Associate Director, Clinical Safety Scientist

2 weeks ago

Cambridge, Cambridgeshire, United Kingdom Bicycle Therapeutics Full time

Bicycle Therapeutics is a clinical-stage biopharmaceutical 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 BT8009, a Bicycle Toxin Conjugate (BTC) targeting Nectin-4, a well-validated tumor antigen; BT5528, a BTC 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 (BRCTM) for radiopharmaceutical use and, through various partnerships, is exploring the use of Bicycle technology to develop therapies for diseases beyond oncology.nBicycle Therapeutics is headquartered in Cambridge, UK, with many key functions and members of its leadership team located in Cambridge, MA.

nCulture

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

Adventurous . We believe it's the way to deliver extraordinary results for our patients.nWe are

Dedicated to our Mission . You can't change the world if you don't have determinationnWe are

One Team . We only succeed when we work together.

Job Description


The Drug Safety function within Bicycle Therapeutics provides clinical safety and pharmacovigilance support to medicines across life cycle.nReporting to the Head of Drug Safety, the Associate Director, Clinical Safety Scientist will lead the clinical safety activities for the assigned compounds within the organization.

Responsible for the implementation and the management of pharmacovigilance and risk management activities for assigned compounds in conjunction with the Company's development and planned commercial activities, industry standards, and compliance with global regulations.nYou will work with the Safety Lead to actively manage and evaluate risks associated with assigned projects and make recommendations for the management and communication of risks in accordance with global legal and regulatory frameworks.nKey ResponsibilitiesnDevelop and maintain an understanding of the safety profile of their assigned product(s) or therapy areas.nManage safety responsibilities on clinical study teams and provide input to clinical teams concerning safety aspects of the design and preparation of protocols, investigators brochures, informed consent forms and investigator notification letters.nSafety evaluation activities including First in Human (FIH) studies in collaboration with Safety lead, internal cross functional experts and external vendors.

Regular review of emerging safety data and timely presentation of important/urgent safety issues to the company senior management, other internal and external stakeholders (e.g Safety Monitoring Committee, Independent Data Safety Monitoring Boards)nResponsible for authoring and/or review of aggregate safety assessments and drug safety reports for signals/issues or in response to Regulatory Authority requests.nContribute to and summarize safety data effectively for use in regulatory or clinical trial documents (e.g.

ad-hoc queries, DSURs, PBRERs and RMPs).nResponsible for coordination and collaboration with external vendors servicing Bicycle Drug Safety; create/review Safety Management Plans (SMP) for the assigned projects and oversee clinical safety case management, aggregate reports and reconciliation for quality and compliance.nIn collaboration with external PV vendors and study Medical Monitor, review of MedDRA coding of AEs, assessment and follow up of SAEs including preparation of analyses of similar events (AOSE) for unexpected and related serious adverse events (SUSARs) from clinical trials.nContribute to regulatory authority submissions (New Drug Applications/NDAs, Marketing Authorization Applications/MAAs etc.) by reviewing safety data and preparing relevant sections of the filing and submission packages in consultation with Safety Lead and other cross functional colleagues.nAssist in preparation/update of safety related global SOPs to ensure the efficient operation of the drug safety function.

Qualifications

Relevant qualification within healthcare or Life Sciences or equivalent professional experiencenHave expertise and good knowledge of allphases from FIM to post approval and good working knowledge of relevant regulations (e.g. FDA, EU and ICH) and proven evidence of effective delivery of high quality documents.nHands-on understanding of the MedDRA and use of safety databases for adverse event evaluation and reportingnPrevious experience of managing clinical safety activities for multiple programmes and able to identify risks and propose corrective actions in complex and critical situationsnCuriosity and a solution driven approach to challengesnWillingness to challenge and be challenged to ensure optimal decision making and delivery of solutions for patientsnStrong work ethic, decision making skillsnExceptional teamwork skillsnAbility to work independently

Additional Information


State-of-the-art campus environmentwith on campus restaurant and Montessori nurserynFlexible working environmentnCompetitive reward including annual company bonusnEmployee recognition schemesn28 days annual leave in addition to bank holidays+ option to buy up to 5 additional days annuallynEmployer contribution to pension (employee does not have to contribute)nLife assurance cover 4x basic salarynPrivate Medical Insurance, including optical and dental cover.nGroup income protectionnEmployee assistance programnHealth Cash PlannAccess to company subsidized gym membership.nEligibility for an option grant to subscribe to shares in Bicycle Therapeutics plc.nCycle to work schemenBicycle 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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