At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections, where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally. This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come. Join Roche, where every voice matters.
The Department of Pharmacology and Toxicology is seeking an experienced individual with nonclinical business operations and outsourcing experience to support contracting and outsourcing of various non-GLP and GLP studies to Contract Research Organizations (CROs). The successful candidate will use their expertise to play an important role in the development of gene therapies and rapidly advance early assets through the pipeline. To this extent, the individual will effectively perform the duties of the outsourcing lead across the portfolio, but not limited to: outsourcing of studies, maintaining and managing CRO partners and relationships, tracking and forecasting budgets and timelines, and maintaining a master study schedule, etc.
Responsibilities
Manage outsourcing of preclinical studies (GLP and non-GLP) for inclusion in regulatory submissions, including but not limited to pharmacology, toxicology, and biodistribution studies.
Ability to on-board CROs, manage consultants and negotiate contracts on behalf of Spark.
Maintain and initiate relationships with established and new CROs based on business needs. Conduct feasibility assessments and participate in the selection of new CROs.
Generate and submit study designs to CROs, obtain competitive bids and timelines, and negotiate as appropriate.
Generate and manage CRO KPIs and governance as it relates to Spark needs. Track CRO issues and work with CROs to resolve them.
Participate in regular teleconferences with CROs including but not limited to: bi-weekly/monthly CRO program meetings, operational meeting, and governance
Effectively manage and track project timelines of nonclinical outsourced studies. Mange a Master Schedule.
Effectively manage budget across multiple departments as it relates to outsourced studies.
Facilitate discussions with CRO personnel and Spark SMEs as needed.
Manage CDC and CITIES permits. Track sample shipping and internal sample registries. Track animal procurement and pre-screening activities.
Effectively negotiate and facilitate open communication across all departments at Spark and maintain close relationship and communications with finance.
Independently support multiple programs with strong communication skills and ability to multitask.
Interface effectively with CMC and Supply Chain to manage test article supplies, orders and shipping.
Education and Experience Requirements
Complexity and Problem Solving
The expected salary range for this position based on the primary location of Pennsylvania is $112,600.00 - $209,200.00 USD Annual. Actual pay will be determined based on experience, qualifications, geographic location, and other job-related factors permitted by law. A discretionary annual bonus may be available based on individual and Company performance. This position also qualifies for the benefits detailed at the link provided below.
A healthier future drives us to innovate. Together, more than 100’000 employees across the globe are dedicated to advance science, ensuring everyone has access to healthcare today and for generations to come. Our efforts result in more than 26 million people treated with our medicines and over 30 billion tests conducted using our Diagnostics products. We empower each other to explore new possibilities, foster creativity, and keep our ambitions high, so we can deliver life-changing healthcare solutions that make a global impact.
Let’s build a healthier future, together.
Roche is an equal opportunity employer. It is our policy and practice to employ, promote, and otherwise treat any and all employees and applicants on the basis of merit, qualifications, and competence. The company's policy prohibits unlawful discrimination, including but not limited to, discrimination on the basis of Protected Veteran status, individuals with disabilities status, and consistent with all federal, state, or local laws.
If you have a disability and need an accommodation in relation to the online application process, please contact us by completing this form Accommodations for Applicants.
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At Roche, we believe that showing up as your authentic self is the key to innovation and collaboration. As the Associate Director of Nonclinical Outsourcing and Operations, you'll be integral to our mission of developing groundbreaking gene therapies and enhancing healthcare accessibility for future generations. Located in the vibrant city of Philadelphia, this role invites an experienced professional with a solid background in nonclinical business operations. You'll lead the outsourcing of GLP and non-GLP studies to Contract Research Organizations (CROs) while nurturing relationships with partners and ensuring all budget and timeline projections are met. Imagine playing a crucial part in managing essential studies like pharmacology and toxicology, and being the expert who navigates contractual negotiations and assesses feasibility with new CROs. If you’re detail-oriented and enjoy multitasking, this position offers a perfect blend of challenges and rewards. You'll effectively manage timelines, communicate with various departments, and ensure that all processes align smoothly with our overarching goals. With a Bachelor’s degree or higher and at least 15 years in the industry, you’ll bring a wealth of knowledge to this position. Embrace a culture that promotes creativity and collaboration, and be part of something truly transformative in healthcare.
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