Easter Seals Jobs

Our medical affairs physicians and scientists are experts on our medicines and form a valuable part of our global development organization. We serve as a significant liaison between Regeneron and the scientific and healthcare community. Medical Affairs is organized in an effectively aligned matrix structure for delivery of therapeutic and functional area expertise.

The Sr Mgr, Medical Affairs engages in scientific exchange and collaborates with therapeutic area experts on disease and product information as well as research initiatives. Participating in the development and management of company sponsored and investigator-initiated studies. Presenting scientific data, clinical data, and disease state awareness in response to requests for information to diverse audiences (therapeutic area experts, practitioners, investigators, research coordinators, site personnel and internal stakeholders).

This is a field-based position (covering Western Canada and based in Vancouver, BC area) and requires work in a multifunctional, matrix organization and possibly partner companies.

JOB DUTIES

• Identifies and maintains a list of relevant medical/therapeutic area experts, investigator targets and associated plans of action.

• Participates in the development and management of company sponsored clinical trials including:

• Review of concept proposals and development of protocols

• Identifies and assists in selection of investigators and trial sites

• Supports site initiation and enrollment activities

• Acts as a scientific resource for area health care professionals within the surrounding trial site community

• Collaborates with Clinical Development and other trial staff to execute plans and strategies established by Medical Affairs

• By establishing scientific relationship with investigators and internal Medical Affairs, supports investigator-initiated study (IIS) concept program.

• Identifies gaps in research needs of company and creates opportunities to fill those gaps by collaborating with potential and existing investigators and site personnel.

• Responds to requests for information related to study indications, disease state and therapeutic area, and presents/discusses scientific and clinical data to appropriate audience in a compliant manner.

• Performs disease management and therapeutic area education with identified practitioners, payers, and researchers.

• Attends medical conferences to collect and report relevant, scientific, clinical, & competitive intelligence with the purpose of informing internal collaborators.

• Assists with management of clinical data to ensure rapid and accurate communication of scientific/clinical results through support of abstract, poster, presentation, and manuscript development.

• Ensures company policies, procedures, principles, and financial controls are maintained with integrity and professionalism is displayed internally and externally

JOB REQUIREMENTS

• Healthcare professionals (PhD, PharmD, MD) possessing therapeutic experience and/or trial recruitment experience.

• 2 plus years of experience in a pharmaceutical industry or clinical setting such as drug information, disease management programs or clinical pharmacy/medicine.

• Track record of working corroboratively and developing relationships in academic and clinical practice settings

• Experience working in a matrix organization

• Travel is required for this role

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.