Senior Manager Regulatory Affairs CMC

The Senior Manager Regulatory Affairs CMC will be responsible for the development execution and tracking of CMC regulatory activities for assigned BicycleTx programs or projects.You will be responsible for supporting the development of CMC regulatory strategy and processes for their assigned BicycleTx programs or projects working closely with cross-functional colleagues and the Director Regulatory Affairs CMC. As an integral member of the team that will be tasked with CMC product development the Senior Manager Regulatory Affairs CMC will also serve as a subject matter expert (SME) for assigned activities which may involve multiple partners and collaborators and will ensure adherence to relevant regulatory requirements.Key ResponsibilitiesResponsible for the development and execution of regulatory strategy and submissions for assigned BicycleTx programs or projects with a focus on regulatory CMC including dossiers to support clinical trial applicationsResponsible for the regulatory assessment of change controls maintenance of regulatory files and tracking databases related to CMC submissionsCollaborate with internal colleagues and external organizations to develop submission content plans and timelines and support the timely execution of regulatory submissions that require CMC content responses to questions audits and inspectionsManage the preparation drafting review risk analysis and mitigation planning of CMC submissions (e.g. Module 3 IND IMPD amendments and annual reports) for assigned BicycleTx programs or projectsDeveloping and maintaining internal cross-functional relationships to support the development and execution of CMC regulatory submissions for assigned BicycleTx programs or projectsMay act as the Global/Regional CMC Regulatory Lead for assigned development programsMay support the development of processes SOPs and other controlled documents including for Regulatory Affairs activitiesPartners with Regulatory Affairs and cross-functional colleagues to understand the CMC regulatory landscape e.g. views of HAs regulatory precedents labeling differences and other CMC-specific issues and adapts to changes that may impact BicycleTx programs or projectsAccountable for maintaining working knowledge of CMC laws guidances and requirements relevant to assigned BicycleTx programs or projects in addition to general regulatory knowledgeThis is a hybrid working arrangement with a minimum of 1-2 days onsite from our Cambridge UK office.We are also open to those that can commit to a minimum of 0.8FTE (4 day week)We are only considering candidates who have a mix of CMC and Clinical Regulatory Affairs experience.Qualifications : Key Skills and CompetenciesBachelors degree in a scientific field or post-graduate degree preferredStrong demonstrable experience in CMC Regulatory Affairs within the pharmaceutical or biotechnology industry; particularly relating to peptides and drug-conjugates; any in-depth experience may be limited to one specific region (e.g. US or EU).General clinical regulatory experience supporting global clinical trial applications (not limited to CMC) is essential.Working knowledge of FDA EMA ICH and cGMP CMC regulatory guidance and regulationsExperience and knowledge in preparation of CMC sections of INDs CTAs NDAs MAAs or regional equivalents is requiredExperience and knowledge in the supportive interactions with health authorities including US FDA EMA and/or EU Member States is desirableAn understanding of the drug product lifecycle from discovery to clinical trials to marketing is requiredAbility to communicate on topics of basic science is essential; a working knowledge of global drug product development is requiredAbility to proactively identify risks and develop risk mitigation strategiesAdaptable with the ability to generate creative solutions identify different and novel ways to find solutions and adapt to changing priorities and deadlines.Highly collaborative strong relationship building skills with internal and external partners with a high level of integrityWorks proactively using solid communication and influencing skills to effectively execute program goals for assigned BicycleTx programs or projectsWorks effectively in a highly complex and fast-paced environmentStrong organisational and time management skillsPosition may require some domestic and international travel                Additional Information : State-of-the-art campus environmentCompetitive reward including annual company bonus28 days annual leave in addition to bank holidaysEmployer contribution to pension (employee does not have to contribute)Life assurance cover 4x basic salaryPrivate Medical Insurance including optical and dental coverHealth Cash PlanEligibility for an option grant to subscribe to shares in Bicycle Therapeutics plc.Cycle to work schemeBicycle Therapeutics is committed to building a diverse workforce that is representative of the communities we serve. We recognize that diverse and inclusive teams build a stronger and more innovative company. Therefore all qualified applicants will be considered for employment and we do not discriminate on the basis of race religion colour gender sexual orientation age disability status marital status or veteran status.Remote Work : NoEmployment Type : Full-time Key Skills Proofreading,Adobe Acrobat,FDA Regulations,Manufacturing & Controls,Biotechnology,Clinical Trials,Research & Development,GLP,cGMP,Product Development,Chemistry,Writing Skills Experience: years Vacancy: 1