Manager, Regulatory Affairs

Company Description

Bicycle Therapeutics is a clinical-stage pharmaceutical company developing a novel class of medicines, referred to as Bicycle molecules, for diseases that are underserved by existing therapeutics. Bicycle molecules are fully synthetic short peptides constrained with small molecule scaffolds to form two loops that stabilize their structural geometry. This constraint facilitates target binding with high affinity and selectivity, making Bicycle molecules attractive candidates for drug development. The company is evaluating zelenectide pevedotin (formerly BT8009), a Bicycle Toxin Conjugate (BTC) targeting Nectin-4, a well-validated tumor antigen; BT5528, a BTC molecule targeting EphA2, a historically undruggable target; and BT7480, a Bicycle Tumor-Targeted Immune Cell Agonist (Bicycle TICA) targeting Nectin-4 and agonizing CD137, in company-sponsored clinical trials. Additionally, the company is developing Bicycle Radio Conjugates (BRC) for radiopharmaceutical use and, through various partnerships, is exploring the use of Bicycle technology to develop therapies for diseases beyond oncology.

Bicycle Therapeutics is headquartered in Cambridge, UK, with many key functions and members of its leadership team located in Cambridge, Massachusetts US.

Culture is key and all Bicycle employees actively embrace and role model our company values:

• We are Adventurous. We believe it’s the way to deliver extraordinary results for our patients.
• We are Dedicated to our Mission. You can’t change the world if you don’t have determination.
• We are One Team. We only succeed when we work together.

Job Description

The Manager of Regulatory Affairs will be responsible for the development, execution and tracking of regulatory submissions for assigned BicycleTx programs or projects.

The Manager Regulatory Affairs may also be responsible for supporting the development of regulatory strategy and processes for their assigned BicycleTx programs or projects, working closely with cross-functional colleagues and senior members of the Regulatory Affairs team. As an integral member of the team that will be tasked with product development, the Manager Regulatory Affairs may also serve as a subject matter expert for assigned activities, which may involve multiple partners and collaborators, and will ensure adherence to relevant regulatory requirements.

• Responsible for the development and execution of global regulatory submissions for assigned BicycleTx programs or projects, including clinical trial applications
• Responsible for the maintenance of regulatory files and tracking databases, including relevant parts of the trial master file
• Collaborate with internal colleagues and external organizations to develop submission content plans and timelines and support the timely execution of regulatory submissions, responses to questions, audits and inspections
• May be responsible for the preparation, drafting, review, risk analysis and mitigation planning of submissions for assigned BicycleTx programs or projects, which may include selected key strategic submissions such as pediatric or orphan drug etc
• Developing and maintaining internal cross-functional relationships to support the development and execution of regulatory submissions for assigned BicycleTx programs or projects
• Supports the Global/Regional Regulatory Lead for assigned development programs
• May serve as primary contact with Health Authorities (HA) and/or external collaborators globally for assigned BicycleTx programs or projects.
• May support the development of processes, SOPs and other controlled documents, including for Regulatory Affairs activities
• Partners with Regulatory Affairs and cross-functional colleagues to understand the competitive landscape, e.g., views of HAs, regulatory precedents, labeling differences and therapeutic-specific issues and adapts to changes that may impact BicycleTx programs or projects
• Responsible for maintaining oversight of current and pending relevant regulatory approvals in therapeutic areas relevant to the assigned BicycleTx programs or projects
• Accountable for maintaining working knowledge of laws, guidances and requirements relevant to assigned BicycleTx programs or projects, in addition to general regulatory knowledge

Qualifications

• Bachelor’s degree in a scientific field or post-graduate degree preferred
• Demonstrable experience in Regulatory Affairs within the pharmaceutical or biotechnology industry; any in-depth experience may be limited to one specific region (e.g. US or EU)
• Working knowledge of FDA, EMA and ICH regulatory guidance and regulations
• Experience and knowledge in preparation of INDs, CTAs, or regional equivalents is desirable
• An understanding of the drug product lifecycle from discovery to clinical trials to marketing is required
• Experience and knowledge of some key regulatory pathways for product development, for example pediatrics, orphan drugs, is desirable
• Therapeutic experience in oncology is desirable
• Ability to communicate on topics of basic science is essential; a working knowledge of global drug development including preclinical & clinical is required
• Ability to proactively identify risks and develop risk mitigation strategies
• Adaptable with the ability to generate creative solutions, identify different and novel ways to find solutions, and adapt to changing priorities and deadlines.
• Collaborative, and able to build cross-functional relationships internally and externally
• Works proactively using solid communication and influencing skills to effectively execute program goals for assigned BicycleTx programs or projects
• Works effectively in a highly complex and fast-paced environment
• Strong organizational and time management skills
• Position may require limited domestic and international travel

Additional Information

• State-of-the-art campus environment with on campus restaurant and Montessori nursery
• Flexible working environment
• Competitive reward including annual company bonus
• Employee recognition schemes
• 28 days annual leave in addition to bank holidays + option to buy up to 5 additional days annually
• Employer contribution to pension (employee does not have to contribute)
• Life assurance cover 4x basic salary
• Private Medical Insurance, including optical and dental cover.
• Group income protection
• Employee assistance program
• Health Cash Plan
• Access to company subsidized gym membership.
• Eligibility for an option grant to subscribe to shares in Bicycle Therapeutics plc.
• Cycle to work scheme

Bicycle 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.