Associate Manager, Clinical Scientist, Oncology

As a Manager in Clinical Sciences, Oncology, you will assist in the development, evaluation, planning and execution of clinical studies. Additionally, ensures scientific integrity and interpretation of study data of a clinical development program. You will work in a highly collaborative, matrixed environment as part of a cross-functional team and may contribute to candidate development projects through early and/or late phase development. Reports to the Senior Director, Clinical Sciences and collaborates closely with Medical Director(s) (MDs) to provide scientific expertise vital to design and deliver on clinical studies and programs.

As a Manager in Oncology Clinical Sciences, a typical day may include the following:

• Contribute to program team meetings, scientific advisory boards, study steering committees and data/safety monitoring meetings; participates in collaborative activities with other departments; Member of the Clinical Study Team and the Global Clinical Sub-Team
• Develops/maintains understanding of therapeutic disease area(s) and drug candidate including underlying disease biology, clinical manifestations and therapeutic standard practice, compound(s) including mechanism of action and limited knowledge of disease and drug landscape
• Applies basic scientific expertise to support execution of clinical research and development studies for early and/or late stage assets
• May assist with preparation of documents related to trials, such as medical monitoring plans, SAPs, informed consents, clinical components of the Clinical Study Reports and regulatory documents; collaborates with others for scientific and foundational guidance
• Maintains compliance in accordance with FDA, EMEA, ICH and GCP guidelines as well as applicable SOPs regarding clinical safety
• May contribute to preparations for external /stakeholder meetings (IM, Governance, DMCs, Regulatory Authority)
• Supports clinical/medical data review, including safety monitoring and activities and procedures that ensure patient safety; Supports identification of data trends and potential inconsistencies in data across assigned studies and raises appropriately
• Exhibits basic research and analytical knowledge to understand how study objectives and design impact data analysis; supports identification of critical risks and mitigations to study
  
  

This Role May Be For You If

• Demonstrated ability to influence and share new insights with study team
• Independently resolves most issues and complex matters, requiring sophisticated analytical skill, training and/or education. Raises highly complex problems or out-of-policy issues
• Strong management, interpersonal and problem-solving skills
  
  

To be considered for this role, you must have a Bachelor’s Degree required or Advanced degree or equivalent education/degree in life science/healthcare preferred (PhD/MD/PharmD/MSc). We are seeking≥ 5 years of pharmaceutical clinical drug development experience. Proven knowledge of the drug development process, Good Clinical Practice, study design and clinical research methodology; beginner level medical writing skills. We are seeking a knowledge of the clinical development process, regulatory requirements and ICH/GCP guidelines. Proven track record in clinical trial process improvements. Considerable organizational awareness, including significant experience working cross-functionally.

Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive and diverse culture that provides comprehensive benefits, which often include (depending on location) health and wellness programs, fitness centers, equity awards, annual bonuses, and paid time off for eligible employees at all levels!

Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.

For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.

Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.

Salary Range (annually)

$124,200.00 - $202,800.00