Bicycle Therapeutics
VP, Head of Drug Safety & Pharmacovigilance
Bicycle Therapeutics, Cambridge, Massachusetts, us, 02140
VP, Head of Drug Safety & Pharmacovigilance
Full-time Contract type: Permanent 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, MA USA. 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. Reporting to the Chief Development Officer, the VP, Drug Safety & Pharmacovigilance will be responsible for leading the overall strategic direction for Safety and Pharmacovigilance and, through leadership of the team, oversee the operational delivery of safety and pharmacovigilance activities at Bicycle. You will be a highly experienced and visionary member of the Development Leadership Team and will actively contribute to the broader clinical development strategy. Key responsibilities Develop and implement a comprehensive drug safety & pharmacovigilance strategy aligned with Bicycle’s overall mission and goals. Collaborate with senior executives to integrate drug safety & pharmacovigilance considerations into overall business strategies, clinical development plans, and broader decision-making processes. Manage and lead the patient safety and pharmacovigilance function including oversight for activities, operations, and continued evolution toward a best-in-class organization. Accountable for ensuring that appropriate resources, systems, and processes are in place for the evaluation and reporting of safety information, and other responses, to meet applicable global regulatory requirements for all programs. Provide expert guidance and decision-making and help to shape the strategy and direction of the global function to meet the organizational needs and contribute toward the overall R&D strategy. Work with key stakeholders within the organization to develop safety and PV strategy for current products under development including proactively identifying and communicating emerging potential and/or urgent safety issues and to support signal detection and risk/benefit evaluation. Provide oversight of Serious Adverse Event (SAE) processing and ensure timely, compliant, and accurate safety reporting in accordance with applicable regulatory requirements, Good Clinical Practice (GCP), and standard operating procedures (SOP). Maintain expert knowledge of current ICH and health authority requirements, expectations, and trends in patient safety and pharmacovigilance, and ensure compliance in all activities. Ensure readiness for health authority inspections and partner audits, and represent Bicycle in inspections, audits, and other health authority meetings as required. Design, direct, and conduct ongoing safety surveillance of company drug products using internal and external resources to ensure delivery of high-quality pharmacovigilance services. Ensure risk management/reduction strategies are developed and included in relevant documents such as clinical study protocols. Represent Bicycle in interactions with regulatory agencies, industry consortia, and external stakeholders on drug safety matters. Monitor industry best practices and changes in global safety regulations and guidelines. Provide direction and leadership for departmental policies, SOPs, systems, communications, reporting (e.g., DSUR, PSUR, periodic line listings), and vendor selection/management to ensure global regulatory compliance. Minimum Qualifications Medical Doctor (MD/MBBS/DO) degree. Significant global drug safety/pharmacovigilance experience, including experience in developing systems and processes for handling, processing, analysis, and regulatory reporting of adverse event reports, including serious adverse events. Significant people leadership experience, proven track record of successfully leading, developing, and motivating teams. Exceptional ability to influence and inspire others, build strong relationships, and drive consensus across diverse stakeholders. Direct experience in interacting with regulatory authorities. Ability to formulate and articulate a clear and compelling vision for drug safety and PV that aligns with Bicycle’s long-term goals. Experience of taking an active leadership role within a development function, acting as a business leader (beyond solely representing Drug Safety/PV); collectively as a leadership team determining long-term strategic clinical development plans. Accustomed to influencing and interacting with Executive team and Board. Outstanding interpersonal and communication skills both written and oral and ability to communicate complex information clearly, succinctly, and persuasively. Effective skills directed toward driving collaboration, achieving results, influencing, and resolving conflicts across internal and external stakeholders. Demonstrated ability to thrive in a fast-paced, dynamic environment and manage multiple priorities effectively. Benefits Flexible working environment. Competitive reward including annual company bonus. Medical, dental, and vision insurance for eligible employees and their families with 100% of the premiums covered by the Company. Health and Dependent Care Flexible Spending Accounts. 401(k) plan with a 4% Company match and immediate vesting. Eligibility to accrue up to 23 paid time off days per full year worked, plus the option to buy up to 5 additional days. Employee assistance program. 10 Company holidays. Competitive Family Leave Policy. Eligibility for an option grant to subscribe to shares in Bicycle Therapeutics plc. 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.
