Full-time
Clinical Project Manager I/Clinical Project Manager II/Senior Clinical Project Manager
Competitive
Entry, Mid, Senior LevelScience & PharmaceuticalPosted 26d ago
You'll complete your application on the employer's website.
← Back to jobs
Role overview
Job type
Salary
Competitive
Location
Sector
Posted
26 days ago
Job description
Clinical Project Manager I/Clinical Project Manager II/Senior Clinical Project Manager
Tags
81
GOOD MATCH
Experience Level
100
Skill
76
Industry Exp.
75
Clinical Trials
Pharmaceutical
Biotechnology
Healthcare
Responsibilities
Lead planning and execution of clinical trial projects from proposal through closeout
Act as primary sponsor liaison, ensuring alignment on scope, timelines, and deliverables
Develop and maintain project management and study plans
Coordinate cross-functional teams, vendors, and study stakeholders
Support protocol development, study documentation, and regulatory deliverables
Participate in feasibility, site selection, and bid defense activities
Oversee training plans and study team readiness
Benefits
Fully remote role (with occasional travel)
Symbio specializes in clinical research core services with a focus on dermatological product trials and research for FDA approvals.
Port Jefferson Station, New York, USA
https://symbioresearch.com
Growth Stage
Leadership Team
Debra Dow
COO
Recent News
Mexico Business
Stellantis Scraps Hydrogen Vans Over Cost, Low Demand
2025-07-19
Digital Journal
Stellantis pulls plug on hydrogen fuel cell vans
2025-07-17
Clean Technica
Stellantis Joins Growing List Of Hydrogen Mobility Retreats
2025-07-13
Company data provided by
AI Tools
Customize Your Resume
Maximize your interview chances
Build Cover Letter
Make your application stand out
Analyze How Well You Fit
Understand your strength & weakness
Qualifications
Bachelor's degree in Business Administration, Science, or related field (or equivalent experience)
3+ years in pharmaceutical and/or clinical research industry
2+ years in clinical project management
Demonstrated experience in managing low to moderate complexity trials
Strong knowledge of GCP, ICH guidelines, and clinical trial regulations
Excellent communication, time-management, and organization skills
Ability to manage multiple priorities in a fast-paced environment
Proficiency in Microsoft Office
Required skills
Clinical Project Management, Clinical Research, Clinical Practice (GCP), ICH Guidelines, Clinical Trial Regulations, Microsoft Office
Experience
3+ years
Interested in this role?
Apply directly on the employer's website — it only takes a few minutes.
Similar vacancies
Other roles in Entry, Mid, Senior Level or Science & Pharmaceutical
Prototyping Lab Technician, Robotics
Competitive
HealthcareFull-time
San FranciscoScience & PharmaceuticalsPosted 30+ Days Ago
You will work at the cutting edge of OpenAI's robotics hardware, partnering with hardware and software teams to develop, build, test, and iterate on robotic systems. Working closely with engineers, you will build prototypes, execute experiments, fabricate fixtures, troubleshoot hardware, and help drive rapid iteration…
HealthcareFull-time
USA - Torrance (205th Street)Science & PharmaceuticalPosted 25d ago
When you join us, you’ll be part of a global team harnessing the power of scientific testing and data-driven insights to build a healthier future. Clinical Research Coordinator Imagine your future with us At ALS, we encourage you to dream big.
Clinical Research Coordinator- Cardiac MRI Center
$21.64 - $26.50
HealthcareFull-time
BIDMC East CampusScience & PharmaceuticalPosted 26d ago
When you join the growing BILH team, you're not just taking a job, you’re making a difference in people’s lives. Responsible for screening research subjects for participation in clinical research projects, enrolling research subjects onto these studies, monitoring protocol implementation, completing required forms and reporting results.