Manager, Feasibility Analytics

Alnylam Pharmaceuticals; Cambridge (MA); On-site; USD 185,000 - 200,000; Full time

Job summary

A leading biopharmaceutical company in Cambridge, MA is seeking a Manager for Feasibility Analytics. This role focuses on developing data analysis methodologies for clinical trial feasibility insights, collaborates with key stakeholders, and ensures optimal operational strategies. Ideal candidates should possess strong analytical skills, experience in clinical data, and a background in biopharmaceuticals. A competitive salary and full-time position available.

Qualifications

• 2+ years experience in a CRO or biopharmaceutical company on multinational studies.
• Intermediate analytics and data storytelling skills.
• Proven ability to automate data processes.

Responsibilities

• Create and deliver feasibility data analytics packages.
• Monitor enrollment and startup for clinical trials.
• Provide improvements to feasibility data and analytics.

Skills

Data analysis

Data engineering

Project management

Analytical thinking

Communication skills

Problem-solving

Education

University Degree in Science, Computer Science, Informatics

Tools

Clinical trial management systems (CTMS)

Job description

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Overview

The Manager, Feasibility Analytics is responsible for developing thorough methods of data analysis for clinical trial feasibility insights, specific to indication, program, study, enrollment forecasting, country, and site feasibility across the Clinical Operations portfolio of clinical trials. He/she/they will partner within key stakeholders across the Feasibility Center of Excellence (CoE) to deliver feasibility analytics outputs used to derive optimized operational strategies. He/she/they will provide impactful insights while ensuring patients and participants are at the center of decision making.

The Manager, Feasibility Analytics is an intelligent and effective data-driven leader focused on the acquisition of data, data engineering, algorithm development, automation, and technology solutions to improve clinical trial decision making. The role is responsible for creating the analytics infrastructure for the future and broadening data culture and literacy across the Clinical Development organization to ensure effective delivery of Alnylam’s portfolio of studies.

He/she/they will work cross functionally with Clinical Portfolio Systems (CPS) and Information Technology (IT) to ensure timely and thorough global (end to end) feasibility outputs that are then utilized by the Feasibility Strategists to apply and influence key trial and program stakeholders. Technologies and data outputs owned by the Feasibility CoE are likely to be utilized across Expertise Areas (EAs) in addition to Clinical Operations (ClinOps). He/she/they consistently delivers high quality outputs and service to fulfill the most impactful suite of feasibility deliverables. He/she/they derives and develops epidemiology, market research, competitive intelligence, past performance, country and site intelligence, expertise, and innovative data and AI methodologies to ultimately drive improved decision making for successful trial enrollment outcomes.

The Manager, Feasibility Analytics is responsible for ensuring precise, predictive, and applicable data and insights packages working closely with the Feasibility Strategists. He/she/they provides data-driven assessments of protocol do-ability, patient voice, site and patient burden, study, country and site enrollment scenarios, country and site selection, and risk mitigation strategies to drive predictable and accelerated study execution of global clinical trials. This role works closely with other analytics colleagues and functions globally, both internal and external to Alnylam.

Key Responsibilities

• Creates and delivers consistent feasibility data analytics packages; inclusive of, but not limited to, historical / current clinical trials, epidemiology, standard of care, enrollment rates, start up timelines, enrollment forecasts, patient and site burden scores, site lists, site performance prediction, etc.
• Ensures on-time and high-quality of deliverables, specific to each stakeholder’s perspectives and needs.
• Routinely monitors enrollment and start up to indicate if clinical trials are performing to plan and then signaling when indicator thresholds are surpassed.
• Partners with stakeholders, CROs, and vendors to capitalize on historic study/site performance data, competitor trial performance, industry benchmarks, epidemiology, etc. using a variety of analytics and modeling tools to drive baseline study milestones targets/dates (CLOCK).
• Provides internal benchmarking and early forecasting to ensure proposed timelines and committed milestones are accurate and achievable.
• Drives improved KPI/metrics and intelligence to support process improvement and overall operational/business reporting.
• Provides improvements to feasibility data and analytics to improve the data infrastructure and usability of data to optimize clinical trials.
• In conjunction with Feasibility Strategists, derives impactful insights from data analyses.
• Optimizes operational delivery considering time, cost, quality, and burden and supports the data and outputs needed to baseline (CLOCK) the study assumptions.
• Effectively listens to stakeholders to understand problem statements and ascertain data to answer key questions for trial optimization.
• Continually improves the overall feasibility strategy and process to be flexible, yet systematic across the pipeline.
• Drives a patient-and-site-first mindset throughout the organization to create more successful, inclusive, and optimized clinical trials.

Qualifications

• University Degree in Science, Computer Science, Informatics, or related discipline. A higher degree is desirable.
• Intermediate (2+ years) previous experience gained with a CRO or biopharmaceutical company working on multinational clinical studies
• Intermediate analytics and data storytelling skills
• Proven ability to automate data processes and analytics
• Proven skills in innovation and scaling technologies
• Proven ability to lead within a matrixed team
• Experience in clinical research, data analytics, and data evaluation
• Experience with global data sets
• Intermediate verbal and written communication skills
• Strong problem-solving skills
• Well developed interpersonal skills, including ability to persuade, negotiate, and moderate conflict
• Strong project management skills with the ability to manage multiple projects simultaneously.
• Familiarity with clinical trial management systems (CTMS) and data flows of external data sources.
• Ability to travel up to 10%.

Requirements

• Must be self-motivated and able to work independently and successfully.
• Able to prioritize effectively with good problem‑solving and planning abilities
• Strong organizational skills and ability to deal with competing priorities.
• Excellent communication and interpersonal skills, with the ability to effectively collaborate with internal and external stakeholders at all levels, including ability to persuade, negotiate, and moderate conflict.
• Ability to analyze complex data and provide actionable insights to drive decision-making.
• Proven ability to build and maintain strong relationships with key stakeholders, including Clinical Research, Regulatory, Epidemiology, Portfolio and Program Management, Commercial, Medical Affairs, Study Start Up, CROs, Study Management, and other Clinical Operations functions.
• Critical reasoning skills including the identification and resolution of complex problems
• Willingness and proven ability to work flexibly stepping outside of immediate role responsibilities and wear ‘multiple-hats’ where needed.
• Confident and has the professional competence to win respect and gain credibility at all levels within and outside the company; capable of representing the company externally.
• Strategic Thinking: General knowledge of all major aspects of drug discovery and development along with effective departmental leadership to be an effective problem solver for complex problems.

About Alnylam: We are the leader in RNAi therapeutics – a revolutionary approach with the potential to transform the lives of people with rare and common diseases. Built on Nobel Prize-winning science, Alnylam has delivered the breakthroughs that made RNAi therapeutics possible and are just at the beginning of what’s possible. Our deep pipeline, late-stage programs, and bold vision reflect our core values: fierce innovation, passion for excellence, purposeful urgency, open culture and commitment to people. We're proud to be a globally recognized top employer, where an authentic, inclusive culture and breakthrough thinking fuel one another.

At Alnylam, we commit to an inclusive recruitment process and equal employment opportunity. Qualified applicants will receive consideration for employment without regard to their sex, gender or gender identity, sexual orientation, race, color, ethnicity, national origin, ancestry, citizenship, religion, creed, physical or mental disability, pregnancy status or related conditions, genetic information, veteran or military status, marital or familial status, political affiliation, age, or any other factor protected by federal, state, or local law. Alnylam is an E-Verify Employer.

Seniority level

• Seniority level

  Mid-Senior level

Employment type

• Employment type

  Full-time

Job function

• Job function

  Research, Analyst, and Information Technology

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