Atlas Hiring for Epidemiology Associate Job at Remote Full Time

Job Title: Epidemiology Associate II
Job Location: Boston, MA
Job Duration: 12 Months for Fortune 500 client

Job Description

• The Epidemiology Associate is a strategic and scientific role accountable for developing, coordinating, and executing cutting-edge, effective, and impactful epidemiology deliverables for their assigned registry.
• The Epidemiology Associate will lead their assigned registry in project planning, management, and execution of epidemiology deliverables to ensure efficient and accurate completion within budget and timelines, and in accordance with current epidemiology and pharmacoepidemiology methodology.
• The Epidemiology Associate is accountable the execution of deliverables individually or through oversight of vendors.
• The Epidemiology Associate will routinely interact with therapeutic area lead Epidemiologists within the department.
• The Epidemiology Associate will participate in cross-functional Registry Leadership Teams and will lead sub-team meetings with Registry Biostatisticians and Programmers.
• The Epidemiology Associate will work closely with registry stakeholders across Medical Affairs, Pharmacovigilance, Regulatory Affairs, and Clinical Development and must have mature team-working behaviors and organizational awareness and insight.
• The Epidemiology Associate may also interact with external stakeholders to ensure appropriate communication of epidemiological issues and study results, including Scientific Advisory Board members and regulatory authorities.
• Strong project planning, management, and execution ability, along with excellent communication skills, both written and oral are essential.

Responsibilities

• Accountable to propose, design, initiate, and report epidemiologic study analyses for their assigned Registry.
• Accountable to lead the project planning, management, and execution of epidemiology deliverables for their assigned Registry.
• Accountable for providing epidemiology support to Medical Affairs, Pharmacovigilance, Regulatory Affairs, and Clinical Development related to their assigned Registry.
• Active participation on cross-functional Registry Leadership Teams.
• Lead sub-team meetings with Registry Biostatisticians and Programmers as appropriate.
• Accountable for providing epidemiology perspective into study protocols, case report forms (CRFs), and regulatory documents and other reports for their assigned Registry.
• Interact with authors, referees, and in-house reviewers on scientific manuscripts, clinical conference abstracts, presentations, and posters based on data generated from their assigned Registry.
• May represent Epidemiology department during interactions with key external stakeholders including Registry Scientific Advisory Boards and regulatory authorities.

Required Experience

• Excellent oral and written communication skills
• Knowledge of drug and clinical development process
• Excellent attention to detail and quality, and scientific rigor
• Ability to work under pressure and lead by example
• Strong interpersonal skills and ability to work effectively in multidisciplinary teams
• Thorough and up-to-date technical knowledge of epidemiology and biostatistics methods
• Experience and familiarity using SAS for statistical analysis
• Record of high-quality publications in peer-reviewed journals

Required Skills

• Biostatistics/Epidemiology
• Statistical Analysis
• Biotechnology
• SAS
• Project Planning

Desired Skills

• Excellent Communication Skills
• Budget
• Case Report
• Case Report Forms
• Pharmacovigilance
• Regulatory Affairs
• Serial Attached Scsi
• Regulatory Documents
• Therapeutic

Education

• At least 3 years of industry experience in the pharmaceutical industry, biotechnology, or consulting environment for Doctoral-level candidates, or 6 years of industry experience for Master’s-level candidates.
• PhD / DSc / DrPH in Epidemiology with 3 years of industry experience, or MPH / MSc in Epidemiology with 6 years of industry experience

Job Types: Full-time, Contract

Pay: $80.00 – $89.00 per hour

Benefits:

• 401(k)

Schedule:

• 5×8
• 8 hour shift
• Day shift
• Monday to Friday
• No nights

Education:

• Master’s (Preferred)

Experience:

• drug and clinical development process: 5 years (Required)
• epidemiology and biostatistics methods: 4 years (Required)
• SAS /Statistical Analysis: 3 years (Preferred)
• pharmaceutical industry: 6 years (Required)

Work Location: Remote