Connect (or equivalent platforms).<br>
Excellent communication skills and ability to collaborate with non-technical stakeholders.<br>
<b>Preferred:</b><br>
Knowledge of clinical programming standards (e.g., CDISC, SDTM, controlled terminology, and awareness of ADaM/TFLs).<br>
Experience with Python for data engineering or validation (pandas, reticulate interoperability).<br>
Familiarity with cloud platforms (AWS, Azure, or GCP) and container orchestration tools (Docker, Kubernetes).</div>
Qualifications:
<div>
Educated to PhD/Masters or Bachelor&rsquo;s degree in statistics, computational biology, bioinformatics,mathematics, computer science or a related discipline<br>
Experience within the pharmaceutical or healthcare industry<br>
Familiarity with GCP and regulatory requirements<br>
R Shiny experience required</div><div></div><div><b><br>
APPLY NOW</b></div><div>
With the world&rsquo;s eyes focused on clinical trial data, this is a fantastic time to join an award-winning specialized biometric CRO that is renowned for its technical expertise, outstanding quality and cutting-edge data science techniques. We offer flexible working, part-time hours, structured training and development plans, continuous learning opportunities, and a competitive salary and benefits package. We&rsquo;re committed to ensuring our employees achieve a healthy work-life balance, within a supportive, fun and friendly working environment.</div><div></div><div><br>
Should you feel that you have the right skill set and motivations for this position, please apply!</div><div></div><div><br>
Phastar is committed to the principles and practices of equal opportunities and to encouraging the establishment of a diverse workforce. It is our policy to employ individuals on the basis of their suitability for the work to be performed and their potential for development, regardless of age, sex, race, colour, nationality, ethnic or national origin, disability, marital status, pregnancy or maternity, sexual orientation, gender reassignment, religion, or belief. This includes creating a culture that fully reflects our commitment to equal opportunities for all.</div><div></div><div><b><br>
Important notice to Employment businesses/Agencies</b></div><div></div><div><br>
Phastar does not accept referrals from employment businesses and/or employment agencies in respect of the vacancies posted on this site. All employment businesses/agencies are required to contact Phastar's Head of Talent Acquisition to obtain prior written authorization before referring any candidates to Phastar. The obtaining of prior written authorization is a condition precedent to any agreement (verbal or written) between the employment business/ agency and Phastar. In the absence of such written authorization being obtained any actions undertaken by the employment business/agency shall be deemed to have been performed without the consent or contractual agreement of Phastar. Phastar shall therefore not be liable for any fees arising from such actions or any fees arising from any referrals by employment businesses/agencies in respect of the vacancies posted on this site.</div></div><div></div>

Principal Data Scientist

Celerion

<div><div>Celerion is committed to swift, exceptional clinical research through translational medicine. Every day, we use our experience, agility, and innovative research strategies to help get drugs to market faster.</div><div></div><div><br>
Are you looking for an opportunity to support a business creating life-saving treatments? If so, we can't wait to meet you!</div><div>
</div><div>
We are looking for a performance-oriented, innovative and self-motivated team player to join our Clinical Data Sciences team as a full-time <b>Electronic Data Capture (EDC) Database Developer / Clinical Programmer</b>. You will be responsible for administration of EDC Database including evaluation, analysis, design and/ or recommendations to achieve goals and excellent results in a fast-paced, ever-changing environment.</div><div>
</div><div>
This is a <b>full time, remote</b> opportunity, but may travel for training and key meetings.</div><div>
</div><div>
As an <b>EDC Database Developer,</b> you will build and administer EDC trials for client contracted projects including protocol/requirements evaluation, electronic case report form (eCRF) design and build with corresponding edits. This role will have technical interaction with vendors that are supporting the applications and troubleshoot/ escalate problems on systems to appropriate partners. This role will provide expert guidance to the design, development, validation, implementation and maintenance of study set-up. Additionally, this role will manage the deployment of EDC trials and set up interface connections between EDC and other systems.</div><br>
<div></div>
<h3 class="jobSectionHeader"><b>
In this role you will:</b></h3><ul><li>
Serve as a subject matter expert in Veeva Clinical Data Management Suite (CDMS), including Veeva Electronic Data Capture (EDC) and Veeva Clinical Database (CDB)</li><li>
Perform all activities related to eCRF design and EDC build programming for assigned projects</li><li>
Perform EDC edit check programming for assigned projects based on edit check specifications for both simple and complex edit checks</li><li>
Create test data to verify both screen design and edit check programming prior to deploying to User Acceptance Testing (UAT)</li><li>
Set up test environments and coordinate project team members for execution of test scripts</li><li>
Program and configure listings and reports using clinical reporting tools such as Veeva Clinical Database (CDB)</li><li>
Ensure secure and high-integrity database imports from vendor transfers using Celerion data transfer standards</li><li>
Assist with the validation of upgrades to hardware/ software including validation documentation development, review and execution.</li><li>
Maintain global clinical trial database standards (CDISC)</li></ul><h3 class="jobSectionHeader"><b>
Requirements:</b></h3><ul><li>
Bachelor&rsquo;s degree in a related field preferred</li><li>
3 years of clinical data management experience</li><li>
Ability to program using SQL required</li><li>
Experience with EDC systems (i.e. Veeva CDMS, Medidata RAVE, etc.)</li><li>
Experience with Veeva EDC and Veeva CDB preferred
</li><li>Proficient computer skills with understanding of clinical systems and data administration</li><li>
Must be organized, an effective written and oral communicator</li><li>
Must have the ability to multi-task, within a fast-paced environment, and build strong relationships</li></ul><div><b>
Celerion Values: Integrity Trust Teamwork Respect</b></div><div></div><div><br>
Celerion is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, age, sexual orientation, gender identity, genetic information, marital status, qualified protected veteran status, or disability.</div>
<p>
We may use artificial intelligence (AI) tools to support parts of the hiring process, such as reviewing applications, analyzing resumes, or assessing responses. These tools assist our recruitment team but do not replace human judgment. Final hiring decisions are ultimately made by humans. If you would like more information about how your data is processed, please contact us.</p></div>

