• Utilizing CSRs, prepare results from a number of therapeutic areas, in the Client Clinical Trial Results format, for submission to the EMA's results website, EudraCT.
• Circulate the prepared results for review by key clinical team members, addressing team questions, archiving the approvals and prepared result into the document repository.
• Prepare and make the submission in EudraCT.
• Assist the clinical disclosure team with any other support required for meeting the EU backlog of results submission to EudraCT or in facilitating clinical team review of redacted CSRs for voluntary data sharing.
Skills:
• Must have a minimum of 10 years clinical research and development experience, preparation of writing protocols, interpreting trial results and preparation of CSRs.
• Ability to influence and successfully work within complex cross divisional matrix across different cultures.
• Strong negotiation and conflict resolution skills;well organized, strong planning, tracking, problem solving and decision making skills.
• Minimum Bachelor degree in a scientific discipline required (chemistry, pharmacy, biology, etc.).
For more information, Please contact
Akriti Gupta
(973) 967-3409
Morristown, NJ 07960
Job details are sourced from the employer's original posting.
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Artech is an employer-of-choice for the last 25 years to over 7,500 consultants across the globe. We recruit top-notch talent for over 70 Fortune and Government clients coast-to-coast across the U.S., India, and China. We are #1 Largest Women-Owned IT Staffing Firm in the US and this may be your opportunity to join us! For more check: www.artechinfo.com