Urwah Admin

Vertex Pharmaceuticals

<div><p><b>Job Description
</b></p><div><div><p><b>Employer </b>: Vertex Pharmaceuticals Incorporated<br>
</p></div><p></p><div><p><b>JOB </b><b>TITLE </b>: Principal Clinical Programmer<br>
</p></div><p></p><div><p><b>LOCATION </b>: 50 Northern Ave. , Boston, MA, 02110<br>
</p></div><p></p><div><p><b>OPENINGS: </b>1<br>
</p></div><p></p><div><p><b>DUTIES </b><b>:
</b></p></div><div><ul><li><p>Utilize SAS and other supporting tools to design, write, validate , and maintain programs to meet specifications in a quality, timely and productive manner following standard development procedures.
</p></li></ul></div><div><ul><li><p>Solid understanding of Clinical data warehouse platform ( Elluminate ), act as a subject matter expert for all the end users.
</p></li></ul></div><div><ul><li><p>Excellent programming skills to perform all the report development, data analytics and configuration in Elluminate application.
</p></li></ul></div><div><ul><li><p>Generate and maintain all required documentation, including the development of specifications, coding, and validation efforts in support of clinical studies.
</p></li></ul></div><div><ul><li><p>Acts as a technical resource, supporting clinical programming and data management staff in their effective use of SAS for data review.
</p></li></ul></div><div><ul><li><p>Ensure high-quality deliverables by providing senior review of study level, program level, and multi study core deliveries for accuracy.
</p></li></ul></div><div><ul><li><p>Attend sponsor audits and assist with in-progress audits.
</p></li></ul></div><div><ul><li><p>Provide application administration and technical support on core business packages including CRF, SAS, and supplemental packages such as migration mentor review, reporting tools, and custom functions.
</p></li></ul></div><div><ul><li><p>Serve on program teams to coordinate and lead development activities for clinical programming projects.
</p></li></ul></div><div><ul><li><p>Keep those responsible for project management informed of any issues that might impact project target dates, scope, or budget and proactively escalates potential problems, including resourcing.
</p></li></ul></div><div><ul><li><p>Assist in sponsor and internal audits, and regulatory inspections.
</p></li></ul></div></div><div><div><ul><li><p>Monitor the scope of work to actual work, alerting management of potential change orders.
</p></li></ul></div><div><ul><li><p>Manage and execute the change order to completion.
</p></li></ul></div><div><ul><li><p>Provide input and support details for change orders.
</p></li></ul></div><div><ul><li><p>Collaborate with clients, peers, lead programmers, project teams and requestors to clarify and finalize specifications, and use expanded technical skills to meet evolving project needs.<br>
</p></li></ul></div><p></p><div><p>Telecommuting permitted .<br>
</p></div><p></p><div><p><b>REQUIREMENTS </b><b>: </b>Employer will accept a Bachelor's degree or foreign equivalent in engineering, computer science or a related field and 6 years of experience in the job offered or in a Principal Clinical Programmer -related occupation.<br>
</p></div><p></p><div><p>Position requires demonstrable experience in the following:<br>
</p></div><p></p><div><p>High proficiency in Programming languages in CDMS like SAS and SQL Plus and good knowledge of data standards, such as CDISC, STDM and CDASH.
</p></div><div><p>Solid understanding of Elluminate and also possess excelling programming skills in to develop reports and also design data analytics in Elluminate .
