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Principal Biostatistician

extra holidays - extra parental leave - fully flexible
Remote: 
Full Remote
Experience: 
Senior (5-10 years)
Work from: 
India

Offer summary

Qualifications:

PhD or MS in Statistics or related discipline, 3+ years (PhD) or 5+ years (MS) experience, Proficient in SAS programming, Competent in written and oral English.

Key responsabilities:

  • Lead project teams to completion
  • Interact with clients on statistical issues
Parexel logo
Parexel XLarge http://www.parexel.com/
10001 Employees
About Parexel
Parexel is among the world’s largest clinical research organizations (CROs), providing the full range of Phase I to IV clinical development services to help life-saving treatments reach patients faster. Leveraging the breadth of our clinical, regulatory and therapeutic expertise, our team of more than 21,000 global professionals collaborates with biopharmaceutical leaders, emerging innovators and sites to design and deliver clinical trials with patients in mind, increasing access and participation to make clinical research a care option for anyone, anywhere. Our depth of industry knowledge and strong track record gained over the past 40 years is moving the industry forward and advancing clinical research in healthcare’s most complex areas, while our innovation ecosystem offers the best solutions to make every phase of the clinical trial process more efficient. With the people, insight and focus on operational excellence, we work With HeartTM every day to treat patients with dignity and continuously learn from their experiences, so every trial makes a difference. For more information, visit parexel.com. Community Guidelines Because Parexel’s social media channels are open to the general public and employees, we are not responsible for views expressed other than our own. However, we do not tolerate posts that are: • Abusive, harassing or threatening to others. • Defamatory, offensive, obscene, vulgar or depicting violence. • Hateful targeting by race/ethnicity, age, color, creed, religion, gender, sexual preference or orientation, nationality or political beliefs. • Sexually explicit or pornographic. • Fraudulent, deceptive, libelous, misleading or unlawful. • Referencing criminal or illegal activity. • Spamming. We reserve the right to remove any comments that do not adhere to our guidelines as well as report users who violate the rules of our page.
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Job description

When our values align, there's no limit to what we can achieve.
 
At Parexel, we all share the same goal - to improve the world's health. From clinical trials to regulatory, consulting, and market access, every clinical development solution we provide is underpinned by something special - a deep conviction in what we do.

Each of us, no matter what we do at Parexel, contributes to the development of a therapy that ultimately will benefit a patient. We take our work personally, we do it with empathy and we're committed to making a difference.

Key Accountabilities:

  • Coordinate and lead a project team to successful completion of a project within given timelines and budget.
  • Interact with clients as key contact with regard to statistical and contractual issues
  • Perform QC of derived datasets, tables, figures and data listings produced by other members of the department.
  • Check own work in an ongoing way to ensure first-time quality.
  • Understand and apply advanced statistical methods.
  • Lead production and quality control of randomizations, analysis plans, statistical reports, statistical sections of integrated clinical reports and other process supporting documents.
  • Provide a supporting role as a non-voting independent statistician providing data and analysis for DMC review.
  • Support of Business Development, e.g. by actively contributing to study design considerations in internal and client meetings, providing and discussing sample size scenarios, support of budget and proposal development, attending and preparing bid defense meetings
  • Travel to, attend and actively contribute to all kind of client meetings as appropriate (e.g. discussing analysis concepts, presenting and discussing study results)
  • Additional responsibilities as defined by supervisor/manager.

Skills:

  • Good analytical skills
  • Good project management skills
  • Professional attitude
  • Attention to detail
  • Thorough understanding of statistical issues in clinical trials
  • Prior experience with SAS programming required
  • Ability to work independently
  • Good leadership skills
  • Good business awareness/ business development skills
  • Willingness to work in a matrix environment and to value the importance of teamwork.

Knowledge and Experience:

  • PhD in Statistics or related discipline with 3+years of experience or MS in Statistics or related discipline with 5+ years of experience
  •  Competent in written and oral English in addition to local language

 Education: · PhD in Statistics or related discipline, MS in Statistics or related discipline

#reexcel

Required profile

Experience

Level of experience: Senior (5-10 years)
Industry :
Pharmaceuticals
Spoken language(s):
English
Check out the description to know which languages are mandatory.

Hard Skills

Statistical MethodsProject ManagementSAS MacrosBusiness Development

Other Skills

  • Professionalism
Are you interested?

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