Associate Director, Clinical Operations
Candel Therapeutics —Remote
- $170,000 - $215,000 a year
- Full-time
- Hybrid work
- Management
- 8 years
- Bachelor's degree
Clinical Scientist Associate Director – Cardiovascular Trials
Amgen —Remote
- $169,793.45 - $229,720.55 a year
- Remote
- Doctoral degree
- 3 years
- Master's degree
- Disability insurance
- Health insurance
Associate Director, Clinical Quality Assurance Auditor
Cytokinetics —Remote
- $195,300 - $227,850 a year
- Full-time
- Remote
- Bachelor's degree
- Travel
- Senior level
Associate Director, Clinical Pharmacology
Nektar Therapeutics —Remote
- $185,000 - $220,000 a year
- 5 years
- Bachelor's degree
- Doctor of Philosophy
- Employee stock purchase plan
- Paid holidays
Statistical Programming Associate Director
Sumitomo Pharma America, Inc. —Marlborough, MA
- $168,000 - $210,000 a year
- Full-time
- Bachelor of Science
- Pass drug screening
- Office
- Paid holidays
- Health insurance
Associate Scientific Director, Clinical Pharmacology
Biogen —Remote
- $144,000 - $240,000 a year
- Full-time
- 5 years
- Doctor of Philosophy
- Senior level
- Paid parental leave
- Employee stock purchase plan
Clinical SAS Programmer
Katalyst Healthcares & Life Sciences —Newark, NJ
- Multiple hires
- Computer Science
- Bachelor of Science
- Writing skills
Quick Apply
Associate Director, Agios Clinical Educator, Sickle Cell Disease (East Zone)
Agios Pharmaceuticals —Remote
- $153,541 - $230,312 a year
- 3 years
- Bachelor's degree
- Travel
- Health insurance
Associate Director, Statistical Programming
Amylyx Pharmaceuticals —Cambridge, MA
- $188,000 - $211,000 a year
- Computer science
- 6 years
- Computer Science
12d
Associate Medical Director
Camarena Health —Madera, CA
- $300,000 - $350,000 a year
- Full-time
- Medicine
- Writing skills
- HIPAA
- Health insurance
- Dental insurance
Quick Apply
Medical Director
Bethel Family Clinic Inc. —Bethel, AK
- $175,000 - $250,000 a year
- Full-time
- Background check
- Nursing
- Medicine
- Loan repayment program
- Relocation assistance
Quick Apply
DIRECTOR OF REHABILITATION
Harrogate village —Lakewood, NJ
- $115,000 - $120,000 a year
- Skilled nursing facility
- Physical & Rehabilitation Medicine
- Physical Therapy License
- AD&D insurance
- Disability insurance
Quick Apply
Program Director — Detox & Outpatient Services
Sequoia Detox Centers —Spokane Valley, WA
- $92,500 - $100,000 a year
- Full-time
- Background check
- LMFT
- Nursing
- Continuing education credits
- Paid holidays
Quick Apply
BCBA Clinical Supervisor
Alongside ABA —San Fernando, CA
- $85,000 - $95,000 a year
- Full-time
- School experience
- HIPAA
- Clinic experience
- Continuing education credits
- Paid holidays
Quick Apply
Regional Director – Clinical Programming - as LCSW, LMFT, LPCC, or PsyD (Travel Required)
Alamo Health Management of Santa Clarita —Newhall, CA
- $150,000 - $170,000 a year
- 8 hour shift
- Background check
- LMFT
- Up to 50% travel
- Health insurance
- Dental insurance
Quick Apply
Board Certified Behavior Analyst (BCBA)
Cultivate Behavioral Health & Education —Keller, TX
- $80,000 - $90,000 a year
- Full-time
- Applied behavior analysis
- Pass drug screening
- Mid-level
- Paid holidays
- Health insurance
Quick Apply
Postdoctoral Research Fellow - McWilliams School of Biomedical Informatics
UTHealth Houston —Houston, TX
- Analysis skills
- University
- Doctor of Philosophy
- Health insurance
- Employee discount
Director of Nursing
ADDICTION AND MENTAL HEALTH SERVICES, LLC —Lafayette, TN
- Full-time
- Nursing
- Inpatient
- Residential
- Loan repayment program
- Health insurance
On-Site Clinic Director - (BCBA) Competitive Pay & Great Benefits!
BridgeCare ABA —Charlotte, NC
- Up to $120,000 a year
- Full-time
- Working with individuals with developmental disabilities
- Applied behavior analysis
- Clinic experience
- Health insurance
- Dental insurance
Quick Apply
10d
Associate Creative Director - Copy
Simons-Michelson-Zieve, Inc. Advertising (SMZ) —Troy, MI
- Full-time
- Hybrid work
- Management
- Office
- 8 years
- Health insurance
- Dental insurance

I want to receive the latest job alert for Associate Director, Clinical Programming

By signing in to your account, you agree to SimplyHired's Terms of Service and consent to our Cookie and Privacy Policy.