EDC Developer / Programmer

Hoag Health System

<div><b>Primary Duties and Responsibilities
</b><p>The Clinical Lab Scientist II (CLS II) performs a range of standard and technically demanding procedures and analysis on patient specimens in one or more clinical laboratory disciplines. This role recognizes critical and significant findings, reports test results, and maintains records of patient tests. Also, recognizes technical, instrumental, or physiological problems that could adversely affect tests or results, resolves, and documents. Performs calibration and maintenance of laboratory instruments. Adheres to quality control protocols to ensure accuracy of results. Monitors the accuracy and precision of all laboratory tests personally performed. Actively participates in continuing education programs. Communicates technical and general information to manager and medical staff.
</p><p>In addition to the above, the CLSII analyzes data for trends, ensures, departmental standard operating procedures and competency documents reflecting current practice, and documents nonconforming events. May act as lead on weekends or other periods of reduced staffing.
</p><p>Projects an image of professionalism in communication, appearance and conduct. Supports the laboratory mission. Participates in the continuous quality improvement process. Maintains a working knowledge of departmental standard operating procedures. This knowledge may include the use of specialized instrumentation, quality control requirements, and preventative maintenance. Performs other duties as assigned.</p></div>
<br><div></div>
<br><div><p><b>Education and Experience
</b></p><ul><li>Baccalaureate Degree in medical technology or related science required.
</li><li>Two to three years relevant clinical laboratory experience as an CLS required.
</li></ul><p><b>License Required
</b></p><p>Must meet and maintain current State of California licensure requirements for one of the following.
</p><ul><li>Clinical Laboratory Scientist
</li><li>One of the following Limited Clinical Laboratory Scientist:
<ul><li>CHEMISTRY - Clinical Chemist Scientist
</li><li>HEMATOLOGY/URINALYSIS - Hematologist Scientist
</li><li>TRANSFUSION SERVICE - Clinical Immunohematologist Scientist
</li><li>MICROBIOLOGY - Clinical Microbiologist Scientist / Public Health Microbiologist</li></ul></li></ul></div><p></p>

