AstraZeneca Posted August 19, 2026

Senior Scientist, Clinical Imaging Scientist

Cambridge, Massachusetts, United States of America Full time
Drug Discovery & Preclinical Research Senior

AstraZeneca is the source of truth for this posting and owns the application process. We surface normalized context and market comparison you won't find on the original listing.

About this opportunity

Fusion Pharmaceuticals, a member of the AstraZeneca Group, is a clinical-stage oncology company focused on developing next-generation radioconjugates (RCs) as precision medicines. Fusion connects alpha particle emitting isotopes to various targeting molecules to selectively deliver the alpha emitting payloads to tumors. Fusion’s clinical portfolio includes but is not limited to: FPI-2265 targeting prostate specific membrane antigen (PSMA) for metastatic castration resistant prostate cancer currently in a Phase 2 trial; FPI-1434 targeting insulin-like growth factor 1 receptor currently in a Phase 1 trial; and FPI-2068, a bispecific IgG-based EGFR cMET targeted radioconjugate currently in a Phase 1 trial.

Fusion has multiple other pipeline programs that will soon be entering into early FIH trials. In addition, Fusion is pursuing combination programs between RCs and other therapeutic modalities including DNA Damage Response Inhibitors (DDRis) and immune-oncology agents. To support execution for these programs, Fusion has a fully operational Good Manufacturing Practice (GMP) compliant state-of-the-art radioconjugate manufacturing facility to meet supply demand for our growing pipeline of RCs.

Candidates for the Nuclear Medicine Technologist, Thernostics and Radiation Science role need to work on a hybrid basis out of our Cambridge, Massachusetts office.

Responsibilities

Assist in the development of, and adherence to, imaging trial documents (e.g., Image Review Charter, Imaging Manual, Data Transmittal Forms, and Dosimetry Manuals).

Provide subject matter expertise to internal and external stakeholders in matters of image acquisition, storage, review, and processing.

Maintain an archive of imaging related data for ongoing and completed trials.

Collaborate with clinical operations in the oversight, conduct and management of imaging-related aspects of clinical studies in accordance with the clinical protocol, study manuals and plans, and timelines while ensuring quality in accordance with GCP and ICH guidelines.

Assist with the management of in-house processing of image data and internal dosimetry efforts to support ongoing research and multi-disciplinary department and company initiatives.

Provide support for clinical data review; assist in generation of clinical research reports and presentations including abstracts, posters, and publications.

Provide support to clinical site staff and investigators pertaining to preparation, administration, and waste management of imaging and therapeutic radiopharmaceuticals.

Respond to radiation safety questions and concerns regarding the use of diagnostic and therapeutic radiopharmaceuticals and precautions.

Have a working knowledge and understanding of modern electronic infrastructures relevant to radiological imaging such as DICOM, PACS, IHE models, image processing and advanced visualization.

Willingness to travel when needed (5-10%)

Qualifications

The candidate should have a Bachelor of Science degree with a life science focus from an accredited educational institution and NMTCB/ARRT(N) certification in nuclear medicine or equivalent. Additional training in radiation safety (NMTCB(RS)) and/or medical physics with an advanced master's qualifications is preferred but not required.

Minimum of at least 5 years of clinical experience.

Experience working in clinical trials for 2-5 years is preferred but not required.

Demonstrated technical and analytical problem-solving skills.

Scientific expertise in SPECT and PET imaging is recommended, including acquisition, reconstruction and uploading of images.

Training in Good Clinical Practices (GCP), Quality Assurance/Compliance (QA/QC) in a clinical trial setting is preferred.

Experience with radioactive materials license amendment process with the NRC and Agreement States.

Familiar with Radiation Safety Officer (RSO) responsibilities.

Ability to clearly articulate and present the role and impact of molecular imaging on decision making within drug discovery and development.

Self-motivation and exceptional verbal and written communication skills.

Ability to multi-task and work effectively in a team or independently on assigned tasks.

Proficiency in business computer skills and experience with medical imaging workstations

(i.e., MIM), dosimetry software, and/or PACS preferred.

All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran.

The annual base pay for this position ranges from $118,870.40 to $178,305.60. Our positions offer eligibility for various incentives, an opportunity to receive short-term incentive bonuses, equity-based awards for salaried roles and commissions for sales roles. Benefits offered include qualified retirement programs, paid time off (i.e., vacation, holiday, and leaves), as well as health, dental, and vision coverage in accordance with the terms of the applicable plans.

