Data Scientist – Clinical Trials (TAVR)

Posted 12 months ago Data Scientist – Clinical Trials (TAVR) MiRus is an innovative healthcare company with a growing portfolio of cardiovascular and orthopedic products and deep proprietary technology in both implants and procedural solutions. MiRus was started by a team of experienced entrepreneurs with a history of creating disruptive technologies and very successful, highly valued companies. Job Summary We offer competitive compensation, options, and full benefits. We are seeking a skilled Data Scientist to join our team supporting a pivotal TAVR clinical trial. The role focuses on managing, analyzing, and interpreting complex clinical datasets to ensure data integrity, quality, and regulatory compliance. The Data Scientist will work closely with clinical teams, biostatisticians, and CRAs to support trial endpoints, reporting, and submission-ready datasets. Responsibilities ♦ Develop, maintain, and manage clinical trial datasets in alignment with trial protocols. ♦ Perform data cleaning, validation, and quality checks to ensure integrity and compliance. ♦ Support statistical analysis, data visualization, and generation of trial reports. ♦ Collaborate with clinical teams and CRAs to resolve data queries and clarify endpoints. ♦ Ensure datasets meet regulatory standards (CDISC, SDTM, ADaM) for FDA/EMA submissions. ♦ Build dashboards or analytics tools to monitor trial progress and outcomes. ♦ Apply advanced analytics or modeling techniques to explore trends, patient outcomes, or predictive insights. ♦ Document processes, assumptions, and analysis methods according to GCP and internal SOPs. Key Qualifications ♦ Advanced degree in Data Science, Biostatistics, Computer Science, or related field. ♦ Experience in clinical trial data management; preferably in cardiology or medical device trials. ♦ Strong programming skills in SAS, R, Python, and database management (SQL, Oracle, Medidata, REDCap). ♦ Familiarity with CDISC standards (SDTM, ADaM) and FDA/EMA regulatory requirements. ♦ Experience with data visualization and reporting tools (Tableau, Power BI, or similar) ♦ Strong problem-solving skills and ability to interpret complex clinical datasets. ♦ Excellent communication and collaboration skills with cross-functional teams. Requirements ♦ Ability to work onsite full-time. ♦ Prior experience working in regulated clinical trial environments (GCP, FDA). ♦ Strong attention to detail and ability to document all analyses for regulatory review. ♦ Comfortable working in a fast-paced, high-stakes clinical trial setting. ♦ Ability to collaborate effectively with clinicians, statisticians, and project teams. Benefits MiRus offers competitive compensation, options, full benefits, and relocation assistance. ♦ 401(k) ♦ Dental insurance ♦ Vision insurance ♦ Disability insurance ♦ Employee assistance program ♦ Flexible spending account or Health Savings Account ♦ Health insurance ♦ Life insurance ♦ Paid time off Schedule ♦ Monday to Friday (8am – 5pm) Work Location: ♦ Marietta, GA ♦ Position may require domestic travel up to 10%, however this is an in-house position. Interested ?Please complete the contact information below and submit your resume to [email protected] Apply For This Job Name* Email* A valid email address is required. Phone* United States+1 United Kingdom+44 Afghanistan (‫افغانستان‬‎)+93 Albania (Shqipëri)+355 Algeria (‫الجزائر‬‎)+213 American Samoa+1 Andorra+376 Angola+244 Anguilla+1 Antigua and Barbuda+1 Argentina+54 Armenia (Հայաստան)+374 Aruba+297 Australia+61 Austria (Österreich)+43 Azerbaijan (Azərbaycan)+994 Bahamas+1 Bahrain (‫البحرين‬‎)+973 Bangladesh (বাংলাদেশ)+880 Barbados+1 Belarus (Беларусь)+375 Belgium (België)+32 Belize+501 Benin (Bénin)+229 Bermuda+1 Bhutan (འབྲུག)+975 Bolivia+591 Bosnia and Herzegovina (Босна и Херцеговина)+387 Botswana+267 Brazil (Brasil)+55 British Indian Ocean Territory+246 British Virgin Islands+1 Brunei+673 Bulgaria (България)+359 Burkina Faso+226 Burundi (Uburundi)+257 Cambodia (កម្ពុជា)+855 Cameroon (Cameroun)+237 Canada+1 Cape Verde (Kabu Verdi)+238 Caribbean Netherlands+599 Cayman Islands+1 Central African Republic (République