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Full-time Contract type: Permanent 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, MA USA. 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. Reporting to the Chief Development Officer, the VP, Drug Safety & Pharmacovigilance will be responsible for leading the overall strategic direction for Safety and Pharmacovigilance and, through leadership of the team, oversee the operational delivery of safety and pharmacovigilance activities at Bicycle. You will be a highly experienced and visionary member of the Development Leadership Team and will actively contribute to the broader clinical development strategy. Key responsibilities Develop and implement a comprehensive drug safety & pharmacovigilance strategy aligned with Bicycle’s overall mission and goals. Collaborate with senior executives to integrate drug safety & pharmacovigilance considerations into overall business strategies, clinical development plans, and broader decision-making processes. Manage and lead the patient safety and pharmacovigilance function including oversight for activities, operations, and continued evolution toward a best-in-class organization. Accountable for ensuring that appropriate resources, systems, and processes are in place for the evaluation and reporting of safety information, and other responses, to meet applicable global regulatory requirements for all programs. Provide expert guidance and decision-making and help to shape the strategy and direction of the global function to meet the organizational needs and contribute toward the overall R&D strategy. Work with key stakeholders within the organization to develop safety and PV strategy for current products under development including proactively identifying and communicating emerging potential and/or urgent safety issues and to support signal detection and risk/benefit evaluation. Provide oversight of Serious Adverse Event (SAE) processing and ensure timely, compliant, and accurate safety reporting in accordance with applicable regulatory requirements, Good Clinical Practice (GCP), and standard operating procedures (SOP). Maintain expert knowledge of current ICH and health authority requirements, expectations, and trends in patient safety and pharmacovigilance, and ensure compliance in all activities. Ensure readiness for health authority inspections and partner audits, and represent Bicycle in inspections, audits, and other health authority meetings as required. Design, direct, and conduct ongoing safety surveillance of company drug products using internal and external resources to ensure delivery of high-quality pharmacovigilance services. Ensure risk management/reduction strategies are developed and included in relevant documents such as clinical study protocols. Represent Bicycle in interactions with regulatory agencies, industry consortia, and external stakeholders on drug safety matters. Monitor industry best practices and changes in global safety regulations and guidelines. Provide direction and leadership for departmental policies, SOPs, systems, communications, reporting (e.g., DSUR, PSUR, periodic line listings), and vendor selection/management to ensure global regulatory compliance. Minimum Qualifications Medical Doctor (MD/MBBS/DO) degree. Significant global drug safety/pharmacovigilance experience, including experience in developing systems and processes for handling, processing, analysis, and regulatory reporting of adverse event reports, including serious adverse events. Significant people leadership experience, proven track record of successfully leading, developing, and motivating teams. Exceptional ability to influence and inspire others, build strong relationships, and drive consensus across diverse stakeholders. Direct experience in interacting with regulatory authorities. Ability to formulate and articulate a clear and compelling vision for drug safety and PV that aligns with Bicycle’s long-term goals. Experience of taking an active leadership role within a development function, acting as a business leader (beyond solely representing Drug Safety/PV); collectively as a leadership team determining long-term strategic clinical development plans. Accustomed to influencing and interacting with Executive team and Board. Outstanding interpersonal and communication skills both written and oral and ability to communicate complex information clearly, succinctly, and persuasively. Effective skills directed toward driving collaboration, achieving results, influencing, and resolving conflicts across internal and external stakeholders. Demonstrated ability to thrive in a fast-paced, dynamic environment and manage multiple priorities effectively. Benefits Flexible working environment. Competitive reward including annual company bonus. Medical, dental, and vision insurance for eligible employees and their families with 100% of the premiums covered by the Company. Health and Dependent Care Flexible Spending Accounts. 401(k) plan with a 4% Company match and immediate vesting. Eligibility to accrue up to 23 paid time off days per full year worked, plus the option to buy up to 5 additional days. Employee assistance program. 10 Company holidays. Competitive Family Leave Policy. Eligibility for an option grant to subscribe to shares in Bicycle Therapeutics plc. 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.
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