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Orum Therapeutics

Project Team Leader, Biology

lexington, MA

Check who can apply and the requirements below before continuing.

About this opportunity

Orum Therapeutics lists this Project Team Leader, Biology opportunity in lexington, Massachusetts. Review the employer’s description below for duties, qualifications and application requirements.

Job description

Lead the biology strategy and execution for one or more oncology discovery programs spanning target validation, hit-to-lead, lead optimization, and IND-enabling studies

Design and oversee in vitro and in vivo plans for degrader and degrader antibody conjugate candidates

Serve as the biology representative on cross-functional project teams with chemistry, DMPK, toxicology, CMC, and translational functions

Translate research strategy into workplans, timelines, and go/no-go criteria; anticipate risks and propose data-driven mitigations

Coordinate and oversee in vivo studies, including scoping, CRO selection and management, dosing design, and data integrity

Mentor and provide scientific guidance to junior scientists

Analyze, interpret, and communicate data and program status to research leadership and the broader organization

Contribute to target evaluation, portfolio strategy, and new program concepts

Requirements

PhD in cancer biology, molecular/cell biology, pharmacology, biochemistry, or a related field, with 8+ years of experience, or a Master's degree with 12+ years of commensurate experience

Demonstrated record of independently leading discovery programs

Demonstrated track record advancing oncology discovery programs toward IND

Program-level or hands-on experience with targeted protein degradation, including E3 ligase biology, molecular glues and/or PROTACs, ternary complex formation, and degradation assays

Experience with antibody-drug conjugates, including target/antigen selection, internalization, linker-payload biology, DAR, bystander effect, and characterization

Ability to design and interpret in vivo oncology pharmacology studies, including xenograft/PDX, PK/PD, and efficacy

Experience managing CRO-run studies

Strong record of cross-functional collaboration across discovery and development

U.S. citizenship or authorization to work in the U.S.; employer unable to sponsor or transfer at this time

Ability to pass a background investigation

Core Competencies

Expertise in leading oncology discovery programs, including target validation and IND-enabling studies, with a strong focus on targeted protein degradation and antibody-drug conjugates. Proven ability to mentor junior scientists and collaborate cross-functionally to drive research strategy and execution.

Highest-signal resume keywords

PhD In Cancer Biology

Targeted Protein Degradation

Antibody-Drug Conjugates

In Vivo Oncology Pharmacology Studies

Cross-Functional Collaboration

ATS Optimization Keywords

Hard Skills

Target Validation

Hit-To-Lead

Lead Optimization

IND-Enabling Studies

E3 Ligase Biology

Molecular Glues

Degradation Assays

Xenograft/PDX Studies

PK/PD Analysis

Efficacy Studies

Soft Skills

Mentoring

Scientific Guidance

Data Communication

Industry Keywords

Oncology

Pharmacology

Biochemistry

Molecular Biology

Cancer Biology

Tools & Technologies

CRO Management

Dosing Design

Data Integrity

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Worksite address

lexington, MA, 02173, US

Who can apply

Review the original listing for work authorization, qualifications and employer requirements.

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