Mgr, Regulatory Intelligence
vor 7 Monaten
**Description**
**JOB SUMMARY**:
The Regulatory Intelligence Department at Syneos Health impact decision-making at the highest levels. The team translate and refine Syneos Health regulatory intelligence from internal and external sources and combine knowledge from therapy areas and functions to deliver proactive advice outlining risks and new opportunities to the regulatory strategy and operations.
**JOB RESPONSIBILITIES**:
- Ensures that clinical regulatory intelligence is collected and maintained in Syneos Health Regulatory Intelligence System (RIS):
- Ensures that the country specific regulatory requirements are current and accurate and available for services offered by Syneos Health for countries in which the organization operates or intends to operate in.
- Ensures that regulatory intelligence data is available in a standardized format within the Regulatory Intelligence System so that it can be used for project work, client consultation etc.
- Interacts with external and internal experts to collect country and region-specific regulatory intelligence.
- Work closely with Country SMEs contributing to the overall understanding of the local regulatory landscape.
- Conducts searches within commercial Regulatory Intelligence databases to identify regulations and guidelines relevant for clinical regulatory intelligence.
- Understands applicable local, national, and regional regulations and translates them into organizational best practices.
- Documents the interpretation in a standardized format within the Regulatory Intelligence System in line with implemented procedures and business needs.
- Reviews surveillance alerts and queries and determine actions to be taken through to implementation.
- Advises, consults, and makes final recommendations to all aspects of clinical regulatory intelligence.
- Makes recommendations in expertise to internal stakeholders.
- Keeps abreast of regulations, trends, developments, and advances in the global regulatory environment.
- Supports impact assessments of regulatory documents and guidelines on Syneos Health procedures as applicable and as assigned by management.
- Identifies and responds appropriately to issues and problems, providing innovative and effective solutions.
- Recommends and implements enhancements of Syneos Health Regulatory Intelligence processes to maintain the Regulatory Intelligence System
- Provides regulatory and technical training within the department and/or other departments/stakeholders, as required.
- May include line management responsibilities for staff members. For direct and indirect reports, may participate in and manage activities related to department staff operations.
- Timely and active participation and completion of all company and departmental requirements such as time reporting, meetings, performance reviews, etc.
- Other tasks as required
**Qualifications**
**QUALIFICATION REQUIREMENTS**
- BS degree or equivalent demonstrated experience in a relevant field
- Clinical research experience required including significant regulatory intelligence experience or regulatory affairs or regulatory operations, preferably from a clinical research organization.
- Good knowledge of country specific and regional regulations.
- Ability to analyze information across multiple sources and manage substantial amounts of details.
- Strong research skills required to support routine surveillance activities to detect, monitor, and synthesize complex regulatory information.
- Ability to react to internal and external changes, trends and development in the regulatory environment that may impact Syneos Health
- Knowledge of niche regulatory topics preferred.
- Excellent interpersonal and communication skills.
- Fluency in speaking, writing, and reading English.
- Exercises judgment within defined procedures and practices to determine proper action.
- Excellent customer service skills, with the ability to work both within teams and independently.
- Good people management, project management, problem-solving, and decision-making skills.
- Good initiative, adaptability, and pro-activity.
**Disclaimer**:
Tasks, duties, and responsibilities as listed in this job description are not exhaustive. The Company, at its sole discretion and with no prior notice, may assign other tasks, duties, and job responsibilities. Equivalent experience, skills, and/or education will also be considered so qualifications of incumbents may differ from those listed in the Job Description. The Company, at its sole discretion, will determine what constitutes as equivalent to the qualifications described above. Further, nothing contained here should be construed to create an employment contract. Occasionally, needed skills/experiences for jobs are expressed in brief terms. Any language held here is intended to fully follow all obligations imposed by the legislation of each country in which it works, including the implementation of the EU Equality Directive, in relation to the recruitmen
-
Associate Director, Regulatory Cmc
vor 2 Monaten
Home Office, Schweiz Apellis Pharmaceuticals Vollzeit**Position Summary**: We are looking for an** Associate Director, Regulatory Affairs Chemistry, Manufacturing, and Controls (CMC) **to join our team. We are expanding our existing group of exceptionally talented and well-motivated colleagues to provide regulatory CMC support for the development and commercialization of our products. This position will be...
-
Director, Regulatory Information Management
vor 6 Monaten
Home Office, Schweiz BeiGene VollzeitGeneral Description: The Director, RIM is responsible for partnering with internal and external stakeholders in executing the RIM strategy and vision for the organization. This includes activities related to RIM resources, planning and budgeting (in partnership with IT), for key systems implementation/upgrade, monitoring and analysis of submission and...
-
Principal Medical Writer
vor 6 Monaten
Home Office, Schweiz ICON VollzeitAs a Principal Medical Writer you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence. **What you will be doing**: - Develop regulatory documents for submission to regulatory agencies globally, including **Clinical Study Reports, Clinical Summaries of Efficacy and Safety, and...
-
Associate Clinical Science Development Director
vor 4 Monaten
Home Office, Schweiz Thermo Fisher Scientific Vollzeit**Work Schedule** Standard (Mon-Fri) **Environmental Conditions** Office **Position Overview** The Associate Director, Clinical Development Science provides clinical development expertise into a multi-disciplinary team engaged in advising clients in early through late-stage development of medical products. Inpout will be provided into the design and...
-
Cybersecurity Consultant
vor 6 Monaten
Home Office, Schweiz UNICC Vollzeit**Background information** The High Level Committee on Management (HLCM) of the UN formally adopted the Principles on Personal Data Protection and Privacy at its 36th Meeting on 11 October 2018. These principles set out a basic framework for processing “personal data”, defined as information relating to an identified or identifiable natural person, by...
-
Home Office, Schweiz International Telecommunication Union (ITU) VollzeitINTERNATIONAL TELECOMMUNICATION UNION - ITU is the leading United Nations agency for information and communication technologies, with the mission to connect the world. To achieve this, ITU manages the radio-frequency spectrum and satellite orbits at the international level, works to improve communication infrastructure in the developing world, and...
-
Project Manager
vor 7 Monaten
Home Office, Schweiz ICON VollzeitICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development. You will be joining one of our clients, a biotechnology company that is at the epicenter of...
-
Researcher
vor 6 Monaten
Home Office, Schweiz Freedom House Vollzeit**ABOUT FREEDOM HOUSE**: Established more than 80 years ago on the core conviction that freedom flourishes in democratic nations where governments are accountable to their people, Freedom House is a non-partisan, non-profit organization that works to defend and expand freedom globally to help secure a world where all are free. Around the world, repressive...
-
Medical Science Liaison
vor 6 Monaten
Home Office, Schweiz Argenx VollzeitJoin argenx At argenx, we build our culture from the collective power of the team and the knowledge that together, we are better. If you are entrepreneurial, curious and committed to make a difference for patients and thrive on creating solutions for rare autoimmune diseases, then argenx is for you. Next to a competitive salary with extensive benefits, we...