New · posted Oct 31
Celldex Therapeutics · Biotechnology
Global Clinical Project Leader
- New Haven, CT +1 more
- On-site
- Full-time
- Manager
The role
The Global Clinical Project Leader will provide overarching management of clinical trial execution for the assigned clinical development program. The incumbent will be responsible for developing the tactical portion of the operational component of the clinical development plan; in consultation with key stakeholders, including high level resourcing (timelines, budget, and resources), development of clinical project standards, tools, metrics, and assessing the impact of any proposed changes to the program. The incumbent will be responsible for employing risk-based management strategies, implementing solutions, and providing accurate and timely information on the program and fostering continuous improvement in clinical development.
What you need
- Completed BS degree or equivalent, with a minimum of 8 years pharmaceutical or biotechnology industry experience; or completed MS degree or equivalent with a minimum of 6 years pharmaceutical or biotechnology industry experience, at least 2 of which must have been at the Senior Clinical Trial Manager or equivalent position.
- Planning and managing complex and/or strategic priority clinical programs.
- Dermatology and Allergy experience preferred.
- Technology aptitude (project management, eTMF, etc.)
- Experience with data review, analysis, and interpretation of data.
- In-depth knowledge of the drug development and commercialization process (from protocol writing to medical results reporting and submissions.)
- In-depth knowledge of Good Clinical Practices (GCP), federal regulations and international regulations.
- Proven people management expertise.
- Ability to effectively influence without hierarchical authority.
- Flexibility and drive for results - willingness to embrace change and be able to work in a changing environment while being driven to achieve goals.
- Strong communication skills to ensure that project plans and status are transparent, and that risks, issues and results are clear to all parties involved.
- Strength and depth of skills in gathering information for decision-making; negotiation; and communicating decisions and actions.
- Able to work both independently and collaboratively across cultures and geographies.
- Strong computer skills including knowledge of Microsoft Excel, Word, and Outlook.
- Ability to work within established timelines, in a fast-paced environment.
- Excellent organizational and priority management skills.
- Good interpersonal skills and ability to deal with people at all levels with sensitivity and tact.
What you'll do
- Develop and deliver on operational component of the clinical development plan in consultation with key stakeholders, including:
- High level resource planning
- High level budget oversight
- Clinical drug supply requirements
- Development of clinical program standards; and
- Assessing impact of any proposed changes to the program
- Oversee matrix relationship with assigned Clinical trial Managers, Data Managers, and other members of the Clinical Project Team; ensure consistent execution across the program, deliver a development package of adequate quality for product registration.
- Represent development operations in cross-functional strategy and program team meetings.
- Detect possible operational issues/risks in the clinical development programs and assist CTMs in developing mitigation plans. Propose and implement solutions to issues/risks.
- Provide accurate and timely information on the program.
- Facilitate continuous improvement in clinical development.
- Stay abreast of clinical operations developments, methods, and technologies related to the biotechnology/pharmaceutical industry. Make strategic and tactical recommendations to provide and ensure competitive advantage to the company.
- Other job-related duties as assigned.
Pay and benefits
$176,659 – $229,427 a year
Employer providedThe expected base salary range for this position is $176,659 to $229,427We are committed to compensating employees equitably based on several factors including experience, education, licensure/certifications, skill level, location of the position, and availability of similar talent in a competitive market.
Annual discretionary bonus
Long term incentive
401(k) plan with employer contribution
Health care and other insurance benefits
Paid holidays
Vacation and sick days
Where you'll work
New Haven, CT +1 moreOn-siteOpen in Maps (opens in a new tab)
Also posted for: Hampton, NJ
More jobs in New Haven, CT +1 more
From the posting
About Celldex Therapeutics
About Celldex
Celldex is pioneering new horizons in immunology to deliver life-changing therapies. We are relentless in our pursuit of novel antibody-based treatments that engage the human immune system and directly affect critical pathways to improve the lives of patients with allergic, inflammatory and autoimmune disorders. We have built a culture where innovative and talented people thrive—focusing a significant effort on attracting and retaining passionate and motivated employees who want to play a role in helping people with serious health conditions and who see this effort as personally rewarding. In our highly entrepreneurial environment, employees are empowered and the opportunity for professional development occurs every day.
Equal opportunity, accessibility and legal noticesCelldex Therapeutics's statements, word for word
Compensation for this role includes base salary, annual discretionary bonus, long term incentive, 401(K) plan with employer contribution, health care and other insurance benefits (for employee and family), paid holidays, vacation, and sick days. A summary of our benefits can be found on our careers page.Celldex is proud to be an equal opportunity employer that strives to foster a culture of diversity, equity, and inclusion. We are committed to promoting a diverse environment through development, recruiting and community outreach.
Job intelligence
The context around this role
Live data · October 31, 2026
Salary intelligence
How the pay compares
This role's midpoint is 19% above the US median for Clinical Project Management roles at this level.
This roleEmployer provided
Manager roles in the US7 roles publishing pay
| Annual base pay | Low | Median | High |
|---|---|---|---|
| This role | $176,659 | — | $229,427 |
| All US (middle half) | $153,500 | $171,000 | $173,500 |
This role: Celldex Therapeutics's own published range. Comparisons: the base pay employers published on open Clinical Project Management roles at the same level on Regulatory Jobs, October 31, 2026. Nothing is estimated.
Career trajectory
Where this role sits in Clinical Project Management
The general path across 12 open Clinical Project Management roles on Regulatory Jobs, with the titles they carry most. Not Celldex Therapeutics's own promotion track.
Skills DNA
What this role leans on
How many of the posting's 26 duty, requirement and summary lines touch each area. The posting's emphasis, not a proficiency score.
- Clinical trial conduct7
- Collaboration and leadership7
- Documentation and SOPs2
- Quality systems and risk2
- GMP and compliance1
- Lab testing and methods1
- Regulatory submissions1
- Data and digital systems1
Regulatory intelligence
The rules behind this role
Frameworks and standards this posting's work falls under, matched from its own words, each linked to the official source.
Company hiring pulse
Celldex Therapeutics on Regulatory Jobs
- 8
- Open roles
- 8
- Distinct roles
- 3
- Locations
By discipline
- Quality5 63%
- Clinical3 38%
By level
- Director3 38%
- Associate & Specialist2 25%
- VP & Executive1 13%
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Global Clinical Project Leader at Celldex Therapeutics
Applications close May 22. $177K–$229K a year, employer provided.