Top 611 Oncology data Jobs in Boston Ma

Clinical Trial Associate, Clinical Operations, Therapeutics and Oncology
Moderna, Inc. —Cambridge, MA
- $74,000 - $118,400 a year
- Full-time
- Mid-level
- Office
- Bachelor's degree
- Paid time off
- Adoption assistance
Clinical Research Associate II
AbbVie —Boston, MA
- $84,500 - $162,000 a year
- Full-time
- Remote
- Nursing
- Mid-level
- Organizational skills
- Paid holidays
- Health insurance
Protocol Associate – Oncology Clinical Research
ECOG-ACRIN Medical Research Foundation —Boston, MA
- $50,000 - $70,000 a year
- Full-time
- Hybrid work
- Mid-level
- Office
- Bachelor's degree
- Health insurance
- Dental insurance
Quick Apply
Associate Clinical Oncology Specialist
Natera —Boston, MA
- $110,000 - $130,000 a year
- Remote
- Nursing
- Mid-level
- Analysis skills
- Commuter assistance
- Health insurance
Program Administrator - Center for Neuroinclusive Oncology
Dana-Farber Cancer Institute —Boston, MA
- $77,290 - $92,690 a year
- Part-time
- Hybrid work
- 5 years
- Mid-level
- Office
Research Data Specialist II - Breast Oncology Translational Research
Dana-Farber Cancer Institute —Boston, MA
- $53,010 - $58,900 a year
- Full-time
- Computer literacy
- Mid-level
- Master's degree
Oncology Data Specialist – 32 hours/week, day shift
Beth Israel Lahey Health —Beverly, MA
- $27.00 - $36.34 an hour
- Full-time
- Anatomy knowledge
- Hospital
- Mid-level
Quick Apply
Research Data Specialist - Breast Oncology Translational Research
Dana-Farber Cancer Institute —Boston, MA
- $50,500 - $56,700 a year
- Full-time
- Computer literacy
- Mid-level
- Bachelor's degree
21h
Clinical Research Associate
Alliance for Clinical Trial in Oncology Foundation —Boston, MA
- $57,000 - $75,000 a year
- Full-time
- Hybrid work
- Microsoft Excel
- Bachelor of Science
- Mid-level
- Health insurance
- Dental insurance
Quick Apply
Research Associate, Immuno-Oncology Research
Moderna, Inc. —Cambridge, MA
- $63,200 - $100,900 a year
- Full-time
- Bachelor's degree
- US work authorization
- Communication skills
- Paid time off
- Adoption assistance
3d
Associate Computational Biologist
Dana-Farber Cancer Institute —Boston, MA
- $60,000 - $67,466 a year
- Full-time
- No experience needed
- Bachelor's degree
- In-person
Clinical Trial Manager
Generate Biomedicines —Somerville, MA
- $127,000 - $178,000 a year
- Remote
- Mid-level
- Bachelor's degree
- Travel
6d
Data Coordinator II, Research_BIDMC
Beth Israel Lahey Health —Boston, MA
- $21.64 - $34.62 an hour
- Full-time
- Customer service
- Computer literacy
- English
Senior Clinical Research Associate - US
Optimapharm d.o.o. —Boston, MA
- $100,000 - $130,000 a year
- Full-time
- Remote
- Nursing
- 5 years
- Computer literacy
- Dental insurance
- Paid time off
Administrative Specialist - Breast Oncology
Dana-Farber Cancer Institute —Boston, MA
- $50,070 - $60,730 a year
- Full-time
- Hybrid work
- Office
- High school diploma or GED
- Bachelor's degree
Computational Biologist — Multimodal and Foundation Models for Breast Cancer
Dana-Farber Cancer Institute —Boston, MA
- $75,000 - $91,500 a year
- Full-time
- Hybrid work
- Computer science
- Computer Science
- Mid-level
1d
Clinical Trial Associate
Candel Therapeutics —Needham, MA
- $88,000 - $100,000 a year
- Full-time
- Hybrid work
- Microsoft Excel
- Mid-level
- Bachelor's degree
Clinical Research Coordinator - Thoracic Oncology
Dana-Farber Cancer Institute —Brookline, MA
- $48,100 - $54,400 a year
- Full-time
- Mid-level
- Bachelor's degree
- Travel
Director, Oncology Data Science
Merck —Boston, MA
- $194,100 - $305,600 a year
- Full-time
- Analysis skills
- Math
- Doctor of Philosophy
- Paid holidays
- Health insurance
Administrative Support Specialist I: Breast Oncology
Dana-Farber Cancer Institute —Boston, MA
- $50,070 - $60,730 a year
- Full-time
- Hybrid work
- Office
- High school diploma or GED
- Bachelor's degree

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Clinical Trial Associate, Clinical Operations, Therapeutics and Oncology

Moderna, Inc. -
Cambridge, MA

Apply Now

Job Details

Full-time
$74,000 - $118,400 a year

Benefits

Paid time off
Adoption assistance

Qualifications

Regulatory compliance
ICH guidelines
Clinical quality assurance standards
Pharmaceutical research experience
FDA regulations

Full Job Description

The Role
The Clinical Trial Associate (CTA) provides clinical trial coordination support to Project Teams for assigned clinical trial(s).This support includes tracking a wide range of key operational activities and maintenance of essential study documentation, including the electronic Trial Master File (eTMF). with external vendors and CROs.The position reports to the Clinical Operations Head in the assigned Therapeutic Area and will work cross-functionally and collaboratively to support clinical operations activities.

