Clinical Development Jobs in New Jersey
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Search Results - Clinical Development Jobs in New Jersey
The Carolan Group-Princeton (NJ)
Job Title: Executive Director, Clinical Development (Oncology)
Location: Princeton, NJ
Reports To: Chief Medical Officer / Senior Vice President of Clinical Development
Position Summary:
The Executive Director of Clinical Development in Oncology...
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Bridgewater (NJ)
into broader TPIP program strategy related to the pulmonary arterial hypertension indication in mid-to-late stage development. In addition, this role will be responsible for developing clinical strategic direction of engagements with health authorities related...
icims.com -
Piper Companies-Rahway
records for regulatory submissions (IND or CTA)Areas of focus will include biologics, vaccines, combination products, etc. Qualifications of the QA Specialist, Clinical Finished Goods2-5 years of quality assurance or clinical development experience...
RBW Consulting-Princeton (NJ)
groundbreaking antibody products that transform the lives of patients and the future of cancer treatment. This could be the next contract for you!
As Director, you will serve as a statistical expert supporting the clinical development of all compounds and report...
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Aequor Technologies LLC-Princeton (NJ)
for the development of high quality clinical documents submitted to Regulatory Authorities (e.g. FDA and EMA) including Clinical Study Reports, Investigator Brochures, Protocols, Protocol Amendments, Briefing Documents, Health Authority responses, and clinical summary...
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Randstad Life Sciences US-Bridgewater (NJ)
You will independently manage and coordinate complex drug development activities for cross functional development projects, including the project management of CMC, clinical and regulatory activities. You will also work across research, development...
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Katalyst Healthcares & Life Sciences-Bridgewater (NJ)
Responsibilities:
Supporting statistical programming activities for multiple and/or large/complex drug/vaccine clinical development projects.
Development and execution of statistical analysis and reporting deliverables (e.g. safety and efficacy...
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Merck Sharp & Dohme (MSD)-Trenton
GCS is accountable for the planning, sourcing, labeling, packaging and delivery of clinical supplies to clinical sites globally. The GCS Planning (Planning) organization is the key interface between clinical development teams and the operational...
1 similar job: Boston
Katalyst Healthcares & Life Sciences-South Plainfield
EST hours.
Requirements:
5+ years SAS programming experience
Knowledge of ADaM, SDDM, TLF, & SAS ODS Graphics.
Familiarity with CDISC standards for data structures.
Previous oncology experience and knowledge of clinical development process....
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Merck Sharp & Dohme (MSD)-Trenton
be located in West Point, PA, Rahway, NJ, San Francisco or Boston.As a director, you will serve as an expert QP2 representative on cross-functional teams of experienced scientists to discover and advance the clinical development of novel therapeutic agents...
1 similar job: Boston
eTeam-Parsippany
R&D Outsourcing within our Development Business Operations department. The Sr. Manager will have the opportunity to provide category management, sourcing and contracting expertise in clinical outsourcing of global Phase 1b-Phase 3 clinical trials...
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1 similar job: Foster City
Merck Sharp & Dohme (MSD)-Trenton
will serve as an expert QP2 representative on cross-functional teams of experienced scientists to discover and advance the clinical development of novel therapeutic agents for ophthalmologic disorders. You will work on the discovery and development of small...
1 similar job: Boston
Bridgewater (NJ)
Best Workplaces in New York™, PEOPLE® Companies That Care, Best Workplaces for Women™, Best Workplaces for Millennials™, and Best Medium Workplaces™ lists.
Overview: The role will be responsible for the oversight of the strategic clinical development...
icims.com -
The Fountain Group LLC-Basking Ridge
The individual assuming this role may function as a key member of the Global Product Team in collaboration with Clinical Development, Regulatory, Project Management, Biostatistics, Pharmacology, and other departments to strategically manage benefit-risk...
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Katalyst Healthcares & Life Sciences-South Plainfield
Responsibilities:
Responsible for supporting the Programming deliveries of a clinical study or project.
Implements statistical programming aspects of the protocol and the clinical development program.
Ensures high quality is built into own...
resume-library.com -
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