centrafricaine)+236 Chad (Tchad)+235 Chile+56 China (中国)+86 Christmas Island+61 Cocos (Keeling) Islands+61 Colombia+57 Comoros (‫جزر القمر‬‎)+269 Congo (DRC) (Jamhuri ya Kidemokrasia ya Kongo)+243 Congo (Republic) (Congo-Brazzaville)+242 Cook Islands+682 Costa Rica+506 Côte d’Ivoire+225 Croatia (Hrvatska)+385 Cuba+53 Curaçao+599 Cyprus (Κύπρος)+357 Czech Republic (Česká republika)+420 Denmark (Danmark)+45 Djibouti+253 Dominica+1 Dominican Republic (República Dominicana)+1 Ecuador+593 Egypt (‫مصر‬‎)+20 El Salvador+503 Equatorial Guinea (Guinea Ecuatorial)+240 Eritrea+291 Estonia (Eesti)+372 Ethiopia+251 Falkland Islands (Islas Malvinas)+500 Faroe Islands (Føroyar)+298 Fiji+679 Finland (Suomi)+358 France+33 French Guiana (Guyane française)+594 French Polynesia (Polynésie française)+689 Gabon+241 Gambia+220 Georgia (საქართველო)+995 Germany (Deutschland)+49 Ghana (Gaana)+233 Gibraltar+350 Greece (Ελλάδα)+30 Greenland (Kalaallit Nunaat)+299 Grenada+1 Guadeloupe+590 Guam+1 Guatemala+502 Guernsey+44 Guinea (Guinée)+224 Guinea-Bissau (Guiné Bissau)+245 Guyana+592 Haiti+509 Honduras+504 Hong Kong (香港)+852 Hungary (Magyarország)+36 Iceland (Ísland)+354 India (भारत)+91 Indonesia+62 Iran (‫ایران‬‎)+98 Iraq (‫العراق‬‎)+964 Ireland+353 Isle of Man+44 Israel (‫ישראל‬‎)+972 Italy (Italia)+39 Jamaica+1 Japan (日本)+81 Jersey+44 Jordan (‫الأردن‬‎)+962 Kazakhstan (Казахстан)+7 Kenya+254 Kiribati+686 Kosovo+383 Kuwait (‫الكويت‬‎)+965 Kyrgyzstan (Кыргызстан)+996 Laos (ລາວ)+856 Latvia (Latvija)+371 Lebanon (‫لبنان‬‎)+961 Lesotho+266 Liberia+231 Libya (‫ليبيا‬‎)+218 Liechtenstein+423 Lithuania (Lietuva)+370 Luxembourg+352 Macau (澳門)+853 Macedonia (FYROM) (Македонија)+389 Madagascar (Madagasikara)+261 Malawi+265 Malaysia+60 Maldives+960 Mali+223 Malta+356 Marshall Islands+692 Martinique+596 Mauritania (‫موريتانيا‬‎)+222 Mauritius (Moris)+230 Mayotte+262 Mexico (México)+52 Micronesia+691 Moldova (Republica Moldova)+373 Monaco+377 Mongolia (Монгол)+976 Montenegro (Crna Gora)+382 Montserrat+1 Morocco (‫المغرب‬‎)+212 Mozambique (Moçambique)+258 Myanmar (Burma) (မြန်မာ)+95 Namibia (Namibië)+264 Nauru+674 Nepal (नेपाल)+977 Netherlands (Nederland)+31 New Caledonia (Nouvelle-Calédonie)+687 New Zealand+64 Nicaragua+505 Niger (Nijar)+227 Nigeria+234 Niue+683 Norfolk Island+672 North Korea (조선 민주주의 인민 공화국)+850 Northern Mariana Islands+1 Norway (Norge)+47 Oman (‫عُمان‬‎)+968 Pakistan (‫پاکستان‬‎)+92 Palau+680 Palestine (‫فلسطين‬‎)+970 Panama (Panamá)+507 Papua New Guinea+675 Paraguay+595 Peru (Perú)+51 Philippines+63 Poland (Polska)+48 Portugal+351 Puerto Rico+1 Qatar (‫قطر‬‎)+974 Réunion (La Réunion)+262 Romania (România)+40 Russia (Россия)+7 Rwanda+250 Saint Barthélemy+590 Saint Helena+290 Saint Kitts and Nevis+1 Saint Lucia+1 Saint Martin (Saint-Martin (partie française))+590 Saint Pierre and Miquelon (Saint-Pierre-et-Miquelon)+508 Saint Vincent and the Grenadines+1 Samoa+685 San Marino+378 São Tomé and Príncipe (São Tomé e Príncipe)+239 Saudi Arabia (‫المملكة العربية السعودية‬‎)+966 Senegal (Sénégal)+221 Serbia (Србија)+381 Seychelles+248 Sierra Leone+232 Singapore+65 Sint Maarten+1 Slovakia (Slovensko)+421 Slovenia (Slovenija)+386 Solomon Islands+677 Somalia (Soomaaliya)+252 South Africa+27 South Korea (대한민국)+82 South Sudan (‫جنوب السودان‬‎)+211 Spain (España)+34 Sri Lanka (ශ්‍රී ලංකාව)+94 Sudan (‫السودان‬‎)+249 Suriname+597 Svalbard and Jan Mayen+47 Swaziland+268 Sweden (Sverige)+46 Switzerland (Schweiz)+41 Syria (‫سوريا‬‎)+963 Taiwan (台灣)+886 Tajikistan+992 Tanzania+255 Thailand (ไทย)+66 Timor-Leste+670 Togo+228 Tokelau+690 Tonga+676 Trinidad and Tobago+1 Tunisia (‫تونس‬‎)+216 Turkey (Türkiye)+90 Turkmenistan+993 Turks and Caicos Islands+1 Tuvalu+688 U.S. Virgin Islands+1 Uganda+256 Ukraine (Україна)+380 United Arab Emirates (‫الإمارات العربية المتحدة‬‎)+971 United Kingdom+44 United States+1 Uruguay+598 Uzbekistan (Oʻzbekiston)+998 Vanuatu+678 Vatican City (Città del Vaticano)+39 Venezuela+58 Vietnam (Việt Nam)+84 Wallis and Futuna (Wallis-et-Futuna)+681 Western Sahara (‫الصحراء الغربية‬‎)+212 Yemen (‫اليمن‬‎)+967 Zambia+260 Zimbabwe+263 Åland Islands+358 A valid phone number is required. Comments* Attach Resume* No file chosen Browse