Clinical Lab Scientist II : Orange Coast Women's

Stryker

<div><h3 class="jobSectionHeader"><b>Why join Stryker?</b></h3>
Looking for a place that values your unique talents? Discover Stryker's award-winning culture.<br>
We are proud to offer you our total rewards package which includes bonuses, healthcare, insurance benefits, retirement programs, wellness programs, as well as service and performance awards &ndash; not to mention various social and recreational activities, all of which are location specific.<h3 class="jobSectionHeader"><b>
Job description</b></h3>
We are excited to be named one of the World&rsquo;s Best Workplaces by Fortune Magazine!
<br>
We are proud to offer you our total rewards package which includes bonuses, healthcare, insurance benefits, retirement programs, wellness programs, as well as service and performance awards &ndash; not to mention various social and recreational activities, all of which are location specific.<br>
<div><h2 class="jobSectionHeader"><b>
What you will do:</b></h2><p></p><p>
This position leads the design and execution of regulatory-grade and commercial RWE studies to support clinical evidence needs. Working with key stakeholders, the role will execute on key RWE deliverables and establish standards and best practices for RWE study design and reporting as an essential part of the clinical evidence generation strategy for Stryker&rsquo;s product portfolio.</p><ul><li><p>
Lead design and execution of RWE studies in close collaboration with internal stakeholders from Clinical Strategy, Medical Affairs, and Clinical Data Science.</p></li><li><p>
Author and/or oversee development of study protocols, reports, conference abstracts, and peer-reviewed publications using RWD and collaborate cross-functionally to integrate RWD into global publication strategies</p></li><li><p>
Ensure scientific rigor and serve as a methodology expert for real-world evidence generation; select and implement appropriate analytic methods aligned to research needs</p></li><li><p>
Collaborate closely with data management and biostatistics functions to ensure data quality and deliver robust data analyses utilizing scientifically valid and accepted methodology for RWD</p></li><li><p>
Conduct feasibility assessment of relevant data sources for specific devices and indications to ensure data is fit-for-purpose</p></li><li><p>
Identify and evaluate new RWD sources</p></li><li><p>
Ensure quality and performance standards for RWE projects are realistic and attained, and studies are conducted in line with quality/compliance framework</p></li><li><p>
Identifies areas of improvement with RWE processes and procedures, develops and implements best practices, and works to improve efficiencies and effectiveness. Participate in cross-functional and cross-divisional initiatives regarding RWE</p></li></ul><h2 class="jobSectionHeader"><b>
What you need:</b></h2><ul><li><p>
3-6 years relevant experience in epidemiology and/or observational research in academia, a contract research organization, and/or the medical device or pharmaceutical industry</p></li><li><p>
Hands-on experience with real-world data (RWD) sets such as patient registries, electronic medical records, hospital billing data, and insurance claims databases and familiarity with relevant medical coding vocabularies (e.g., ICD, CPT, HCPCS, LOINC)</p></li></ul><ul><li><p>
A sophisticated understanding and ability to analyze and interpret quantitative data is required together with working knowledge of RWE/observational study design and methodology</p></li><li><p>
Experience using standard statistical software (e.g., SAS, R, Stata) and/or demonstrated ability to collaborate closely with statistical programmers; understanding of advanced statistical methods utilized for RWD analysis (e.g., propensity score matching)</p></li><li><p>
Excellent oral and written communication skills, experience authoring study protocols, study reports, and peer-reviewed publications using RWD preferred</p></li><li><p>
Strong organizational skills, with ability to effectively and efficiently handle multiple tasks simultaneously, with precision, and to adapt to changes in responsibilities and workloads</p></li><li><p>
Must be professional, possess a high degree of urgency and self-motivation, and have a strong work ethic</p></li><li><p>
Must possess a high degree of integrity and ability to maintain confidentiality with HIPAA and GDPR guidelines, and other confidential information</p></li></ul></div><p></p>
Stryker is a global leader in medical technologies and, together with its customers, is driven to make healthcare better. The company offers innovative products and services in MedSurg, Neurotechnology, Orthopaedics and Spine that help improve patient and healthcare outcomes. Alongside its customers around the world, Stryker impacts more than 150 million patients annually.</div>

Senior Analyst- Epidemiologist, Real-World Evidence (RWE)

