- Global healthcare leader uniting caring with discovery to make life better for people worldwide.
- Strong focus on innovation integrity and inclusion fostering a people-first culture.
- Opportunity to impact millions of lives through breakthrough medicines and research.
- Commitment to employee growth and development with continuous learning and career advancement.
If thats you lets talk! |
| Job Type : Full Time |
| Location : Indianapolis Indiana |
| Pay : Great Pay! |
| Job Description |
What you will be doing: - Develop or assist in the development of protocol designs clinical plans and data analysis plans in collaboration with physicians and clinical research scientists.
- Provide input on study protocol design studies and write protocols for the conduct of each study.
- Select statistical methods for data analysis and author the corresponding sections of the protocol and statistical analysis plan.
- Conduct data analysis once a reporting database is created.
- Collaborate with data sciences in the planning and implementation of data quality assurance plans.
- Maintain proficiency in applying new and varied statistical methodologies.
- Perform peer review of work products from other statistical colleagues.
- Collaborate with team members to write reports and communicate study results.
- Assist or be responsible for communicating study results via regulatory submissions manuscripts or oral presentations.
- Understand disease states competitive landscapes and the regulatory environment to enhance customer focus and collaboration.
- Perform work in full compliance with assigned curriculum and follow applicable corporate medical local and departmental policies.
- Introduce and apply innovative methodology and tools to solve critical problems.
- Lead projects independently and apply technical expertise to influence business decisions.
Experience you will need: - Ph.D. in Statistics or Biostatistics with at least 3 years of experience in Clinical Research and Development.
- Proficient in statistical programming languages/software such as SAS R Spotfire WinBUGs etc.
- Interpersonal communication skills for effective customer consultation.
- Teamwork and leadership skills.
- Technical expertise and application with working knowledge of experimental design and statistical analysis.
- Self-management skills with a focus on results for timely and accurate completion of competing deliverables.
- Resource management skills.
- Creativity and innovation.
- Demonstrated problem-solving ability and critical thinking.
|
| Our client asked me to submit 3 great people within the next few days. We work directly with the hiring manager and can arrange interviews within a few days |
#INDEH123
Global healthcare leader uniting caring with discovery to make life better for people worldwide. Strong focus on innovation integrity and inclusion fostering a people-first culture. Opportunity to impact millions of lives through breakthrough medicines and research. Commitment to employee growt...
- Global healthcare leader uniting caring with discovery to make life better for people worldwide.
- Strong focus on innovation integrity and inclusion fostering a people-first culture.
- Opportunity to impact millions of lives through breakthrough medicines and research.
- Commitment to employee growth and development with continuous learning and career advancement.
If thats you lets talk! |
| Job Type : Full Time |
| Location : Indianapolis Indiana |
| Pay : Great Pay! |
| Job Description |
What you will be doing: - Develop or assist in the development of protocol designs clinical plans and data analysis plans in collaboration with physicians and clinical research scientists.
- Provide input on study protocol design studies and write protocols for the conduct of each study.
- Select statistical methods for data analysis and author the corresponding sections of the protocol and statistical analysis plan.
- Conduct data analysis once a reporting database is created.
- Collaborate with data sciences in the planning and implementation of data quality assurance plans.
- Maintain proficiency in applying new and varied statistical methodologies.
- Perform peer review of work products from other statistical colleagues.
- Collaborate with team members to write reports and communicate study results.
- Assist or be responsible for communicating study results via regulatory submissions manuscripts or oral presentations.
- Understand disease states competitive landscapes and the regulatory environment to enhance customer focus and collaboration.
- Perform work in full compliance with assigned curriculum and follow applicable corporate medical local and departmental policies.
- Introduce and apply innovative methodology and tools to solve critical problems.
- Lead projects independently and apply technical expertise to influence business decisions.
Experience you will need: - Ph.D. in Statistics or Biostatistics with at least 3 years of experience in Clinical Research and Development.
- Proficient in statistical programming languages/software such as SAS R Spotfire WinBUGs etc.
- Interpersonal communication skills for effective customer consultation.
- Teamwork and leadership skills.
- Technical expertise and application with working knowledge of experimental design and statistical analysis.
- Self-management skills with a focus on results for timely and accurate completion of competing deliverables.
- Resource management skills.
- Creativity and innovation.
- Demonstrated problem-solving ability and critical thinking.
|
| Our client asked me to submit 3 great people within the next few days. We work directly with the hiring manager and can arrange interviews within a few days |
#INDEH123
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Job Location:
Yearly Salary:
$ 160000 - 250000
Posted on:
30+ days ago
Vacancies:
1 Vacancy
