13 trial manager jobs at 8 companies in Heathrow, FL
2mo
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Daytona Clinical Research Positions (Pooling)
Daytona Beach, Florida, United States
OnsiteFull Time
Bachelor's degree; Master’s preferred; experience in clinical trials; knowledge of GCP/FDA guidelines; bilingual Spanish/English desirable; strong leadership and mentoring skills.
GCP, FDA regulations, clinical trial management systems, source documentation, phlebotomy, ECG
3w
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Director/Senior Director, Participant Recruitment & Engagement
Daytona Beach or United States
RemoteFull Time
Lead participant recruitment, engagement, and retention strategy for clinical trials; requires experience in recruitment/marketing, analytics, CRM/automation, stakeholder management, and team leadership.
2mo
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Clinical Research Coordinator / Project Manager
The Villages, Florida, United States
OnsiteFull Time
Coordinate clinical trials, adhere to protocols, collect patient data, knowledge of GCP/FDA guidelines; bilingual Spanish/English desirable; HS Diploma or GED required; Bachelor’s degree preferred; phlebotomy/LPN/RN preferred.
1d
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Clinical Research Site Development Manager/Senior CRC
Winter Park, Florida, United States
OnsiteFull Time
3+ YOERequires 3+ years of clinical research experience, trial acquisition, sponsor/CRO relationships, feasibility and site selection, study start-up, budget negotiation, regulatory knowledge, and GCP compliance.
FDA, IRB
1d
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Litigation Attorney
Orlando, Florida, United States
OnsiteFull Time
3+ YOERequires 3–5 years of civil litigation defense experience, case management, depositions, hearings, mediations, trial experience, strong research and writing skills, and Florida law practice licenses.
2mo
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Clinical Research Engagement Lead - South Region (Orlando, FL)
Orlando or South San Francisco
$109k-$202k/yr FieldFull Time
5+ YOEDegree in life sciences, 5+ years clinical research/operations experience, expert knowledge of ICH/GCP, site relationship management, experience with eTMF/Veeva and digital clinical trial tools, willingness to travel 30–50%.
Veeva, eTMF, eConsent, eSource, Remote Data Entry
2d
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Construction Litigation Attorney
Orlando, Florida, United States
OnsiteFull Time
10+ YOERequires 10–20 years of construction litigation experience, trial and dispute resolution experience, strong communication skills, and admission in good standing with the Florida Bar.
3mo
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Partner/Unit Lead - Employment Law
Orlando, Florida, United States
OnsiteFull Time
5+ YOEJuris Doctor and active Florida Bar membership, minimum 5 years employment law experience, litigation and leadership experience, client development and trial skills.
2mo
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Executive Director, Clinical Pharmacology Services Quality Assurance (United States or United Kingdom)
Madison or Dallas or Daytona Beach or Leeds
$220k-$245k/yr HybridFull Time
15+ YOEApproximately 15 years in clinical trials with senior QA/regulatory leadership; strong GCP and GMP expertise; bachelor’s in Life Sciences; global, matrixed leadership experience.
GCP, GMP, Quality Management System
3mo
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Partner/Unit Lead - General Liability
Orlando, Florida, United States
OnsiteFull Time
6+ YOEFlorida-licensed attorney with 6+ years in general liability litigation, partner-level responsibility, book of business, leadership and trial experience, strong communication and organizational skills.
1mo
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Gynecologic Oncology Leader -AdventHealth Orlando Cancer Institute
Orlando, Florida, United States
OnsiteFull Time
5+ YOEBoard-certified gynecologic oncologist with subspecialty training, minimum five years board-certified experience, ability to obtain Florida medical license, leadership in clinical trials and advanced robotic surgery experience.
1mo
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Gynecologic Oncology Leader -AdventHealth Orlando Cancer Institute
Orlando, Florida, United States
OnsiteFull Time
5+ YOEBoard-certified OB/GYN with gynecologic oncology subspecialty, minimum five years board-certified experience, leadership in clinical trials, advanced robotic surgery experience, and Florida medical license or ability to obtain.
1d
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Clinical Research Coordinator-Central Florida
Winter Park, Florida, United States
OnsiteFull Time
5+ YOERequires 5+ years of clinical research experience, sponsor/CRO relationship and trial acquisition experience, GCP/ICH knowledge, EDC platform experience, and independent leadership. Bachelor's degree, RN, or research certification preferred.
Medidata Rave, Veeva, Oracle, Electronic Data Capture (EDC), Good Clinical Practice (GCP), International Council for Harmonisation (ICH), Institutional Review Board (IRB)