Deciphera Pharmaceuticals

<div>
 <strong>
  Job Description
  <br/>
  <br/>
 </strong>
 The Pharmacovigilance Scientist serves an integral role in safety data analyses for assigned investigational and/or marketed product(s) in partnership with the Safety Physician. The Pharmacovigilance Scientist is expected to be equally effective working collaboratively and independently. She/he will support activities such as signal management, aggregate reports, RMP development, ad hoc safety query responses, literature surveillance, and other safety analyses; and must ensure deliverables are of high quality and are completed according to required timelines. For investigational products, this role will contribute to safety review and analysis for clinical trial documents. The Pharmacovigilance Scientist will also support the maintenance of relevant SOPs, Work Instructions, and other documents.
 <br/>
 <br/>
 The successful candidate will have demonstrated adequate prior experience of the above responsibilities. Key indicators of success in this role include accountability, attention to detail, appropriate prioritization, management of assigned projects with quality and timeliness, and effective communication.
 <br/>
 <br/>
 This position will report to the Sr. Pharmacovigilance Scientist and will be located in the Waltham, MA office/Remote.
 <br/>
 <br/>
 <strong>
  What You&rsquo;ll Do
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Coordinate and document signal management activities with the product Safety Physician. This includes performing signal evaluations and drafting signal evaluation reports.
  </li>
  <li>
   Prepare aggregate safety reports (e.g. DSURs, PADERs, PBRERs), including project management, database requests, data analysis, report authoring, assimilating information from other groups, review coordination, and quality checks.
  </li>
  <li>
   Support RMP updates and REMS reports as appropriate.
  </li>
  <li>
   Perform literature surveillance for marketed and investigational products .
  </li>
  <li>
   Prepare materials for Safety Committee meetings in conjunction with the product Safety Physician and document/archive meeting minutes and materials.
  </li>
  <li>
   Coordinate responses for ad hoc safety queries in conjunction with the Safety Physician and other cross-functional experts, including data analysis and authoring, as applicable.
  </li>
  <li>
   Support review and analysis of safety content for study protocols, CRFs, IB/RSIs, ICFs, SMPs, CSRs, DMC meetings, and coding reviews, as applicable.
  </li>
  <li>
   Demonstrate knowledge and stay up to date to ensure compliance with current and applicable global PV regulations and guidelines (e.g., CIOMS, EMA, FDA, ICH, etc.)
  </li>
  <li>
   Contribute to process improvement and consistency of cross-product processes.
  </li>
  <li>
   Maintain inspection readiness.
  </li>
  <li>
   Perform other tasks as assigned or required.
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Qualifications
  <br/>
  <br/>
 </strong>
 <strong>
  What You&rsquo;ll Bring:
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   1+ years relevant medical, scientific/clinical, or pharmaceutical experience, including experience in drug safety serving in a PV Scientist or similar role.
  </li>
  <li>
   Advanced degree (PharmD, RN, MD, PhD, MPH, NP, MS).
  </li>
  <li>
   Demonstrated experience in analysis and interpretation of medical and scientific data.
  </li>
  <li>
   Excellent oral and written communication skills.
  </li>
  <li>
   Demonstrated ability to work effectively in a team environment (including Safety, Clinical Development, Medical Affairs, Clinical Operations, Regulatory, Biostatistics, etc.) as well as independently.
  </li>
  <li>
   Ability to apply clinical judgment to interpret case information.
  </li>
  <li>
   Knowledge of pharmacovigilance and drug development, including knowledge of applicable clinical trial and post-marketing safety regulations.
  </li>
  <li>
   Familiarity with case processing, expedited reporting rules, and safety database concepts.
  </li>
  <li>
   Proficiency with Microsoft Office Suite and Argus Safety systems.
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Additional Information
  <br/>
  <br/>
 </strong>
 Deciphera is committed to fair and equitable compensation practices. The base salary pay range for this role is $135,000 - $189,000. Actual compensation packages will depend on various factors, including, but not limited to depth of experience, education, skillset, overall performance and/or location.
 <br/>
 <br/>
 Deciphera believes in providing a competitive compensation and benefits package to all employees. Our base salary is just one component of Deciphera&rsquo;s competitive total rewards strategy that also includes annual performance bonus, a long-term incentive plan, full range of benefits and other incentive compensation plans (if applicable)
 <br/>
 <br/>
 <strong>
  Benefits
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Competitive salary and annual bonus.
  </li>
  <li>
   Comprehensive benefits package including medical, dental, vision insurance, 401(k) retirement plan with company match, and more.
  </li>
  <li>
   Generous parental leave and family planning benefits.
  </li>
  <li>
   Outstanding culture and opportunities for personal and professional growth.
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Apply Now:
 </strong>
 Join us in our mission to improve the lives of people with cancer. Apply today to become a part of our dynamic team!
 <br/>
 <br/>
 <strong>
  EQUAL EMPLOYMENT OPPORTUNITY INFORMATION
  <br/>
  <br/>
 </strong>
 Deciphera is committed to equal employment opportunity and values diversity. To ensure that we comply with reporting requirements, we invite you complete the confidential survey at the end of this application. Providing this information is optional. It will not be accessible or used in the hiring process, and has no effect on your opportunity for employment. This information will also be treated confidentially. We are committed to make all hiring decisions and other employment decisions on a non-discriminatory basis.
</div>


Pharmacovigilance Scientist

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