Insmed is a global biopharmaceutical company on a mission to transform the lives of patients living with serious and rare diseases. Our most valuable resource is our employees, and everything we do is motivated by a patients-first mentality. We are dedicated to growing our team with talented individuals from around the world who are willing to challenge the status quo, solve problems, and work collaboratively with a sense of urgency and compassion.

Guided by our core values of collaboration, accountability, passion, respect, and integrity, we aim to foster an inclusive, diverse, and flexible work environment, where our employees are recognized for leaning in and rolling up their sleeves. If you share our vision and want to work with the most dedicated people in the biopharma industry, come to Insmed to accelerate your career.

 

	Consistently Ranked Science’s Top Employer Insmed is dedicated to creating a collaborative environment where our team can thrive. Every day, our employees turn their passion for science and research into innovative solutions for patients. That’s why we’ve been named the No. 1 company to work for in the biopharma industry in Science’s Top Employers survey for four years in a row.

 

A Certified Great Place to Work® We believe our company is truly special, and our employees agree. In July 2024, we became Great Place to Work-certified in the U.S. for the fourth year in a row. We are also honored to have been listed on the Best Workplaces in Biopharma™, Best Workplaces in New York™, PEOPLE® Companies That Care, Best Workplaces for Women™, Best Workplaces for Millennials™, and Best Medium Workplaces™ lists.

 

The Sr Manager, Clinical Programming will provide clinical programming support to multiple clinical studies and submissions. As a senior member of the Programming function, the Sr Manager, Clinical Programming will be working interactively with functional colleagues from Biostatistics, Data Management, Clinical Trial Operations, and Clinical Development, as well as external vendors.

Responsibilities (Essential Role Responsibilities):•    Leads the clinical programming activities and related oversight activities ensuring quality and timeliness across multiple studies
•    Sets tasks, prioritization, and resources for clinical programming on assigned studies
•    Provides hands-on programming support to clinical programming activities, both internally and in response to regulatory agencies’ requests for information as needed
•    Ensures quality of deliverables by consistently applying analysis and reporting standards, and driving compliance with regulatory requirements, corporate and departmental SOPs and Work Instructions
•    Leads process improvement initiatives
•    Motivates and mentors Managers and Sr Programmers to complete assigned deliverables on time and with high quality
•    Leads non project initiatives and utilizes resources to meet corporate objectives
•    Provides review and/or authors SOPs and/or Work Instructions related to clinical programming practices
•    Ensures creation of specifications for data transformation in accordance with SDTM IG and SAP
•    Creates CDISC compliant deliverables - SDTM datasets and annotated eCRFs (aCRF) or ensures the quality of these deliverables produced by a vendor
•    Works with clinical development teams to ensure the creation of medical monitoring reports, data cleaning reports, data reconciliation reports, and data visualizations as needed
•    Ensures professional development to enhance knowledge, skills, communication, scientific methodology, operational efficiency, and compliance with policies, regulations, and corporate standards and processes
 Position Requirements (Required and/or Preferred Skills, Experience and Education):•    Requires a Bachelor’s degree or higher in Statistics, Computer Science, Mathematics, Engineering or related field of study
•    Master’s degree or higher in Statistics, Computer Science, Mathematics, Engineering or related field of study is a plus
•    Minimum 6-7 years of work experience in a pharmaceutical/biotech (preferred) or related industry
•    Solid programming background and advanced SAS, R, or Python programming skills required. 
•    Significant knowledge of data visualization tools (e.g., JReview) is required
•    Strong experience in clinical programming with an understanding of data management
•    Prior submission experience is a plus
•    Prior experience in line management (direct reports) is a plus
•    CDISC experience in SDTM standards is required
•    Must have excellent communication skills (verbal and written)!
•    Highly organized with a strong attention to detail, clarity, accuracy, and conciseness
•    Individuals must demonstrate the ability to interact successfully in a dynamic and culturally diverse workplace!

119000-167267

At Insmed, we’re committed to investing in every team member’s total well-being, now and in the future. Our benefit programs vary by country but we offer the following to all Insmed team members, regardless of geographic location:

• Flexible approach to how we work
• Health benefits and time-off plans
• Competitive compensation package, including bonus 
• Equity Awards (Long-Term Incentives)
• Employee Stock Purchase Plan (ESPP)

 

For more information on U.S. benefits click here.

 

 

Insmed Incorporated is an Equal Opportunity employer. We do not discriminate in hiring on the basis of physical or mental disability, protected veteran status, or any other characteristic protected by federal, state, or local law. All qualified applicants will receive consideration for employment without regard to sex, gender identity, sexual orientation, race, color, religion, national origin, disability, protected Veteran status, age, or any other characteristic protected by law.

 

Unsolicited resumes from agencies should not be forwarded to Insmed. Insmed will not be responsible for any fees arising from the use of resumes through this source. Insmed will only pay a fee to agencies if a formal agreement between Insmed and the agency has been established. The Human Resources department is responsible for all recruitment activities; please contact us directly to be considered for a formal agreement.

 

Insmed is committed to providing access, equal opportunity, and reasonable accommodation for individuals with disabilities in employment, its services, programs, and activities. To request reasonable accommodation to participate in the job application or interview process, please contact us by email at TotalRewards@insmed.com and let us know the nature of your request and your contact information. Requests for accommodation will be considered on a case-by-case basis. Please note that only inquiries concerning a request for reasonable accommodation will be responded to from this email address.

 

Applications are accepted for 5 calendar days from the date posted or until the position is filled.