Clinical - Clinical Trials Disclosure Specialist
: Job Details :

Clinical Trials Disclosure SpecialistJob Number: 24-02719 Be part of a company that delivers life-changing healthcare solutions. ECLARO is looking for a Clinical Trials Disclosure Specialist for our client in Madison, NJ. ECLARO's client is a leader in the Biopharmaceutical Industry, providing quality, innovative, and affordable medicines that make a difference in the lives of patients all over the world. If you're up to the challenge, then take a chance at this rewarding opportunity! Position Overview: The Clinical Trial Disclosure Senior Specialist will provide the operational support of: Redaction of clinical trial documents in accordance with evolving global regulations. Key business partners are Clinical Development/Early Development Leads, Global Development Operations, Global Biostatisticians, Publications, Information Technology, Alliance Partners, Medical Writing, and Submission Managers. Responsibilities: Manage and Coordinate redaction of clinical documents in accordance with EMA Policy 0070, Health Canada Public Release of Clinical Information (PRCI), EU Clinical Trial Regulation, and other global regulations. Collaborate with Global Development Operations, Global Biostatisticians, Medical Writing, Submission Managers, and other stakeholders to operationalize redaction requirements Provide vendor oversight to support document redactions Work with IT, as needed, to implement technology solutions related to clinical trial disclosure Manage and track redaction book-of-work; compile and report on volume and performance metrics Provide operational support to CT Results Specialists, as required Assists in monitoring the global regulatory environment and maintains working knowledge of disclosure requirements Communicates with internal and external stakeholders to improve on processes and manage unmet need Trains new staff and develops job aids, work instructions, and user guides, as needed Qualifications: BA/BS or MA/MS in scientific or medical field 2-3 years of document redaction and 3+ years relevant work experience in a scientific or medical field with BA/BS Deep understanding of US/Canada and EU requirements for clinical trial disclosure as well as other related policies (ICMJE, PhRMA/EFPIA principles for responsible data sharing, etc.) Familiarity and comfortability working with and discussing scientific data Project and stakeholder management experience Demonstrated ability to work independently and seek out support when needed Exceptional written and oral communication skills Strong organizational skills with the ability to multitask and prioritize If hired, you will enjoy the following ECLARO Benefits: 401k Retirement Savings Plan administered by Merrill Lynch Commuter Check Pretax Commuter Benefits Eligibility to purchase Medical, Dental & Vision Insurance through ECLARO If interested, you may contact:Sofia Dela Torre...@eclaro.com(332) ###-#### Equal Opportunity Employer: ECLARO values diversity and does not discriminate based on Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status.