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Abdera Therapeutics

via Jazzhr

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Contractor - CMC Project Manager

Anywhere
Contract
Posted 1/30/2026
Direct Apply
Key Skills:
Project Management
Cross-functional Collaboration
Regulatory Knowledge

Compensation

Salary Range

$NaNK - NaNK a year

Responsibilities

Lead and coordinate CMC activities across development stages, manage project plans, timelines, budgets, and external vendors, and support regulatory submissions.

Requirements

Bachelor's in science or engineering, 5+ years in CMC or biotech project management, experience with external vendors and regulatory requirements, proficiency with project management tools, PMP preferred.

Full Description

Who we are Abdera Therapeutics Inc. is a precision oncology company developing next-generation targeted radiation therapies- one of the most cutting-edge and highly promising areas of drug development. The company is built on a proprietary modular technology platform optimized for the delivery of radioisotopes to selectively destroy tumor cells while sparing healthy cells. Abdera is using this platform to enable the rapid development of a broad range of safe and efficacious therapies serving cancer patients with limited treatment options. Abdera Therapeutics is growing rapidly and seeking key new team members who thrive at the cutting-edge of innovation. Come join us and be a part of the ground-breaking team set to unlock the power of targeted radiotherapy! What we look for At Abdera Therapeutics, we are looking for curious and committed individuals who are ready for the opportunity to transform the way people living with cancer can be treated. We are relentless in our focus to offer new hope to families facing devastating diagnoses. We are in search of team members who work collaboratively with a diverse group of colleagues, respectfully engaging one another while collectively and inclusively tackling any challenges we may face. We are building an exciting and fast paced company passionate about discovering and developing tomorrow’s most innovative cancer therapies. Abdera is seeking a CMC Project Manager, Contractor who will support and coordinate CMC activities across development programs. Principal Responsibilities Lead cross-functional CMC project planning and execution from early development through commercialization Develop and maintain integrated CMC project plans, timelines, budgets, and risk registers Support program core teams in collaborating with program team lead Track milestones, dependencies, and critical path activities; proactively identify and mitigate risks Facilitate CMC team meetings, prepare agendas, document decisions, and drive follow-up actions Serve as primary CMC point of contact for program teams and senior leadership Plan and manage CMC contributions to regulatory submissions in collaboration with regulatory and program leads as needed Oversee work with CDMOs and external partners, including scope, timelines, and deliverables Prepare clear project updates, dashboards, and summaries Support continuous improvement of CMC project management processes and tools Other related duties as assigned. Qualifications, Education & Experience Bachelor’s degree in science, engineering, or related field (advanced degree preferred) 5+ years of experience in CMC, technical operations, or pharmaceutical/biotech project management Strong understanding of phase appropriate CMC development, manufacturing, and regulatory requirements Proven ability to manage complex, cross-functional projects in a regulated environment Experience working with CDMOs and external vendors Excellent organizational, communication, and stakeholder-management skills Proficiency with project management tools (e.g., MS Project, Smartsheet, or similar) Experience supporting early to late-stage development programs Familiarity with global regulatory expectations (FDA, EMA, ICH) Experience working in start-up environment preferred PMP or other project management certification Experience in biologics, oncology, or manufacturing (as applicable) Skills and Abilities Ability and drive to creatively solve practical problems Excellent written and verbal communication and strong organizational and time management skills Strong execution and follow-through Ability to balance detail with big-picture program objectives Comfortable operating in fast-paced environment Strong sense of planning and prioritization, and the ability to work with all levels of management Detail oriented, exceptional documentation practices, technical writing and oral communication skills, ability to identify, communicate and recommend solutions to complex problems Collaborative, proactive, and solutions-oriented mindset Abdera is an equal opportunity employer that is committed to diversity and inclusion in the workplace. At Abdera, we prohibit harassment of any kind and any form of discrimination including but not limited to discrimination based on race, color, sex, religion, marital status, sexual orientation, national origin, disability, veteran status, genetic