Salesforce Developer

CareerCircle
San Francisco, United States of America
2 days ago

Role details

Contract type
Permanent contract
Employment type
Full-time (> 32 hours)
Working hours
Regular working hours
Languages
English
Experience level
Senior
Compensation
$ 300K

Job location

San Francisco, United States of America

Tech stack

Agile Methodologies
Artificial Intelligence
Data analysis
CSS
Clinical Data Management
Computer Programming
Data Validation
Digital Data
R
Machine Learning
Requirements Management
SAS (Software)
Tableau
Data Management

Job description

Marketing Leadership Management Innovation Statistics Compassion Epidemiology Data Science Biostatistics Randomization SAS (Software) Clinical Trials Risk Management Data Management Telephone Skills Decision Science Project Management Influencing Skills Strategic Planning Numerical Analysis Statistical Methods Evaluation Strategy Infectious Diseases Vaccine Development Statistical Analysis Contingent Workforce Strategic Management Statistical Software Clinical Study Design Regulatory Requirements Research And Development R (Programming Language) Product Lifecycle Management Non-Disclosure Agreement (Intellectual Property Law), In BARDS (Biostatistics and Research Decision Sciences), a distinguished department within our company's renowned Research and Development division, quantitative scientists, in partnership with other subject matter experts, apply state-of-the art scientific methodologies and tools to enable the discovery, development, regulatory approval, manufacturing, and marketing of medical drugs and vaccines for the benefit of patients and global human health., * Serve as the CSS therapeutic area lead for the vaccine and infectious disease (VID) projects.

  • Provide statistical leadership and support to the Risk Management and Safety Teams (RMSTs) in the strategic planning and execution of compound level safety evaluation across product life cycle in vaccine and drug programs
  • Design, develop and implement innovative statistical methods and tools for safety evaluation.

Primary Activities:

  • Provide statistical leadership for compound safety evaluation strategy and analysis in vaccines and infectious diseases; support CSS projects in other therapeutic areas as needed.
  • Partner with Clinical Safety Risk Management, Early/Late Development Statistics, Epidemiology, Programming, and other RMST functions to plan and execute on aggregate safety evaluation in vaccine and drug projects
  • Ensure safety deliverables meet analysis requirements, relevant SOPs and regulatory guidance.
  • Communicate safety-analysis results and recommendations to teams, management, regulators, and investigators.
  • Develop processes, job aids, statistical methods, and tools for safety evaluation that address scientific and business needs, Planning Marketing Templates Annuities Operations Leadership Governance Wholesaling Fundraising Coordinating Prioritization Tax Accounting Decision Making Social Security Data Validation Virtual Training Financial Analysis Project Management Financial Tracking Portfolio Management Investment Decisions Investment Performance Artificial Intelligence Employment Applications Employee Assistance Programs Health And Wellness Coaching Tableau (Business Intelligence Software) +0

Requirements

  • PhD or equivalent degree in statistics/biostatistics or related discipline with a minimum of 6 years relevant work experience, or master's with a minimum of 9 years relevant work experience., * Solid knowledge of statistical analysis methodologies. Solid experience of using statistical software (eg SAS or R).
  • Solid knowledge of regulatory requirements regarding the analysis and reporting of safety data.
  • Strong project management and leadership skills, including the ability to influence cross-functional teams and align priorities at the Therapeutic Area level.
  • Knowledge of and experience with clinical trial design and analysis. Experience with the analysis and interpretation of integrated safety data
  • Knowledge of statistical methods appropriate for the analysis of clinical trial data in both randomized and non-randomized studies

Preferred:

  • Solid Knowledge of drug/vaccine development process from discovery, preclinical research, clinical trials (Phase 1, 2 and 3), NDA review to post-marketing evaluation
  • Knowledge and experience in developing/applying AI tools in drug and vaccine development projects., Biostatistics, Clinical Risk Management, Clinical Study Design, Clinical Trials, Clinical Trials Analysis, Data Management, Data Science, Numerical Analysis, Safety Management, Statistical Analysis, Statistical Software, Strategic Management, Strategic Planning, Leadership Management Innovation Compassion Digital Data Adaptability Communication Data Analysis Collaboration Pharmaceuticals Detail Oriented Risk Mitigation Market Research Decision Making Customer Service Brand Management Telephone Skills Agile Methodology Vendor Management Growth Mindedness Marketing Budgets Project Management Influencing Skills Strategic Thinking Operationalization Pharmacy Operations Medical Prescription Contingent Workforce Business Intelligence Market Access Strategy Strategic Prioritization Influencing Without Authority Cross-Functional Collaboration Customer Relationship Management Tableau (Business Intelligence Software), Leadership Management Automation Governance Innovation Compassion Scalability Supply Chain Data Science Communication User Feedback Accountability Prioritization Responsible AI Pharmaceuticals Design Thinking Product Strategy Product Roadmaps Machine Learning Telephone Skills Agile Methodology Change Management Lean Manufacturing Value Propositions Product Management Business Valuation Cycle Time Variation User Experience (UX) Contingent Workforce Regulatory Compliance Emerging Technologies Solution Architecture Waterfall Methodology Stakeholder Management Stakeholder Engagement Artificial Intelligence Relationship Management Requirements Management Stakeholder Communications User Experience (UX) Design Product Lifecycle Management Project Portfolio Management Operational Acceptance Testing Customer Relationship Management +0

Google Project Management

Benefits & conditions

We are proud to be a company that embraces the value of bringing together, talented, and committed people with diverse experiences, perspectives, skills and backgrounds. The fastest way to breakthrough innovation is when people with diverse ideas, broad experiences, backgrounds, and skills come together in an inclusive environment. We encourage our colleagues to respectfully challenge one another's thinking and approach problems collectively.

Learn more about your rights, including under California, Colorado and other US State Acts

The salary range for this role is $190,800.00 - $300,300.00

About the company

Merck & Co., Inc., Rahway, NJ, USA, also known as Merck Sharp & Dohme LLC, Rahway, NJ, USA, does not accept unsolicited assistance from search firms for employment opportunities. All CVs / resumes submitted by search firms to any employee at our company without a valid written search agreement in place for this position will be deemed the sole property of our company. No fee will be paid in the event a candidate is hired by our company as a result of an agency referral where no pre-existing agreement is in place. Where agency agreements are in place, introductions are position specific. Please, no phone calls or emails.

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