Explore jobs in more locations

Associate Director, Clinical Programming jobs near

Associate Director, Clinical Operations

Candel Therapeutics -
Remote

Apply Now

Job Details

Full-time
$170,000 - $215,000 a year

Qualifications

Bachelor's degree

Full Job Description

Associate Director, Clinical Operations

Location

Open to remote setting if willing to travel to Needham,MA office about 1x a quarter

Compensation

$170,000–$215,000 salary + annual bonus + options

Why Work With Us?

At Candel, our people drive our success. We value diversity, collaboration, and bold thinking in a supportive, mission-driven environment. Like a team, we show up for each other and stay focused on making a difference for patients and families. Our leadership is transparent and empowering, and our culture is built on trust, flexibility, and accountability, encouraging ownership and innovation every day.

Our Science: Advancing Cancer Immunotherapies

Candel is a clinical-stage biopharma company developing off-the-shelf, multimodal immunotherapies that stimulate personalized, systemic anti-tumor responses. Our platforms use genetically modified adenovirus and HSV constructs. With positive Phase 3 results for our lead candidate, it’s an exciting time to join us and help bring transformative cancer treatments to patients.

Learn more: www.candeltx.com

Functional Area

Clinical Operations

Reports To

Vice President, Clinical Operations or delegate

Position Summary

We’re looking for an Associate Director, Clinical Operations to lead execution of global oncology clinical studies with strategic oversight, operational excellence, and a collaborative leadership style. This is a highly visible role responsible for end-to-end operational strategy and execution of one or more Phase 2 and Phase 3 oncology trials.

You’ll work closely with cross-functional teams, CROs, vendors, clinical sites, and internal stakeholders to ensure studies are delivered on time, within budget, and with the highest quality standards.

This role is ideal for someone who thrives in a fast-paced biotech environment, can independently lead complex global studies, proactively solve problems, and confidently navigate ambiguity while remaining hands-on and team-oriented.

What You’ll Do

Lead operational planning and execution of assigned clinical studies, ensuring alignment with development timelines and program objectives
Provide strategic oversight and leadership to cross-functional study teams including CTMs, CTAs, CRAs, vendors, and CRO partners
Coordinate study execution from startup through database lock and closeout including site activation, enrollment tracking, monitoring oversight, and issue escalation
Partner closely with CROs and external vendors to ensure adherence to project timelines, scope, quality expectations, and budget
Monitor study progress and proactively identify operational risks, implementing mitigation strategies to support successful trial execution
Conduct co-monitoring visits as needed and support oversight of CRAs and site performance
Contribute to development and review of study protocols, amendments, informed consent forms, CRFs, study manuals, and operational plans
Support inspection readiness activities including risk assessments, audit preparation, and serving as an operational lead during regulatory inspections
Partner with Clinical Operations leadership on study budgets, accrual forecasting, invoice review, and financial tracking
Drive continuous improvement initiatives through SOP development, process optimization, and implementation of operational best practices
Mentor and support junior team members while contributing to a collaborative and accountable team culture

What You Bring

Bachelor’s degree in a scientific, medical, or healthcare-related discipline required; advanced degree preferred
Approximately 8+ years of progressive experience in clinical trial operations
Recent experience independently managing complex Phase 2 and Phase 3 oncology clinical trials
Strong understanding of ICH-GCP guidelines and global regulatory requirements governing clinical research
Experience overseeing CROs, external vendors, and global study execution in a biotech or pharmaceutical environment
Proven ability to manage operational complexity while remaining hands-on and solutions-oriented
Strong organizational skills with the ability to manage multiple priorities in a fast-paced environment
Excellent written, verbal, and cross-functional communication skills
Experience participating in regulatory inspections and inspection readiness activities preferred
Experience mentoring or guiding junior team members preferred
High emotional intelligence, strong collaboration skills, and a humble, team-first mindset

Why You’ll Succeed at Candel

You know how to lead through complexity while remaining calm, organized, and proactive
You’re comfortable rolling up your sleeves and stepping into hands-on operational challenges when needed
You thrive in lean, fast-moving biotech environments where visibility and ownership are high
You value collaboration, transparency, accountability, and continuous improvement
You care deeply about patients, science, and building strong relationships across teams

Work Environment

This is a hybrid position based in the Greater Boston area. Onsite presence is expected several days per week based on business needs and cross-functional collaboration.

Occasional domestic travel (~20%) may be required for site visits, co-monitoring, inspections, or investigator meetings.

Additional Information

Must be authorized to work in the United States. We are unable to accommodate sponsorship now or in the future.

NOTE: We are not currently partnering with external agencies for this search. We kindly ask that agencies refrain from direct outreach regarding candidate submissions or recruiting services.

elWri84YEb

Apply Now

Refine Your Search

Associate Director, Clinical Programming jobs

I want to receive the latest job alert for Associate Director, Clinical Programming

Related Searches

Explore jobs in more locations

Associate Director, Clinical Operations

Location

Compensation

Why Work With Us?

Our Science: Advancing Cancer Immunotherapies

Functional Area

Reports To

Position Summary

What You’ll Do

What You Bring

Why You’ll Succeed at Candel

Work Environment

Additional Information