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FSP Principal Biostatistician for Early Phase Clinical (PK)

ダーラム, ノースカロライナ州 Full time R1441283

ダーラム, ノースカロライナ州| ノースカロライナ州| Remote

  • Full Time
  • Level: Entry-level, Mid-level, Senior-level

Build a rewarding career in life sciences consulting and forge your own path. Partner with collaborative teams and leaders across unique projects and geographies, delivering innovative solutions to the most complex healthcare problems along the way. Working at IQVIA means changing outcomes for patients one data set, product offering and innovative solution at a time.

As a Consultant at IQVIA, you'll have the opportunity to grow your career and explore opportunities in brand and integrated research solutions, go-to-market strategy, commercial excellence, real world data, financial investor consulting and more.

応募

Success Profile

IQVIAで活躍しているコンサルタントは? 共通するスキル・マインドセットはこちらです。

  • ACHIEVER
  • COMMUNICATION
  • CRITICAL-THINKER
  • ADAPTABLE
  • STRATEGIC
  • DETAIL-ORIENTED

What you can expect

Professional Development

スキル向上できる環境

Highly Specialized

専門分野に特化した働き方

Growth Potential

ステップアップに向けた明確なキャリアパス

Collaboration

共通の目標に向かって、協力し合うチーム

Innovative Projects

複雑な課題を革新的な方法で解決

Best-in-Class Training

知識とスキルを向上するためのトレーニング

大学卒業後、IQVIAに入社し、4年間で素晴らしい経験を積めました。自身のマネージャーはプロフェッショナルとパーソナルな面で成長を促してくれました

Arthur

コンサルタント

FSP Principal Biostatistician for Early Phase Clinical (PK)

ダーラム, ノースカロライナ州, アメリカ合衆国| ノースカロライナ州, アメリカ合衆国| Remote R1441283
応募

Job Description

Job Level: FSP Principal Biostatistician for Early Phase Clinical (PK)

Location: Home-based in the U.S. or Canada

Why DSSS?

Data Sciences Staffing Solutions, DS3, is a unit within IQVIA that provides our sponsors with fully embedded resources through a Functional Service Provider (FSP) partnership. This means you get all the benefits of working for an industry leading global CRO while collaborating with  a sponsor teams and utilizing sponsor systems. These sponsor clients include world class pharmaceutical and biotech companies offering you unique opportunities to influence the future of medicine and advance therapies.

Job Summary:

The Principal Biostatistician is responsible for providing statistical support for drug development programs in early phases of development, focusing on healthy normal studies with PK and PD endpoints.

Additional Benefits:

  • Home-based remote working opportunities
  • Work/life balance as well as flexible schedules
  • Collaborating with motivated, high-performance, statistical and research teams
  • Technical training and tailored development curriculum
  • Research opportunities that match your unique skillset
  • Promising career trajectory
  • Job stability: long-term engagements and re-deployment opportunities
  • Focus on bringing new therapies to market rather than project budgets and change orders.
  • Experience with regulatory submissions
  • Engaging, fast-paced environment
  • Good work-life balance

Job Requirements:

  • Collaborate with multidisciplinary project teams to establish project timelines.
  • Provide statistical input to study protocols.
  • Writes the statistical sections of clinical trial protocols, while consulting with internal and external experts.
  • Write or review statistical analysis plans.
  • Monitor internal and CRO project activities including timelines, deliverables, and availability of resources.
  • Collaborates with Data Management, Clinical Development, and Clinical Operations with statistical expertise.
  • Contributes to clinical study reports and other regulatory documents e.g., DSURs, Briefing Documents, etc.
  • Provide guidance and supervision to programmers in authoring of analysis dataset specifications and programming of tables, listings, and figures.
  • Interpret study results and review reports of study results for accuracy.
  • Participate and contribute to authoring of Clinical Development Plan.
  • Support exploratory analyses and medical affairs publications.
  • Participate in pre-IND and NDA activities.
  • Participates in other activities and meetings to support Biostatistics and the Development Team as needed.
  • Demonstrated ability to work independently in project management and decision making.
  • Able to effectively communicate statistical concepts to colleagues
  • Able to effectively manage CROs.
  • Ability to use SAS and/or R to perform efficacy analyses and validate important data derivations when necessary.
  • Understanding of ICH GCP as well as general knowledge of industry practices and standards. Experience with CDISC, including SDTM, ADaM, CDASH.

Qualifications (Minimal acceptable level of education, work experience, and competency)

  • PhD in Statistics, Biostatistics, or related field with 5+ years industry experience.
  • MS in Statistics, Biostatistics, or related field with 7+ years of industry experience.
  • 3 years of experience in statistical analysis of PK and PD endpoints.

Desired Experience:

  • Familiarity with R programming language and other statistical software, including EAST.
  • Experience with dermatology or immunology.
  • Knowledge of simulations, multivariate analyses, and biomarker analyse.

#LI-Remote

#LI-NITINMAHAJAN

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com

We are committed to providing equal employment opportunities for all, including veterans and candidates with disabilities. https://jobs.iqvia.com/eoe

IQVIA’s ability to operate and provide certain services to customers and partners necessitates IQVIA and its employees meet specific requirements regarding COVID-19 vaccination status.https://jobs.iqvia.com/covid-19-vaccine-status

The potential base pay range for this role, when annualized, is $131,300.00 - $243,900.00. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.
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