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Innovaderm Research Inc.
Innovaderm Research Inc.
201 – 500 Darbuotojai
Farmacijos produktaiKonsultavimasSveikatos priežiūra
Innovaderm Research Inc. yra į dermatologiją orientuota klinikinių tyrimų sutarčių tyrimų organizacija (CRO), remianti klinikinį vystymą nuo I iki IV fazės. Nuo 2000 m. įmonė bendradarbiauja su farmacijos ir sveikatos priežiūros organizacijomis Šiaurės Amerikoje ir Europoje, teikdama dermatologijos tyrimų planavimo, reguliavimo konsultacijų, projektų valdymo, pacientų pritraukimo ir duomenų valdymo paslaugas.
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Darbai įmonėje

Remote Project Director, Dermatology and Rheumatology

Lead multinational dermatology and rheumatology clinical study portfolios at Indero, overseeing project managers, budgets, regulatory compliance, and client delivery.

USJungtinės ValstijosNCŠiaurės KarolinaNuotolinisVisas etatasVadovasPrivaloma Kalba: anglųDirektorius
PMP

Aprašymas

  • Direct a portfolio of clinical studies and the project managers responsible for delivering them.
  • Ensure studies meet therapeutic-area and client requirements.
  • Represent the company to customers and sustain client satisfaction.
  • Communicate program deliverables clearly and effectively.
  • Keep studies aligned with quality standards, SOPs, GCP, ICH guidelines, and applicable regulations.
  • Oversee executed contracts and study finances, including budgets and expenses.
  • Track and assess project progress with timelines and analytical tracking tools.
  • Build and maintain detailed knowledge of the assigned portfolio’s therapeutic areas and clients.
  • Apply lessons from individual studies across assigned studies and client engagements.
  • Lead contingency planning and risk-reduction efforts.
  • Contribute operational expertise and strategy to proposal development and pricing.
  • Advance performance, operational efficiency, and innovative approaches.
  • Provide line-management oversight and support project management leadership as an operational and therapeutic-area expert.

Reikalavimai

  • Bachelor of Science degree in a relevant field.
  • At least 15 years of industry experience.
  • At least 5 years of experience at a CRO.
  • At least 10 years managing clinical projects, covering every phase from start-up through closeout, functional services, and vendors.
  • Experience with mid-size and large studies spanning more than 10–15 countries across multiple regions (North America, South America, APAC, MENA, and Europe) is preferred.
  • Experience leading concurrent, multicenter, multinational Phase III trials, including project budget tracking and forecasting.
  • Extensive experience supervising, mentoring, and coaching project managers.
  • Substantial business development experience, such as preparing proposals, presenting to clients, and participating in bid-defense meetings.
  • Experience mentoring and coaching a representative number of project managers.
  • Dermatology or rheumatology experience is required.
  • Strong knowledge of Good Clinical Practice.
  • Knowledge of applicable Health Canada and U.S. Food and Drug Administration regulations and guidelines.
  • PMP or PRINCE2 certification is an asset.
  • A master’s degree is an asset.

Privalumai

  • Flexible work schedule.
  • Home-based position.
  • Ongoing learning and development.
  • 401(k) plan.
  • Benefits package.
  • Bonus plan.
  • Career advancement opportunities.

Susiję darbai

Medtronic

Director of Clinical Research, Peripheral Nerve Stimulation

Medtronic
H1B vizos rėmėjasGamybaSveikatos draudimasSveikatos priežiūra
USJungtinės ValstijosMNMinesotaOHOhajas
212 800 $ – 319 200 $ / metai
Darbas vietojeVisas etatasVadovasPrivaloma Kalba: anglųKlinikiniai tyrimai
Google Cloud Platform

Lead Medtronic’s global clinical evidence strategy for peripheral nerve stimulation therapies throughout the product lifecycle. Oversee premarket and postmarket research supporting scientific, regulatory, reimbursement, and commercial goals.

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IQVIA

Clinical Research Associate, Sponsor Dedicated

IQVIA
H1B vizos rėmėjasGamybaKonsultavimasRinkodara
USJungtinės ValstijosFLFloridaKSKanzasasNJNaujasis DžersisNCŠiaurės KarolinaUTJuta
74 500 $ – 197 500 $ / metai
Darbas vietojeVisas etatasJaunesnysis specialistasVidutinis lygisDiplomas nebūtinasPrivaloma Kalba: anglųKlinikiniai tyrimai
Google Cloud Platform

Monitor clinical trial sites and support protocol compliance, patient recruitment, and study documentation for IQVIA. Coordinate with site staff and project teams to help trials meet quality standards and milestones.

Atidaryti
Regeneron

Clinical Study Specialist at Regeneron

Regeneron
H1B vizos rėmėjasBiotechnologijaGamybaSveikatos priežiūra
USJungtinės ValstijosMAMasačusetsasNJNaujasis DžersisNYNiujorkas
93 900 $ – 153 300 $ / metai
HibridinisVisas etatasJaunesnysis specialistasVidutinis lygisPrivaloma Kalba: anglųBendraKlinikinis specialistas
Google Cloud Platform

Support Regeneron clinical trial teams by coordinating study data, sites, reporting, and close-out activities. Help keep studies on track from site activation through completion.

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