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Clinical Data Management Summer Intern

Boehringer Ingelheim

Clinical Data Management Summer Intern

Ridgefield, CT
Internship
Paid
  • Responsibilities

    Clinical Data Management Summer Internship Job Description: BoehringerIngelheim (BI) is currently seeking a talented and innovative Intern to join our Biostatistics andData Sciences_ _departmentlocated at our Ridgefield, Connecticut facility. As an intern, you will supportthe clinical research development process in the field of clinical datamanagement (CDM). The intern will learn diverse aspects of the clinical triallandscape and apply learned clinical data management principles all within the standard setting asdocumented through BI SOPs. It isan excellent opportunity to learn about the clinical trial data lifecycle fromthe beginning. As an employee of BI, you will actively contribute to thediscovery, development and delivery of our products for our patients andcustomers. Our global presence provides opportunity for all employees tocollaborate internationally, offering visibility and opportunity to directlycontribute to the companies' success. We realize that our strength andcompetitive advantage lie with our people. We support our employees in a numberof ways to foster a healthy working environment, meaningful work, diversity andinclusion, mobility, networking and work-life balance. Our competitivecompensation and benefit programs reflect BIs high regard for our employeesand in addition we have a strong mentoring program. **Type of Student: ** Pursuing a BS or MS in LifeScience, Computer Science, Data Science, Project Management or a related degreeprogram preferred. Duties & Responsibilities: * Reviews and gives inputinto the creation and maintenance of all essential data managementdocumentation including Case Report Form (CRF) specifications, eCRFs, annotatedeCRF, eCRF completion guidelines, Data Management Plans (detailing completedata management processes throughout clinical studies), Data Transferspecifications and Data Review Plans, in accordance with the protocol, company andproject data standards. * Reviews and gives inputinto external data specifications (non-CRF data) from vendors or other internaldepartments into the clinical trial database. * Reviews and gives inputinto established conventions and quality expectations for clinical data andplans and tracks the content, format, completeness, quality and timing of thetrial data collection process and other CDM deliverables via data analyticsthroughout the conduct of a trial. * Under the direction of theTrial Data Manager (TDM) works to ensure that the trial database can be closedaccording to the planned timelines and quality (as applicable). * Defines or reviews the SDTM(Study Data Tabulation Model) data to assure compliance together with the TrialData manager (TDM), Project Data Manager (PDM) and the Standards team. * Attends applicable TrialOversight Meetings (TOMs) / Medical and Quality Review Meetings (MQRMs) andother trial team meetings. * As applicable, assist TDMwith trial oversight and documentation. * Ad hoc projects asrequested, eg research data curation for Machine Learning (ML) initiatives withinCDM. Requirements: * Must be pursuing a BS or MSin Life Science, Computer Science, Data Science, Project Management or arelated degree program at an accredited institution * Must havecompleted 12 credit hours within a related major and/or other relatedcoursework. * Overall,cumulative GPA (from last completed quarter) must be at least 3.0 (on a 4.0 scale)or better and must be a student in good academic standing * Goodwritten and oral communications skills in the English language * Knowledgein basic medicine terminology is beneficial * Goodorganizational skills, problem-solving abilities, time management skills andinitiative is desired as well as flexibility and ability to work on severalassignments simultaneously. Must be ableto work independently as well as part of a team * Mustbe precise, detail oriented, and able to detect subtle inconsistencies in thedata EligibilityRequirements: * Must be legally authorized to work in the United Stateswithout restriction. * Must be willing to take a drug test and post-offerphysical (if required) * Must be 18 years of age or older Who We Are: At Boehringer Ingelheim we create value throughinnovation with one clear goal: to improve the lives of patients. We developbreakthrough therapies and innovative healthcare solutions in areas of unmetmedical need for both humans and animals. As a family owned company we focus onlong term performance. We are powered by 50.000 employees globally whonurture a diverse, collaborative and inclusive culture. Learning anddevelopment for all employees is key because your growth is our growth. Want to learn more? Visit boehringer- ingelheim.comand join us in our effort to make more health. Boehringer Ingelheim,including Boehringer Ingelheim Pharmaceuticals, Inc., Boehringer Ingelheim USA,Boehringer Ingelheim Animal Health USA, Inc., Merial Barceloneta, LLC andBoehringer Ingelheim Fremont, Inc. is an equal opportunity and affirmativeaction employer committed to a culturally diverse workforce. Allqualified applicants will receive consideration for employment without regardto race; color; creed; religion; national origin; age; ancestry; nationality;marital, domestic partnership or civil union status; sex, gender identity orexpression; affectional or sexual orientation; disability; veteran or militarystatus, including protected veteran status; domestic violence victim status;atypical cellular or blood trait; genetic information (including the refusal tosubmit to genetic testing) or any other characteristic protected by law. including protected veteran status; domestic violencevictim status; atypical cellular or blood trait; genetic information (includingthe refusal to submit to genetic testing) or any other characteristic protectedby law. Boehringer Ingelheim is firmly committed to ensuring asafe, healthy, productive and efficient work environment for our employees,partners and customers. As part of that commitment, Boehringer Ingelheimconducts pre- employment verifications and drug screenings. **Primary Location: **Americas-US-CT-Ridgefield **Work Locations: ** **Job: **Internships **Organization: **Boehringer Ingelheim Vetmedica, Inc. **Schedule: **Full-time

  • Industry
    Manufacturing