Date Posted

19-Aug-2026

Closing Date

11-Sep-2026 Our mission is to build an inclusive environment where equal employment opportunities are available to all applicants and employees. In furtherance of that mission, we welcome and consider applications from all qualified candidates, regardless of their protected characteristics. If you have a disability or special need that requires accommodation, please complete the corresponding section in the application form.

Job details

Seniority
Senior
Function
Drug Discovery & Preclinical Research
Therapeutic area
Not listed
Location
Cambridge, Massachusetts, United States of America
Employment type
Full time

How this role compares

Computed from every other active Drug Discovery & Preclinical Research role in our database, not just this employer's listings.

We currently track 190 comparable Senior Drug Discovery & Preclinical Research roles across 31 biopharma companies.

190Comparable roles tracked
179Currently active
31Companies hiring similar roles
10Countries represented

Salary context

64 of 190 peers report a salary range (USD, annualized)

Peers share this role's job function and a matching or adjacent seniority level -- not necessarily the same therapeutic area or country.

This roleSubject Not listed on this posting
Lowest disclosed · Senior Research Associate, Analytical Operations · Gilead Sciences, Inc. $94,945/yr – $122,870/yr
Peer group range $108,908 – $269,350 (median $172,150)

Where these roles are based

Top locations among the 190 comparable roles

United States156
India8
Germany7
Canada4
United Kingdom4
China4

+ 4 more countries

Seniority mix

190 of 190 peers have a known seniority level

Senior102
Principal64
Associate Director24

Therapeutic area mix

32 of 190 peers have a known therapeutic area; the rest are genuinely unlabeled, not hidden

Oncology17
Cardiovascular / CVRM9
Immunology3
Neuroscience2
Respiratory1

Similar opportunities

The closest matches from our peer group, ranked by how similar they are, not how well you'd qualify for them -- treat this as market context, not a guaranteed shortlist; a weak match is labeled as one below.

60%similar
Lilly Indianapolis, Indiana, United States of America Senior
Same function Same seniority Same country
60%similar
Lilly Indianapolis, Indiana, United States of America Senior
Same function Same seniority Same country
60%similar
Merck West Point, Pennsylvania, United States of America Senior
Same function Same seniority Same country
60%similar
Merck South San Francisco, California, United States of America Senior
Same function Same seniority Same country
60%similar
Merck Cambridge, Massachusetts, United States of America Senior
Same function Same seniority Same country
60%similar
Pfizer Groton, United States Senior
Same function Same seniority Same country

Notify me about similar jobs

Get an email when we spot other openings like this one – same job function, comparable seniority, roles you'd actually want to see.

How we calculate "similar"

No black box, no LLM guesswork: a deterministic score built from four normalized attributes. Here's this role's own peer group at different match levels, so you can see the mechanism, not just the result.

Every comparison starts from the same 100-point budget: 25 for working in the same function, 40 for the same therapeutic area, 20 for the same or adjacent seniority, 15 for the same country. A dimension we can't confirm on both sides contributes nothing, never a guess, never a free pass.

60%
Scientist/Sr Scientist, Discovery Strategy and Operations
Lilly · Indianapolis, Indiana, United States of America · Senior
Function Therapeutic area Seniority Country
60%
Senior Scientist, Antibody Discovery
Merck · South San Francisco, California, United States of America · Senior
Function Therapeutic area Seniority Country
60%
Senior Scientist - Structural Biology and Protein Sciences
Pharmacia & Upjohn Company · San Diego, United States · Senior
Function Therapeutic area Seniority Country
60%
Senior Scientist l, QTAS & ADME Sciences
AbbVie · North Chicago, IL · Senior
Function Therapeutic area Seniority Country
Unmatched or unknown dimensions score exactly the same: 0 points, never a partial guess. A role we know almost nothing about beyond its function bottoms out at 25%; it never inflates to 100% just because there's little to compare against. Seniority uses a defined ladder (Associate → Manager → Associate Director → Senior → Principal → Director → Senior Director → Executive/VP) so "Director" and "Senior Director" count as adjacent, but "Director" and "Executive/VP" do not.