Associate Director Clinical Scientist - Internal Medicine

We are seeking an Associate Director to join our Clinical Development team. The Associate Director Clinical Sciences leads in the development, evaluation, planning and execution of clinical studies. Ensures scientific integrity and interpretation of study data of a clinical development program. Leads in a matrix environment as part of a cross-functional team and may contribute to drug-candidate development projects through early and/or late phase development. Reports to the Internal Medicine Clinical Development Unit Lead of Clinical Scientists or Therapeutic area Lead Clinical Scientist and collaborates closely with Medical Director(s)to provide scientific expertise vital to design and deliver on clinical studies and programs.

As an Associate Director, a typical day may include the following:

May function as lead Clinical Scientist for program, and/or as delegate of Therapeutic area Lead Clinical Scientist; Member of the Clinical Study Team and Global Clinical Sub Team

Contributes to program team meetings, scientific advisory boards, study steering committees and data/safety monitoring meetings; may represent function in collaborative activities with other departments

Maintains proficient 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 drug landscape

Applies proficient scientific expertise to propose, design, and complete clinical research and development studies for early and/or late-stage assets; able to conceive and communicate strategy proposals well-grounded in supporting literature

Authors and/or reviews documents related to trials, such as medical monitoring plans, SAPs, informed consents and clinical components of the Clinical Study Reports with minimal guidance and supports the development of regulatory documents; performs quality review and/or approval; adjudicates and resolves cross functional comments with minimal support

Leads planning and prepares information for external /stakeholder meetings (IM, Governance, DMCs, Regulatory Authority); Presents data and information to external investigators (SIV) and internal collaborators

Performs clinical/medical data review, including safety monitoring and activities and procedures that ensure patient safety; Maintains compliance in accordance with FDA, EMEA, ICH and GCP guidelines as well as applicable SOPs regarding clinical safety

Promotes consistent first line medical/clinical data review techniques and conventions across studies/programs; Reviews clinical data review plan and authors medical monitoring plan for assigned studies/program

This role may be for you if:

Exhibit confidence and professional diplomacy, while effectively relating to people at all levels internally and externally; Demonstrated ability to Influence within team and department and may influence across functionally

Demonstrate initiative, creativity and innovation skills. Directly contributes to the development of innovations. Identifies opportunities to initiate operational changes

Strong cross-functional management, interpersonal and problem-solving skills; Considerable organizational awareness, including significant experience working cross-functionally

To be considered for this role, you must have a Bachelor's Degree, Advanced degree, or equivalent education/degree in life science/healthcare preferred (PhD/MD/PharmD/MSc). Additionally, we need 10 years of pharmaceutical clinical drug development experience. Experience in managing immune/inflammatory related clinical trials is preferred. Proven knowledge of the drug development process, Good Clinical Practice, study design, clinical research methodology & medical writing skills. We are looking for proficient knowledge of clinical development process, regulatory requirements and ICH/GCP guidelines.

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)

$173,500.00 - $283,100.00