Remote Medical Director, Clinical Development
Job
On-Board Companies
Remote
Full-Time
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Job Description
On-Board Services is hiring a Remote Medical Director, Clinical Development For immediate consideration please send your resume to resumes@onboardusa.com
Subject Line:
Position Title and State you are locatedAbout Us:
On-Board Services, Incorporated is an on-site contract service provider for a local manufacturing entity providing full time positions to our employees. We offer benefits as well as 401k.Position Details:
Title:
Medical Director, Clinical Development Position Type:
6 month contract with additional opportunity contingent upon performance and continued business needJob Location :
Remote Shift:
1st shiftBenefits :
401K, Dental insurance,Life Insurance, Medical Insurance, Vision Insurance, PTO Compensation :
$150-$166/HR Position Overview The Medical Director, Clinical Development partners closely with the Executive Director, Clinical Development, and is responsible for protocol design and scientific oversight of clinical research studies across new and marketed products. This role contributes to clinical development and regulatory strategy and is accountable for the design, execution, monitoring, and reporting of clinical trials. The position sits within the Global Clinical Development organization. Key Responsibilities Clinical Development & Study Execution Lead or support development and updates to global clinical development plans Design patient-centered clinical protocols aligned with strategic objectives and timelines Partner with Clinical Operations and vendors to identify and evaluate study sites Collaborate cross-functionally to address study challenges and ensure timely execution Provide clinical input into key study documents (protocols, informed consent forms, monitoring plans, statistical analysis plans, CRFs, etc.) Support and participate in Investigator Meetings Oversee study conduct to ensure data quality, protocol compliance, and efficient patient recruitment Partner with Biostatistics and Safety to interpret clinical data and contribute to Clinical Study Reports (CSRs) Medical Monitoring Provide oversight of CRO medical monitors to ensure patient safety and high-quality trial execution Review safety data and contribute to safety narratives and reports Regulatory Strategy Collaborate with Regulatory Affairs on global clinical and regulatory strategies Author and review regulatory documents, including briefing packages and submission dossiers External Engagement Contribute to publications, abstracts, and investigator-sponsored study (IIS) reviews Build relationships with key opinion leaders, patient advocacy groups, and cross-functional partners Support advisory boards and lifecycle management initiatives Participate in due diligence activities for external assets Qualifications Education MD, DO, or MRCP required Experience 4-6 years of clinical development experience in a biotech or pharmaceutical setting Relevant clinical experience in women's health, dermatology, or pediatrics preferred Candidates with strong clinical trial leadership or academic research experience will also be considered Skills Strong written and verbal communication skills Fluent in English (written and spoken) Proficient with Microsoft Office and common clinical/technical systems Willingness to travel as needed for clinical trials or external engagements Core Competencies Solid understanding of ICH, GCP, and clinical trial execution, including medical monitoring Ability to apply regulatory guidance, scientific literature, and therapeutic insights to inform strategy Strong analytical skills with the ability to interpret complex clinical data Collaborative mindset with experience leading cross-functional, matrixed teams Ability to work independently and manage competing priorities in a fast-paced environment High level of integrity and professional ethics www.onboardusa.com Apply Today! On-Board was founded in 1976 by Robert L. Wilson to provide Engineering and Design services to the chemical manufacturing industry. Today, On-Board is a thriving privately held family of companies with services including: Consulting, Professional Engineering, Industrial Maintenance and Facility Management, Contracted Manufacturing and Production Services, as well as Temporary Staffing and Recruiting throughout North America. The On-Board Family of Companies conducts operations through its Corporate Headquarters located in East Windsor, NJ along with Regional Offices in New Castle, DE and Wake Forest, NC. On-Board's Mission is to provide "Flexible Service by applying the talents of our people, work processes and technology to meet our clients' expectations in a Safe, Responsible and Dependable manner." On-Board Companies provides equal employment opportunities (EEO) to all employees and applicants for employment without regard to race, religion, sex, national origin, age, disability or genetics. JD# 25-00650 INDOJSimilar jobs in Jersey City, NJ
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