Clinicaltrials Gov Jobs (NOW HIRING)

Support clinical trial programs and drug development legal review/creation (e.g., informed consent, ClinicalTrials.gov postings, FDA correspondence/submissions). * Counsel and train Marketing on ...

... Clinicaltrials.gov, EudraCT). The Associate Director is responsible for effectively partnering and engaging with internal (e.g., cross-functional study teams, senior management) and external key ...

Maintains accurate study registration (Clinicaltrials.gov, etc.). Maintains accurate study registration (Clinicaltrials.gov, etc.). * Research Operations - Administration 10% * Provides direction to ...

Oversee ClinicalTrials.gov listings and ensure all regulatory commitments and timelines are tracked and met. Submission Operations Oversee eCTD publishing and submission infrastructure, managing ...

Support clinical trial programs and drug development legal review/creation (e.g., informed consent, ClinicalTrials.gov postings, FDA correspondence/submissions). * Counsel and train Marketing on ...

... ClinicalTrials.gov, organizing and managing research data in Excel, and supporting a variety of ongoing research activities. We are looking for someone who is organized, curious, and eager to ...

... ClinicalTrials.gov) where relevant - in a clear, neutral format, always prioritizing the patient's best interest. • Coordinate the appropriate referral pathway based on patient preference ...

Identify and present potentially suitable study options -- including publicly listed alternatives (e.g., ClinicalTrials.gov) where relevant -- in a clear, neutral format, always prioritizing the ...

Other duties include reporting and registering clinical trials to the NCI's Clinical Trial reporting Program (CTRP) for accrual information and the clinicaltrials.gov registry for study outcome ...

... ClinicalTrials.gov and the EU Clinical Trial Register. Disclosures is also responsible for the EMA Policy 0070 (Publication of Clinical Data and Reports) activities. PROJECT INVOLVEMENT: Does not ...

... ClinicalTrials.gov and the EU Clinical Trial Register. Disclosures is also responsible for the EMA Policy 0070 (Publication of Clinical Data and Reports) activities. Project Involvement: Does not ...

Basic knowledge of clinicaltrials.gov, consenting, protocol review, adverse and serious adverse event reporting. * Ability to work independently, to make decisions, to interact with sponsors ...

Experience in use of online data sources and scientific/market databases (e.g., ClinicalTrials.gov, Cortellis, etc.) #LI-AS1 #LI-Onsite WHO WE ARE AND WHAT WE OFFER The expected salary range for this ...

Basic knowledge of clinicaltrials.gov, consenting, protocol review, adverse and serious adverse event reporting. * Ability to work independently, to make decisions, to interact with sponsors ...

Familiarity with PubMed, ClinicalTrials.gov, and other sources of clinical and scientific content * Experience in publication writing, including primary manuscripts, reviews, abstracts and poster ...

Basic knowledge of clinicaltrials.gov, consenting, protocol review, adverse and serious adverse event reporting. * Ability to work independently, to make decisions, to interact with sponsors ...

Familiarity with PubMed, ClinicalTrials.gov, and other sources of clinical and scientific content * Experience in publication writing, including primary manuscripts, reviews, abstracts and poster ...

Maintain and update clinicaltrials.gov, collaborate with biostatisticians to create statistical analysis plans; clean study data and create plans for data cleaning; analyze study data * Create data ...

Overview Black Canyon Consulting (BCC) is searching for a Quality Assurance Engineer to support the ClinicalTrials.gov (CTG) program at the National Institutes of Health (NIH) in Bethesda, MD. This ...

Maintain protocol development databases, ClinicalTrials.gov records, and internal tracking systems. * Plan and facilitate monthly disease committee teleconferences, prepare meeting agendas, generate ...