Celea Therapeutics Posted October 9, 2026

Clinical Scientist, Director

Boston Type not listed
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Celea Therapeutics 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

As we prepare for our next stage of growth and clinical advancement, Celea is a highly motivated and collaborative Clinical Scientist to join the clinical development team. Reporting to the VP, Head of Clinical Development, this role will work closely with Clinical Development, Clinical Operations, Medical Affairs, and external partners to support the planning, execution, and interpretation of clinical studies. A key component of the role will be working closely with our CRO partners, helping to ensure high-quality study execution, timely delivery of clinical data, and alignment with the clinical development strategy.

This position is based in Boston, remote/hybrid friendly.

The ideal candidate is scientifically rigorous, highly organized, comfortable working in a fast-paced environment, and able to operate effectively with both internal stakeholders and external vendors.

Key Responsibilities

Support the development and execution of clinical development strategies and plans.

Contribute to clinical study design and implementation, including development of study concepts, protocols, schedules of assessments, medical monitoring plans and related clinical documents including investigator and site training materials.

Conduct ongoing review and interpretation of clinical safety data and identify emerging trends, issues, and opportunities both in real-time and for aggregate review.

Support clinical data review, including review of listings, tables, and figures.

Partner with Clinical Operations and Data Management to identify and resolve data quality issues.

Contribute to clinical study reports, regulatory documents, presentations, and other clinical development deliverables.

Work closely with CRO clinical teams to support study planning, execution, and delivery.

Review and provide input on CRO deliverables, including study plans, protocols, data review materials, and clinical reports.

Help identify and escalate study issues and work collaboratively with CRO partners to develop solutions.

Qualifications

Required

PhD, PharmD, MS or advanced scientific degree in a relevant discipline.

8+ years of relevant experience in clinical development , clinical research, or a related pharmaceutical/biotechnology environment.

Experience supporting clinical trials in a biotechnology or pharmaceutical company including reviewing, aggregating and synthesizing blinded safety data and troubleshooting missing data and assessments, and reviewing risk-based monitoring output

Experience working directly with CROs and other external clinical development partners.

Understanding of clinical trial methodology, clinical development processes, and GCP principles.

Strong scientific writing and communication skills.

Excellent organizational and project-management skills.

Entrepreneurial mindset and comfort operating in a fast-paced, early-stage environment.

Proficiency using AI tools to work smarter, curiosity about how technology can improve the quality and speed of your work.

Preferred

Respiratory disease area experience is preferred.

Experience with Phase 1–3 clinical development.

Experience supporting regulatory submissions or interactions.

Experience working with external investigators.

Why Join Celea Therapeutics

Play a pivotal role in advancing life-changing therapies for patients with devastating lung diseases.

Shape the foundation of a Phase 3 biotech poised for significant growth.

Collaborate with a passionate, mission-driven leadership team.

Competitive compensation and equity package.

Compensation

Transparency is one of our values, and that includes how we pay. The anticipated salary range for this role is $225,000 - $240,000 plus bonus and equity. Where an offer lands within the range reflects the candidate’s experience, skills, and internal equity, and we welcome open conversations about compensation from the first call, so there are no surprises at the offer stage.

Actual compensation will be determined based on experience, qualifications, and location.  In addition to base pay, this role is eligible for bonus and equity compensation.

Base Pay Information

$225,000, $240,000 USD

Job details

Seniority
Director
Function
Clinical Development
Therapeutic area
Not listed
Location
Boston
Employment type
Not listed

How this role compares

Computed from every other active Clinical Development role in our database, not just this employer's listings.

We currently track 311 comparable Director Clinical Development roles across 53 biopharma companies.

311Comparable roles tracked
296Currently active
53Companies hiring similar roles
17Countries represented

Salary context

163 of 311 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 $225,000/yr – $240,000/yr
Lowest disclosed · Patient Safety, Medical Director · Vertex Pharmaceuticals Inc (US) $0/hr – $0/hr (≈ $0–$0/yr)
Peer group range $0 – $392,100 (median $264,000)

Where these roles are based

Top locations among the 311 comparable roles

United States251
United Kingdom17
India8
Switzerland7
Spain6
China3

+ 11 more countries

Seniority mix

311 of 311 peers have a known seniority level

Director218
Senior Director51
Principal42

Therapeutic area mix

93 of 311 peers have a known therapeutic area; the rest are genuinely unlabeled, not hidden

Oncology55
Immunology9
Neuroscience8
Cardiovascular / CVRM6
Respiratory6
Dermatology & Aesthetics3
Ophthalmology3
Vaccines & Infectious Disease2
Rare Disease1

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
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Open in 2 locations

Waltham, United StatesSouth San Francisco, United States

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%
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Function Therapeutic area Seniority Country
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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.