Here’s What You’ll Do

Assist the Clinical Operations Lead(s) (COL) and/or Clinical Trial Manager(s) (CTM) in the day-to-day operational activities of assigned trials to ensure study objectives and timelines are met with quality, in compliance with applicable SOPs and regulatory guidelines
Maintain clinical trial files (including eTMF), project processes, tracking systems, and other utilized study or departmental systems
Liaise with Clinical Sample Management for the tracking and coordination of biomarker testing with 3rd party labs
Collaborate with Clinical Data Management and Digital Informatics to ensure timely training and access to Moderna systems (e.g., EDC, IWRS, ePRO, eTMF) for external stakeholders (e.g., CRO and Clinical Site Staff)
Coordinate Project Team and departmental meetings, including associated documentation
Assist with vendor / clinical site agreements, budgets and reconciliation / tracking of purchase orders and invoices for assigned trials
Develop and maintain strong, collaborative relationships with key stakeholders within Moderna, its CROs, and clinical sites

Here’s What You’ll Need (Basic Qualifications)

At least 2 years of experience in a clinical research environment
Bachelor’s degree in a science-based discipline preferred
Basic understanding of drug development, including familiarity with FDA and ICH GCP guidelines to ensure the appropriate conduct of clinical studies
Good verbal and written communication skills
Good organizational skills and attention to detail
Willingness to learn, able to take direction and ability to manage multiple tasks

Pay & Benefits

At Moderna, we believe that when you feel your best, you can do your best work. That’s why our benefits and well-being resources are designed to support you—at work, at home, and everywhere in between.

Competitive healthcare, plus voluntary benefit programs to support your unique needs
A holistic approach to well-being, with access to fitness, mindfulness, and mental health support
Family planning benefits, including fertility, adoption, and surrogacy support
Generous paid time off, including vacation, volunteer days, sabbatical, global recharge days, and a discretionary year-end shutdown
Savings and investment opportunities to help you plan for the future
Location-specific perks and extras

The salary range for this role is $74,000.00 - $118,400.00. This is the lowest to highest salary we in good faith believe we would pay for this role at the time of this posting. An individual’s position within the salary range will be based on several factors including, but not limited to, specific competencies, relevant education, qualifications, certifications, experience, skills, performance, and business or organizational needs.

The successful candidate may be eligible for an annual discretionary bonus, other incentive compensation, or equity award, subject to company plan eligibility criteria and individual performance.

About Moderna

Since our founding in 2010, we have aspired to build the leading mRNA technology platform, the infrastructure to reimagine how medicines are created and delivered, and a world-class team. We believe in giving our people a platform to change medicine and an opportunity to change the world.

By living our mission, values, and mindsets every day, our people are the driving force behind our scientific progress and our culture. Together, we are creating a culture of belonging and building an organization that cares deeply for our patients, our employees, the environment, and our communities.

We are proud to have been recognized as a Science Magazine Top Biopharma Employer, a Fast Company Best Workplace for Innovators, and a Great Place to Work in the U.S.

If you want to make a difference and join a team that is changing the future of medicine, we invite you to visit modernatx.com/careers to learn more about our current opportunities.

Our Working Model

As we build our company, we have always believed an in-person culture is critical to our success. Moderna champions the significant benefits of in-office collaboration by embracing a 70/30 work model. This 70% in-office structure helps to foster a culture rich in innovation, teamwork, and direct mentorship. Join us in shaping a world where every interaction is an opportunity to learn, contribute, and make a meaningful impact.

Moderna is a smoke-free, alcohol-free, and drug-free work environment.

Equal Opportunities

Moderna is committed to equal employment opportunity and non-discrimination for all employees and qualified applicants without regard to a person's race, color, sex, gender identity or expression, age, religion, national origin, ancestry or citizenship, ethnicity, disability, military or protected veteran status, genetic information, sexual orientation, marital or familial status, or any other personal characteristic protected under applicable law. Moderna is a place where everyone can grow. If you meet the Basic Qualifications for the role and you would be excited to contribute to our mission every day, please apply!

Moderna is an E-Verify Employer in the United States. We consider qualified applicants regardless of criminal histories, consistent with legal requirements.

Accommodations

We’re focused on attracting, retaining, developing, and advancing our employees. By cultivating a workplace that values diverse experiences, backgrounds, and ideas, we create an environment where every employee can contribute their best.

Moderna is committed to offering reasonable accommodations to qualified job applicants with disabilities. Any applicant requiring an accommodation in connection with the hiring process and/or to perform the essential functions of the position for which the applicant has applied should contact the Accommodations team at [email protected] .

Export Control Notice
This position may involve access to technology or data that is subject to U.S. export control laws, including the Export Administration Regulations (EAR). As such, employment is contingent upon the applicant’s ability to access export-controlled information in accordance with U.S. law. Due to the nature of the work and regulatory requirements, only individuals who qualify as U.S. persons (citizens, permanent residents, asylees, or refugees) are eligible for this position. For this role Moderna is unable to sponsor non-U.S. persons to apply for an export control license.
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Refine Your Search

oncology data jobs in boston ma

Clinical Trial Associate, Clinical Operations, Therapeutics and Oncology

Clinical Research Associate II

Protocol Associate – Oncology Clinical Research

Associate Clinical Oncology Specialist

Program Administrator - Center for Neuroinclusive Oncology

Research Data Specialist II - Breast Oncology Translational Research

Oncology Data Specialist – 32 hours/week, day shift

Research Data Specialist - Breast Oncology Translational Research

Clinical Research Associate

Research Associate, Immuno-Oncology Research

Associate Computational Biologist

Clinical Trial Manager

Data Coordinator II, Research_BIDMC

Senior Clinical Research Associate - US

Administrative Specialist - Breast Oncology

Computational Biologist — Multimodal and Foundation Models for Breast Cancer

Clinical Trial Associate

Clinical Research Coordinator - Thoracic Oncology

Director, Oncology Data Science

Administrative Support Specialist I: Breast Oncology

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