Financial Services in Dickinson, Michigan | Fast Recruitment & Job Search

This position will work cross functionally to define business requirements for data governance and ad hoc data reporting

Software Engineering experience with proficiency in at least one high-level programming language (preferably Python).

Knowledge of data visualization tools (e.g. Tableau)

Experience with AWS Data Lakes, S3, Redshift

Key Responsibilities will include, but are not limited to the following:

This position will focus on building scalable ETL data pipelines that facilitate data warehousing for clinical trial and operational data

Learn and understand the basic knowledge of clinical trial, Database design.

Provide SAS, Spotfire coding skill to real time safety data visualization. And understand, possibly modify IronPython, R in templates.

Experience on visualization software such as Spotfire, Tableau, R Shinny etc. is a plus

Experience on Clinical trial data is a plus

Knowledge of SAS, Spotfire, IronPython, R

Key Responsibilities will include, but are not limited to the following:

Strong organizational, time-management, interpersonal and communication capabilities

Develop knowledge of other roles and functions within Real-World Evidence and cross-functional team.

Learn the ability to handle multiple tasks, maintain clear tracking and documentation, and manage tight project timelines

Must have a good working knowledge of SAS, STATA, SQL, or R

Experience with secondary data analysis, including electronic medical record and/or medical claims databases

Demonstrated experience with observational research

Tracking and coordinating successful implementation of short and long-term, cross-functional workstreams under the guidance of the manager

Employing research and business acumen, strategic thinking, and analytical skills to conceptualize high value initiatives for the research organization

Superior problem-solving skills and ability to work well under pressure in a demanding environment

Excellent verbal and written communication skills; strong presentation skills

High level of agility; eager to develop new skills and areas of expertise

Key Responsibilities will include, but are not limited to the following:

Strong relationship management skills with internal stakeholders and external contacts and resources.

Excellent task management skills (specifically project planning, prioritization, objective setting, meeting management and plan execution) are required.

Manage third party agencies/projects to source relevant CI

Knowledge regarding the drug development and commercialization process in order to assess and contextualize competitive efforts.

Experience in use of online data sources and scientific/market databases (e.g., Pubmed, clinicaltrials.gov, TrialTrove, Evaluate Pharma , etc.)

History of effective written communication skills (including both PowerPoint and Word/email mediums).

Demonstrate good verbal communication skills and interpersonal skills.

Key Responsibilities will include, but are not limited to the following:

Under general supervision, performs experiments that support activities in Analytical Development and Operations.

Operates scientific equipment, selects appropriate methods and techniques to perform experiments, and prepares related reports.

Plans and organizes details of experiments with guidance.

Uses established data, reports, and previous results to identify inappropriate variances and concerns and discusses inconsistent results with supervisor.

This position will work cross functionally to define business requirements, design the supporting cloud (AWS) architecture and execute building the services.

Key Responsibilities will include, but are not limited to the following:

Showcase your work with a final poster board presentation near the conclusion of your internship

Must be at least 18 years old

Must have a minimum GPA of 2.8

Authorized to work in the United States without Sponsorship now or in the future or CPT/OPT through your University.

Key Responsibilities will include, but are not limited to the following:

Evaluate the innovative statistical methodology and implementation on oncology clinical trials

Perform the clinical study data review, checking and analysis using SAS, R, and/or other statistical software.

Showcase your work with a final poster board presentation near the conclusion of your internship

Must be at least 18 years old

Must have a minimum GPA of 2.8

Knowledge of IT security, quality and risk management requirements relevant to assigned domain

Knowledge of best practices in IT or related project management, continuous improvements and change management

Oversees and manages or otherwise leads business / user requirements gathering / needs analysis

Oversees and manages or otherwise leads analysis for initial business case, resource requirements, categorization, and prioritization

Thorough knowledge of Agile and proven abilities to apply these to support IT solutions to meet business needs and objectives

Thorough knowledge of key programming languages and requirements relevant to assigned domain

Ability to use problem solving skills to deduce business requirements and translate into technical solution

Excellent communication skills and the ability to transfer requirements clearly

Key Responsibilities will include, but are not limited to the following:

Build end-to-end data science and engineering solutions utilizing Artificial Intelligence and Machine Learning within a small, dynamic team.

Work cross-functionally with stakeholders in PDM and/or Gilead more broadly.