The role involves managing and analyzing complex clinical datasets for a TAVR trial to ensure data integrity and regulatory compliance. Key tasks include developing trial datasets, performing quality checks, and generating submission-ready reports for FDA/EMA.

Candidates need an advanced degree in Data Science or a related field with experience in clinical trial data management, specifically within cardiology or medical devices. Proficiency in SAS, R, Python, and CDISC standards is required along with the ability to work onsite full-time.

• 401(k) • Dental insurance • Vision insurance • Disability insurance • Employee assistance program • Flexible spending account • Health Savings Account • Health insurance • Life insurance • Paid time off • Relocation assistance • Stock options

• Visualisation de donnéesSouhaitée
• Power BISouhaitée
• SQLSouhaitée
• TableauSouhaitée
• Google CloudSouhaitée
• PythonSouhaitée

Relevées dans la description du poste. Confirmez les exigences importantes ci-dessus.

• Clinical Trial Data Management
• SAS
• R
• Python
• SQL
• Oracle
• Medidata
• REDCap
• CDISC Standards
• SDTM
• ADaM
• Tableau
• Power BI
• Data Visualization
• GCP
• Regulatory Compliance

• Data & Analytics
• Healthcare
• Science & Research
• Technology
• Engineering

Formation minimale

Maîtrise

Expérience minimale

2+ ans

Postuler avant le

6 sept. 2026

Langue de l’offre

anglais

Heures de travail

40 heures par semaine

Niveau d’expérience

Entry level