information, pregnancy, or any other protected characteristic as outlined by federal, state, or local laws. This commitment is applicable to all employment practices within our organization, including hiring, recruiting, promotion, termination, layoff, recall, leave of absence, compensation, benefits, training, and apprenticeship. Who we are Abdera Therapeutics Inc. is a precision oncology company developing next-generation targeted radiation therapies- one of the most cutting-edge and highly promising areas of drug development. The company is built on a proprietary modular technology platform optimized for the delivery of radioisotopes to selectively destroy tumor cells while sparing healthy cells. Abdera is using this platform to enable the rapid development of a broad range of safe and efficacious therapies serving cancer patients with limited treatment options. Abdera Therapeutics is growing rapidly and seeking key new team members who thrive at the cutting-edge of innovation. Come join us and be a part of the ground-breaking team set to unlock the power of targeted radiotherapy! What we look for At Abdera Therapeutics, we are looking for curious and committed individuals who are ready for the opportunity to transform the way people living with cancer can be treated. We are relentless in our focus to offer new hope to families facing devastating diagnoses. We are in search of team members who work collaboratively with a diverse group of colleagues, respectfully engaging one another while collectively and inclusively tackling any challenges we may face. We are building an exciting and fast paced company passionate about discovering and developing tomorrow’s most innovative cancer therapies. Abdera is seeking a CMC Project Manager, Contractor who will support and coordinate CMC activities across development programs. Principal Responsibilities Lead cross-functional CMC project planning and execution from early development through commercialization Develop and maintain integrated CMC project plans, timelines, budgets, and risk registers Support program core teams in collaborating with program team lead Track milestones, dependencies, and critical path activities; proactively identify and mitigate risks Facilitate CMC team meetings, prepare agendas, document decisions, and drive follow-up actions Serve as primary CMC point of contact for program teams and senior leadership Plan and manage CMC contributions to regulatory submissions in collaboration with regulatory and program leads as needed Oversee work with CDMOs and external partners, including scope, timelines, and deliverables Prepare clear project updates, dashboards, and summaries Support continuous improvement of CMC project management processes and tools Other related duties as assigned. Qualifications, Education & Experience Bachelor’s degree in science, engineering, or related field (advanced degree preferred) 5+ years of experience in CMC, technical operations, or pharmaceutical/biotech project management Strong understanding of phase appropriate CMC development, manufacturing, and regulatory requirements Proven ability to manage complex, cross-functional projects in a regulated environment Experience working with CDMOs and external vendors Excellent organizational, communication, and stakeholder-management skills Proficiency with project management tools (e.g., MS Project, Smartsheet, or similar) Experience supporting early to late-stage development programs Familiarity with global regulatory expectations (FDA, EMA, ICH) Experience working in start-up environment preferred PMP or other project management certification Experience in biologics, oncology, or manufacturing (as applicable) Skills and Abilities Ability and drive to creatively solve practical problems Excellent written and verbal communication and strong organizational and time management skills Strong execution and follow-through Ability to balance detail with big-picture program objectives Comfortable operating in fast-paced environment Strong sense of planning and prioritization, and the ability to work with all levels of management Detail oriented, exceptional documentation practices, technical writing and oral communication skills, ability to identify, communicate and recommend solutions to complex problems Collaborative, proactive, and solutions-oriented mindset Abdera is an equal opportunity employer that is committed to diversity and inclusion in the workplace. At Abdera, we prohibit harassment of any kind and any form of discrimination including but not limited to discrimination based on race, color, sex, religion, marital status, sexual orientation, national origin, disability, veteran status, genetic information, pregnancy, or any other protected characteristic as outlined by federal, state, or local laws. This commitment is applicable to all employment practices within our organization, including hiring, recruiting, promotion, termination, layoff, recall, leave of absence, compensation, benefits, training, and apprenticeship.

This job posting was last updated on 2/2/2026

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