</p></div><div><p>High proficiency in Clinical Data Management procedures including good knowledge of Good Clinical Practices (GCP), 21 CFR part 11 and other regulatory requirements.
</p></div><div><p>Significant, demonstrated experience with clinical programming, clinical data management, CRO industry and data reporting along with programming languages such as SAS.
</p></div><div><p>Proven ability to independently determine the most appropriate methods and procedures across Clinical Data Management projects.
</p></div><div><p>Interact with the end users of the CDMS (Clinical management systems) and convert their reporting requirements into programming specifications.<br>
</p></div><p></p><div><p>Rate of Pay: $161803.00 - $204200.00<br>
</p></div></div><p></p><div><p><b>CONTACT: </b>Send Resume to futuretalent @vrtx.com . Reference 12140.763 . EOE.<br>
</p></div><p></p><div><p>#LI-DNI
</p></div><p></p><p><b>Pay Range:
</b></p>$0 - $0
<p></p><p><b>Disclosure Statement:
</b></p><div><div><div><div><p>The range provided is based on what we believe is a reasonable estimate for the base salary pay range for this job at the time of posting. This role is eligible for an annual bonus and annual equity awards. Some roles may also be eligible for overtime pay, in accordance with federal and state requirements. Actual base salary pay will be based on a number of factors, including skills, competencies, experience, and other job-related factors permitted by law.
</p><p></p><p>At Vertex, our Total Rewards offerings also include inclusive market-leading benefits to meet our employees wherever they are in their career, financial, family and wellbeing journey while providing flexibility and resources to support their growth and aspirations. From medical, dental and vision benefits to generous paid time off (including a week-long company shutdown in the Summer and the Winter), educational assistance programs including student loan repayment, a generous commuting subsidy, matching charitable donations, 401(k) and so much more.
</p></div></div></div></div><p></p><p><b>Flex Designation:
</b></p>Remote-Eligible
<p></p><p><b>Flex Eligibility Status:
</b></p><p>In this Remote-Eligible role, you can choose to be designated as:
<br>
1. <b>Remote </b>: work remotely five days per week and come into the office on occasion &ndash; you&rsquo;re always welcome on-site; <b>or select
</b><br>
2. <b>Hybrid </b>: work remotely up to two days per week; <b>or select
</b><br>
3. <b>On-Site </b>: work five days per week on-site with ad hoc flexibility.
</p><p>Note: The Flex status for this position is subject to Vertex&rsquo;s Policy on Flex @ Vertex Program and may be changed at any time.
</p><p></p><p>#LI-Remote
</p><p><b>Company Information
</b></p><p>Vertex is a global biotechnology company that invests in scientific innovation.
</p><p></p><p>Vertex is committed to equal employment opportunity and non-discrimination for all employees and qualified applicants without regard to a person's race, color, sex, gender identity or expression, age, religion, national origin, ancestry, ethnicity, disability, veteran status, genetic information, sexual orientation, marital status, or any characteristic protected under applicable law. Vertex is an E-Verify Employer in the United States. Vertex will make reasonable accommodations for qualified individuals with known disabilities, in accordance with applicable law.
</p><p></p><p>Any applicant requiring an accommodation in connection with the hiring process and/or to perform the essential functions of the position for which the applicant has applied should make a request to the recruiter or hiring manager, or contact Talent Acquisition at ApplicationAssistance@vrtx.com</p></div>

