Regulatory Affairs Associate Consultant-plm

Are you interested in working directly for a single sponsor while having the security and additional career opportunities that working for a global CRO can bring? Our team says it's the best of both worlds.ClinChoice is searching for a **Regulatory Affairs Associate Consultant** to join one of our clients.**Main Job Tasks and Responsibilities**:- Accountable for reviewing new certificate requests and forwarding to relevant suppliers for processing- Responsible for NDA Annual Report compilation and Drug Listing submissions to FDA- Manages multiple tasks simultaneously to ensure performance metrics and filing deadlines are achieved according to agreed targets and BOH due dates.- Liaise with requester where necessary to collect the information needed to submit the certificate request to the Contractor. If re-work is identified, track all rework through client systems.- Forward request to the identified Contractor for processing, within the timeframes identified by the relevant project team.- If required, manage legalization through Consular Services ensuring relevant administration, fees are completed and timelines adhered to.- Communicate with requestor, Contractor or Consular Service to ensure request is processed, queries are answered and timelines are met.- Project manage multiple requests simultaneously, ensuring filing deadlines are reached and next action dates are maintained in real time by pulling pending reports from Client's systems.- Escalate to Client and Contractor point of contact when timelines may not be reached.- Maintain Client systems and process throughout processing of request to ensure real time reflection of request is visible to all users.- To seek approval from Client lead, should any certificates require fast tracking.- Supports delivery of electronic and paper regulatory transactions and electronic review aids in support of Drug Listings, Drug Establishment Registrations, And (A) NDA Annual Report submission to FDA- Continuous Improvement of selected processes relating to human health submissions and selected drug and non-drug specific projects and related activities e.g., Drug listing and Establishment registrations, Delivery of Product License Maintenance Portfolio in a timely and quality manner.**Education and Experience**:- Demonstrates ability to work within a demanding environment with a strong focus on quality and timelines.- Can demonstrate leadership and team skills.- Advanced Microsoft Office Suite skills.- Highly efficient communicator.- Acts decisively and seizes accountability- Bachelor's degree Level (desirable or equivalent work experience.- Familiarity with pharmaceutical organizational Structures.**The Application Process**:**Who will you be working for?****About ClinChoice**:ClinChoice is a global full-service CRO specializing in clinical development and functional solutions for pharmaceutical, biotechnology, medical device, and consumer health companies. We have over 28 years of proven high-quality delivery and results across all our services, with over 4,000 professionals in more than 20 countries across the Americas, Europe, and Asia-Pacific.**Our Company Ethos**:Our mission drives our culture: to contribute to a healthier and safer world by accelerating the development and commercialization of innovative drugs and devices. Our employees are the most valuable company asset and they are the fulcrum around which all ClinChoice activities are built and close management and training is the core instrument to develop and maintain highly-qualified personnel. The continuous training keeps the resources qualified in terms of competence and expertise and gives all personnel the clear tools needed to manage both internal and client processes with the same methodology. The success of these core values is evidenced by our below industry average turnover rates.ClinChoice is an equal opportunity employer. We have based our success on attracting, developing, and promoting talent guided by diversity and inclusivity. Our employees come from very diverse backgrounds: gender, race, beliefs, and ethnicities. We recognize this is our strength and celebrate it.**Key Words **:Regulatory Affairs, Regulatory Compliance, Regulatory Submission, Registrations, Product LicenseLI-PB1 #LI-REMOTE