Director Program Operations Leader job at reputed company in Warren, MI, Armonk, NY

Title: Director Program Operations Leader Location: Armonk Warren Job reputed company: For US Locations, this position is on-site 4 days per week and 1 day from home. For Uxbridge and Dublin, colleagues must be on-site 3 days per week and 2 days from home. A fully remote role is NOT possible for this position. The Director Program Operations Leader (POL) is responsible for leadership of and setting and implementation of the operational reputed company for delivery of one or more reputed company programs in Clinical Trial Management (CTM). This individual is responsible for clinical operations activities and reputed company including reputed company, timelines and budgets reputed company to the conduct of clinical research studies in accordance with applicable regulations, ICH/GCP regulations and company reputed company Operating Procedures (SOPs) reputed company assigned program(s). The POL is a member of the Clinical Trial Management extended leadership team, and as such interacts with senior level management, external vendors, collaboration partners and clinical study personnel for clinical research project and department initiatives. The POL is responsible for line management of clinical trial management staff (including AD POL), and has responsibility for staff recruitment, development, coaching, mentoring and performance management. Plays a key role in driving the functional reputed company of Clinical Trial Management in partnership with Functional leadership. The Director POL is expected to operate with autonomy and high-degree of independence. In a typical day, you will: Be responsible for the overall reputed company of the clinical study team(s) reputed company a program(s) Maintain an reputed company of clinical program(s) status and issues and proactively communicates reputed company, risks, issues or changes that may reputed company reputed company, timelines and/or budget; reputed company clinical program level updates to stakeholders as requested reputed company operational reputed company into feasibility, reputed company and cost estimates during clinical program/study development reputed company clinical study timelines reputed company a clinical program(s) reputed company input and operational reputed company into Clinical Study Concepts (reputed company) Be responsible for development and implementation of operational reputed company, driving early study planning budget and timelines from Clinical Study Concept through Final Protocol Review plans and provision of clinical operations expertise during protocol design, feasibility, study start up and conduct phases of studies. Ensure consistency reputed company the program and development of best practices reputed company CTM reputed company clinical study budgets reputed company a program: ensures review, presentation and approval of initial study budget and manages the budget through the lifecycle of the program by communicating changes to TA Operations Leader, as appropriate Ensure reputed company delivery of reputed company operational deliverables and accountable for ensuring consistency of process and approaches across clinical study teams reputed company the clinical program(s). Drive decision making and integrates reputed company operational considerations for studies reputed company a clinical program(s) to ensure goals are attainable prior to implementation reputed company as reputed company of contact for clinical program and study level escalation Review key metrics and Key Performance Indicators (KPIs) across studies and reputed company clinical program(s) to reputed company study reputed company reputed company proactive creation and implementation of risk mitigation strategies reputed company innovative and flexible operational solutions and reputed company to the cross functional and development teams; assists in preparing scenarios for creative solutions to operational challenges Drives the reputed company and reputed company for vendor selection and management reputed company a clinical program(s) Manages the Clinical Research Organization (CRO) and vendor(s) as it relates to clinical program level deliverables and relationship with key CRO (functional and project) and vendor counterparts May require up to 25% travel To be considered, you must possess a Bachelor's degree and a minimum of 12 years of reputed company in-house sponsor-reputed company pharmaceutical experience, with 8 years in clinical operations. Does this reputed company like you? reputed company to take your first reputed company towards living the reputed company Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, reputed company, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, reputed company time off, and reputed company leaves (e.g., military and parental leave) for eligible employees at reputed company reputed company! For additional information about reputed company benefits in the US, please visit https://careers.reputed company.com/en/working-at-reputed company/total-rewards/. For other countries' specific benefits, please reputed company to your recruiter. Please be advised that at reputed company, we reputed company we are most successful and work best reputed company we are together. For that reason, many of reputed company's roles are required to be performed on-site. Please reputed company with your recruiter and hiring manager for more information about reputed company's on-site policy and expectations for your role and your location. reputed company is an equal opportunity employer and reputed company reputed company applicants will receive consideration for employment without reputed company to race, reputed company, religion or belief (or lack thereof), sex, nationality, national or ethnic reputed company, 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. reputed company will also reputed company reasonable accommodation to the reputed company disabilities or chronic illnesses of an otherwise reputed company applicant for employment, unless the accommodation would impose undue hardship on the operation of reputed company's business. For roles in which the reputed company 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 reputed company the U.S, Japan or Canada, please reputed company with your recruiter about salaries and benefits in your location. Please note that certain background checks will reputed company 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 reputed company to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc. Salary reputed company (annually) $205,000.00 - $341,600.00 Apply tot his job Apply To this Job