Principal Clinical Programmer

<div>
 <strong>
  Job Description
  <br/>
  <br/>
 </strong>
 <strong>
  General Summary:
  <br/>
  <br/>
 </strong>
 The Pharmacology Research Scientist works with a high degree of independence and is adept at conceptually outlining studies to design, execute and interpret assays to study the action of compounds on in vitro or in vivo disease biology. Completes work in a resourceful, self-suf&filig;cient manner and is able to design alternative approaches to achieve desired outcomes. Keeps current on the scienti&filig;c literature relevant to his/her scienti&filig;c methodology or &filig;eld(s) of technical expertise. This level captures both the Research organization&rsquo;s entry level for staff with a research doctoral degree (PhD) and the advanced experimental expert leading one or more critical laboratory functions with high impact on drug discovery projects.
 <br/>
 <br/>
 <strong>
  Key Duties And Responsibilities
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Designs and conducts elaborate, conceptually connected, multi-component experiments
  </li>
  <li>
   Collates and interprets complex data systematically, and synthesizes results into a cohesive body of conclusions or recommendations to guide Project decisions and new research activities
  </li>
  <li>
   Exercises solid judgment to prioritize studies, considering feasibility and Project impact
  </li>
  <li>
   Performs advanced and/or complex experimental troubleshooting
  </li>
  <li>
   Scours relevant scienti&filig;c literature and routinely incorporates new insights into research activities
  </li>
  <li>
   Identi&filig;es, prioritizes and introduces relevant emerging technologies in his/her &filig;eld of expertise to advance the existing technology platforms and create/maintain a competitive advantage
  </li>
  <li>
   Explores the feasibility of applying new scienti&filig;c principles/concepts or implements and validates novel experimental approaches and technologies to achieve project goals
  </li>
  <li>
   Contributes signi&filig;cantly to patent and/or publication preparation
  </li>
  <li>
   Independently prepares study presentations and presents experimental conclusions at internal Group/Department or Project Team research meetings
  </li>
  <li>
   Performs other duties as assigned
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Knowledge And Skills
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Designs and executes complex, challenging experiments that measure the action of compounds on in vitro or in vivo disease biology assays.
  </li>
  <li>
   A broad working knowledge of fundamental pharmacology principles.
  </li>
  <li>
   Demonstrates astute understanding of his/her own discipline and the relevant literature
  </li>
  <li>
   Maintains a high level of knowledge related to current developments in the scienti&filig;c Project &filig;eld
  </li>
  <li>
   Displays proven productivity and experimental creativity, and effective dissemination of ideas
  </li>
  <li>
   Demonstrates effective, self-suf&filig;cient communication skills, especially in peer-directed presentations
  </li>
  <li>
   Demonstrates awareness of other Project-related disciplines and an understanding of general concepts and some experimental detail within those areas
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Education And Experience
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Bachelor's degree in in vitro or in vivo pharmacology or related biological sciences
  </li>
  <li>
   Typically requires a PhD and 0-3 years of experience or,
  </li>
  <li>
   Typically requires a Masters degree and 3 years of experience or,
  </li>
  <li>
   Typically requires a Bachelors degree and 6 years of experience
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Pay Range
  <br/>
  <br/>
 </strong>
 $105,600 - $158,400
 <br/>
 <br/>
 <strong>
  Disclosure Statement
  <br/>
  <br/>
 </strong>
 The range provided is based on what we believe is a reasonable estimate for the base salary pay range for this job at the time of posting. This role is eligible for an annual bonus and annual equity awards. Some roles may also be eligible for overtime pay, in accordance with federal and state requirements. Actual base salary pay will be based on a number of factors, including skills, competencies, experience, and other job-related factors permitted by law.
 <br/>
 <br/>
 At Vertex, our Total Rewards offerings also include inclusive market-leading benefits to meet our employees wherever they are in their career, financial, family and wellbeing journey while providing flexibility and resources to support their growth and aspirations. From medical, dental and vision benefits to generous paid time off (including a week-long company shutdown in the Summer and the Winter), educational assistance programs including student loan repayment, a generous commuting subsidy, matching charitable donations, 401(k) and so much more.
 <br/>
 <br/>
 <strong>
  Flex Designation
  <br/>
  <br/>
 </strong>
 On-Site Designated
 <br/>
 <br/>
 <strong>
  Flex Eligibility Status
  <br/>
  <br/>
 </strong>
 In this
 <strong>
  On-Site
 </strong>
 designated role, you will work
 <strong>
  five days per week on-site
 </strong>
 with ad hoc flexibility.
 <br/>
 <br/>
 Note: The Flex status for this position is subject to Vertex&rsquo;s Policy on Flex @ Vertex Program and may be changed at any time.
 <br/>
 <br/>
 <strong>
  Company Information
  <br/>
  <br/>
 </strong>
 Vertex is a global biotechnology company that invests in scientific innovation.
 <br/>
 <br/>
 Vertex is committed to equal employment opportunity and non-discrimination for all employees and qualified applicants without regard to a person's race, color, sex, gender identity or expression, age, religion, national origin, ancestry, ethnicity, disability, veteran status, genetic information, sexual orientation, marital status, or any characteristic protected under applicable law. Vertex is an E-Verify Employer in the United States. Vertex will make reasonable accommodations for qualified individuals with known disabilities, in accordance with applicable law.
 <br/>
 <br/>
 Any applicant requiring an accommodation in connection with the hiring process and/or to perform the essential functions of the position for which the applicant has applied should make a request to the recruiter or hiring manager, or contact Talent Acquisition at ApplicationAssistance@vrtx.com
 <br/>
 <br/>
</div>


Pharmacology Research Scientist

Join Vertex Pharmaceuticals and explore 2   exciting career opportunities. They're hiring for various roles with options for remote or on-site work. Apply today and become part of their innovative team.

Vertex Pharmaceuticals

ABOUT_COMPANY

Principal Clinical Programmer

Pharmacology Research Scientist