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Senior Associate, Investments (9770332

Job in New York, New York County, New York, 10261, USA
Listing for: Socket.dev
Full Time position
Listed on 2026-08-08
Job specializations:
  • Science
    Clinical Research, Data Scientist
Salary/Wage Range or Industry Benchmark: 180000 - 230000 USD Yearly USD 180000.00 230000.00 YEAR
Job Description & How to Apply Below
Position: Senior Associate, Investments (9770332)
Location: New York

TITLE:

Senior Associate, Investments (9770332)

EMPLOYER:

Roivant Sciences, Inc.

LOCATION:

New York, NY (A hybrid work schedule may be permitted within a commutable distance from the worksite, in accordance with company policies.)

DUTIES:
Gather, analyze, and summarize data on emerging drugs and therapies across biopharma. Build the scientific/clinical rationale and investment case for novel drug development ideas and acquisition targets by providing data to support deal negotiations, suggesting innovative clinical strategies, and identifying underappreciated biological targets overlooked by both investors and the biotech/pharma industry. Collaborate closely with Roivant’s R&D team—including non-clinical, clinical, Chemistry, Manufacturing, and Controls (CMC), and global regulatory (US FDA, EU EMA, Japan PMDA, China NMPA)—to interpret data from assets across the biotech value chain.

Analyze clinical trial data, assess methodologies and procedures, and present findings, predictions, and recommendations for further analyses. Build comprehensive clinical efficacy and safety databases to evaluate assets. Research the mechanisms of novel drugs by reviewing clinical trials, literature, and medical research, compiling relevant data for analysis. Use modeling techniques and analytical algorithms to predict drug success, assess safety risks, and interpret advanced statistical methods to understand drug profiles.

Model pharmacokinetic/pharmacodynamic (PK/PD) profiles to optimize dosing strategies. Forecast therapeutic revenue through commercial launch modeling and revenue projections. Estimate development operating expenditures by understanding clinical trial design, statistical powering, endpoints, and related CMC constraints and costs. Review supply agreements and assess manufacturing risks across small molecules, large molecules, and inhaled products, including scale-up from early-stage to commercial supply. Perform analyses to evaluate asset return profiles to inform key decision makers.

Maintain relationships with biopharma companies and attend medical and business development conferences to stay current on research, clinical data, and to engage with potential partners. Source investment leads through private/public financing screens, emergent clinical data, and networking; maintain internal lead-tracking databases.

REQTS:
Must have a Bachelor’s degree or foreign equivalent in Human Evolutionary Biology, Biology, Chemistry, Bioengineering, or a related field plus three (3) years of buy-side experience in the biotech and pharma investing industry in the position offered or a related position. Must have three (3) years of experience with all of the following:
Analyzing clinical trial data using statistical models and methods, including Ancova, mixed model repeats, Student t-test, Chi-square, Mann-Whitney, Survival analysis, linear and logistic regression, Bayesian methods, and Meta analysis;
Applying statistical algorithms to interpret and predict outcomes based on clinical and pre-clinical data;
Reviewing, interpreting, and evaluating clinical trial methodologies, procedures, toxicology reporting, and data;
Using modeling techniques and predictive algorithms to assess drug efficacy and safety and to make data-driven recommendations about drug development and asset acquisition;
Data analysis, including compiling, analyzing, and summarizing complex datasets from clinical trials and scientific literature;
Conducting research on emerging drugs and therapies, including compiling relevant data from clinical trials, literature, and other medical research sources;
Assessing regulatory and ethical compliance of clinical trials and drug approval processes;
Performing analysis related to pharmaceutical assets, including risk assessment and value prediction to inform key decision makers;
Negotiating, structuring, and documenting deals for therapeutic assets, including milestones and equity issuance/dilution while balancing legal, financial, regulatory, geographic, and operational considerations.

HOURS:

40 hours per week, Monday-Friday, 9:00 AM-5:00 PM

SALARY: $180,000 to $230,000 per year

INCENTIVES OFFERED THROUGH THE EMPLOYEE REFERRAL AWARD PROGRAM ARE APPLICABLE TO THIS POSITION.

Roivant Sciences, Inc. provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state or local laws.

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Position Requirements
10+ Years work experience
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