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Biorasi, LLC

Related companies:

🏢 Nuvalent, Inc.
🏢 Praxis Precision Medicines, Inc.
🏢 ClinChoice

Jobs at this company:

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🔥 Proposal Developer
Posted 2024-10-26

đź“Ť USA

🔍 Clinical research

  • Minimum Bachelor's Degree; degree in a life science preferred but not required.
  • 1-2 years of experience in Proposal Development for CRO/pharmaceutical industry.
  • Computer literacy with proficiency in Microsoft Office Suite, especially PowerPoint.
  • Proficiency in Salesforce.
  • Excellent verbal and communication skills.

  • Support Business Development lead with proposal building and vendor quotes.
  • Assist with completion of all Sponsor Requests for Information and maintain RFI library.
  • Schedule and participate in Sponsor introductory and ongoing calls.
  • Engage in internal strategy discussions related to assigned Sponsor projects.
  • Research and collect data pertinent to assigned Sponsor projects.
  • Create presentations and visuals to support assigned Sponsor projects.
  • Collaborate with internal teams for information gathering and updates.
  • Support scheduling for Bid Defense sessions and attend prep sessions.

Business DevelopmentSalesforceStrategyBusiness developmentCommunication SkillsMicrosoft Office Suite

Posted 2024-10-26
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🔥 Senior Associate, Statistical Programming
Posted 2024-10-18

đź“Ť India

🔍 Clinical research

  • Bachelor’s Degree in Mathematics/Statistics, Life Sciences, Computer Science, or related field.
  • Fluent English (oral and written).
  • At least 2 years’ experience in Biostatistics or Statistical Programming within the pharmaceutical industry.
  • Experience in planning and coordinating programming activities and leading programming teams is strongly preferred.
  • Ability to multitask and prioritize work, paying close attention to detail, timeliness and quality.
  • Strong problem-solving and leadership skills.
  • Excellent team working characteristics for cross-functional teams.
  • Significant knowledge of drug development and clinical research.
  • Good knowledge of ICH GCP and worldwide applicable regulatory requirements.
  • Ability to operate in a fast-paced environment.
  • Excellent time management and planning skills.
  • Excellent communication skills, both written and verbal.

  • Create outputs that meet quality standards and project requirements.
  • Maintain well organized, complete up-to-date project documentation, and verification/quality control documents.
  • Read and understand the Study documents and provide feedback.
  • Contribute to project-specific objectives and team deliverables.
  • Responsible for on-time delivery across concurrent programming deliverables.
  • Develop annotated CRFs and regulatory submission documentation.
  • Develop programming specifications and support clinical study reports.
  • Develop/validate CDISC compliant datasets and TLFs.
  • Maintain a high level of professionalism and quality.
  • Undergo Regulatory trainings and other statistical programming duties.

LeadershipCommunication SkillsAnalytical SkillsCollaboration

Posted 2024-10-18
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🔥 Lead, Statistical Programming
Posted 2024-10-18

đź“Ť India

🔍 Clinical research

  • Bachelor’s Degree in Mathematics/Statistics, Life Sciences, Computer Science or related field.
  • At least 3 years' experience in Biostatistics or Statistical Programming.
  • Experience in planning and coordinating programming activities.
  • Strong problem-solving and leadership skills.
  • Excellent communication skills, both written and verbal.
  • Significant knowledge of drug development and clinical research.
  • Good knowledge of ICH GCP and worldwide regulatory requirements.
  • Ability to multitask and prioritize work.

  • Ensure that outputs meet quality standards and project requirements.
  • Guide and ensure well organized, complete up-to-date project documentation.
  • Develop and maintain standard programs, macros, templates, and libraries.
  • Contribute to project-specific objectives and team deliverables.
  • Responsible for on-time delivery of concurrent programming deliverables.
  • Resolve complex statistical programming obstacles and provide guidance.
  • Develop annotated CRFs and regulatory submission documentation.
  • Develop programming specifications compliant with CDISC standards.
  • Develop/validate CDISC compliant datasets and TLFs.
  • Serve as a back-up for sponsors and project team for programming activities.
  • Review/approve electronic Case Report Forms as required.
  • Drive small teams of programmers in programming activities.
  • Maintain professionalism, performance, and quality.

LeadershipCross-functional Team LeadershipCommunication SkillsAnalytical SkillsCollaborationProblem SolvingAttention to detail

Posted 2024-10-18
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