Support the team by developing innovative methods using advanced engineering and mathematical techniques

Good conflict management and negotiation skills.

Assist with Federal and State Sunshine reporting and related healthcare compliance posting requirements as needed.

5 years of compliance experience in a biotech/pharma organization.

Experienced in assisting the development, initiation, and maintenance of policies and procedures for the operation of a Compliance Program.

Demonstrated experience working cross functionally within organization.

Monitoring and auditing experience preferred.

Strong project management skills, including attention to detail and organization skills

Project and process management of Gilead eCTs, CTs, Global Strategic Marketing teams, primarily in the oncology and inflammation therapeutic areas

Serve as key process and thought partner to eCT and CT leaders, head of GCO Project Management lead

Partner with head of GCO Project Management to identify areas for process efficiency across eCTs, CTs, and overall teams system

Partner with head of GCO Project Management on Annual Planning team.

Associate Director- Project Management, Planning and Operations

Demonstrated excellence in program management, project management, change management and effectively managing multiple projects/priorities.

Bachelor’s Degree with Twelve years’ experience

Master’s Degree with Ten years’ experience

PhD and Eight years’ experience

Ability to demonstrate strong negotiation and influencing skills and relationship building for credibility.

Global experience in-country role working with a global strategy or directly in a global role.

Personnel development, coaching and performance management

Review architectures, safety requirements and safety analyses of your team

Collaborative team player with strong written and in-person communication skills

Hands-on experience of defining, applying and coordinating safety analysis techniques such as HARA, FMEA, FTA in safety-related fields

Experience developing safety-related hardware or software across full development cycle

Experience in working with complex architectures and boosting safety integrity of non-safety components

Help deliver the required PDM inputs to the Gilead Enterprise Risk Management review and execute on that process.

Experience in the biotech or pharmaceutical industry with demonstrated cross-functional collaboration and leadership; deep knowledge about the biotech / bio-pharma segment.

Develop and manage PDM CAPEX plans, including evaluating critical spending tradeoffs and major project approvals. .

Bachelor’s degree and 12+ years of relevant experience, or master’s degree / PhD / MD with 10+ years of relevant experience.

Experience working across different cultures.

Strong leadership, self-direction, comfort and experience tackling ambiguous, complex problems.

Multiple years’ CDM or other data analytics / data management experience, including experience leading small projects and project teams.

Acts as a point of contact for study management teams and for Clinical Development regarding data management issues.

Ensures adherence to standard business processes within CDM systems to assure compliance with regulatory requirements.

Trains and mentors less experienced in colleagues in CDM processes, projects, programs and tools.

Adheres to regulatory requirements, industry standards and Gilead SOPs and ensures the same across own team.

Demonstrates strong facilitation / presentation skills and ability to appropriately delegate tasks to others.

Understanding the impact of decisions and actions on the business and consulting with colleagues and management as applicable

Thorough knowledge of current and emerging scientific standards regulatory requirements for assigned territories

Evaluating departmental and broader organizational SOPs as fit for purpose, in compliance with current scientific standards and regulatory requirements

Excellent written and oral communication skills and ability to convey complex technical information clearly

Previous Virology therapeutic area experience

Eligible employees may participate in benefit plans, subject to the terms and conditions of the applicable plans.

Strong presentation and interdepartmental change management communication skills is required to excel in this role.

This role requires knowledge and experience in office and lab occupancy planning.

Required Years of Experience: 3-5 years

Top 3 Required Skill Sets

Top 3 Nice to Have Skill Sets

Required Degree or Certification: Bachelor's Degree in Architecture, Engineering, or other relevant fields

• Provide administrative support in terms of coordination for project contracting and management.

• Strong background and experience in epidemiological, observational and/or implementation research methods

• Strong verbal and written communication skills

• Experience working in SAS, STATA and/or qualitative data analysis softwared packages preferred.

• Relevant research experience with a strong focus on epidemiological, observational and/or implementation research

We have the following exciting opportunity in our Foster City, CA location:

Provide administrative support in terms of coordination for project contracting and management.

Strong background and experience in epidemiological, observational and/or implementation research methods

Strong verbal and written communication skills

Experience working in SAS, STATA and/or qualitative data analysis softwared packages preferred.

Relevant research experience with a strong focus on epidemiological, observational and/or implementation research

Excellent written/oral communication skills, in particular scientific writing