7 senior analyst jobs found in Waltham

Creative Circle Senior UX Designer (with Pharma/Life Sciences experience!) Location: Waltham, MA (West End neighborhood - not easily T accessible) On-Site Requirement: Hybrid - 3 days per week Duration & Hours: 6 months, 40 hours per week Rate Range: $50-$60 per hour (W2) Job Description: Our client, a digital engineering firm, is seeking a Senior UX Designer with to partner with their client based in Waltham, MA. This will be a long-term, hybrid Senior UX Designer role supporting a leading life sciences client in designing a next-generation internal portal for laboratory automation and drug discovery workflows. The role is 40 hours per week, onsite at least 3 days per week in Waltham, MA, and begins as a 6-month freelance contract with potential extension. You will lead user research, shape the information architecture and interaction design, and collaborate closely with cross-functional teams, including scientific staff, content leads, creatives, and a...

Alkermes, Inc. The Senior PV Scientist serves as a critical medical analytic and coordinating role in partnership with the Safety MD/Medical Monitor for assigned marketed and/or investigational product(s). The Senior PV Scientist is expected to be equally effective in working collaboratively or independently. She/he must demonstrate effective leadership skills with cross functional partners to ensure that signaling, safety data analyses/authorship for ad hoc queries and aggregate reports are of high quality and are completed and submitted according to required timelines. For investigational products, this role may also participate in protocol design, safety CRF development, safety monitoring plan, support of DSMB activities, coding review as well as SAE reconciliation activities. The Senior PV Scientist also plays a key role in ensuring that the above activities remain compliant with evolving regulations, that respective SOPs and work instructions regarding signaling, ad hoc and...

Alkermes, Inc. The Summer Intern will work closely with senior biostatisticians on statistical methodology and support for quantitative decision-making implementation in clinical trials. Full time summer internship lasts about 10-12 weeks. Starting time is flexible around May or June 2026. This can be a remote or hybrid internship onsite 3x a week in our Waltham, MA office. Basic Qualifications: Ph.D. candidate who has passed the qualifying exam in biostatistics, statistics, applied mathematics, or data sciences and is not expected to graduate prior to completion of the Summer 2026 internship. Have effective oral and written communication skills. Sufficient programming skills in SAS and/or R /or Python. Preferred Qualifications: Proficient in R and had experience of R Shiny in developing, testing and deploying dashboards about statistical metrics Be able to conduct literature review independently. Experience in the development and application of advanced...

Alkermes, Inc. The Summer Intern will work closely with senior biostatisticians on statistical methodology and support for quantitative decision-making implementation in clinical trials. Full time summer internship lasts about 10-12 weeks. Starting time is flexible around May or June 2026. This role can be remote or hybrid onsite 3x a week in our Waltham, MA office. Basic Qualifications: Ph.D. candidate who has passed the qualifying exam in biostatistics, statistics, applied mathematics, or data sciences and is not expected to graduate prior to completion of the Summer 2026 internship. Have effective oral and written communication skills. Sufficient programming skills in SAS and/or R /or Python. Preferred Qualifications: Proficient in R and had experience of R Shiny in developing, testing and deploying dashboards about statistical metrics Be able to conduct literature review independently. Experience in the development and application of advanced statistical...

Alkermes, Inc. In this leadership position, the Senior Director, Statistical Programming will serve as the head of statistical programming who oversees all statistical programming activities to support Alkermes' growing portfolio. This leader will provide guidance on statistical programming technical skills, selecting appropriate and innovative approaches to produce high quality deliverables for in-house and outsourced projects. This role will manage hiring, resource planning and setting strategic vision for the statistical programming group as well as assist on complex deliverables. This position is eligible for the hybrid workplace model, requiring work to be completed onsite at our Waltham, MA office at least 3 days per week. This role is not eligible for fully remote work Duties and Responsibilities: Develop and lead a team of high performing statistical programmers to meet corporate regulatory, scientific, and business objectives. Deliveries of the statistical...

Alkermes, Inc. Reporting directly to the Head of Medical Affairs, the VP, Head of Life Cycle Management (LCM) is a highly visible and business-critical role at Alkermes. This role is tasked with understanding the business strategies and drivers underlying our medicines for the treatment of serious mental illness, sleep disorders and our emerging neuroscience pipeline and translating those drivers into data generation plans across our programs and disease areas of interest. This individual will need to effectively collaborate and communicate with colleagues within Medical Affairs and key cross-functional partners (e.g., Commercial, Clinical Development, Clinical Operations, Regulatory Affairs, Safety, Biostatistics, Program Management, Government Affairs, Business Development), and frequently represent the function to senior management and the company to healthcare professionals. This position is based in Waltham, MA. Responsibilities Lead the efforts to collaborate with...

Alkermes, Inc. The Executive Medical Director serves as a senior member of the DSPV leadership team, accountable for the management, mentoring and development of assigned benefit-risk management staff as well as serving as a global safety officer for assigned investigational and/or marketed products. Reporting to the Head of DSPV, the Executive Director will also serve in a visible role in providing safety leadership and advisement in several company-wide forums and initiatives. The successful candidate will have demonstrated prior career success as a product safety physician and managing/ developing individuals and highly effective teams. This leader will be expected to roll-up their sleeves and help do the work in addition to managing direct reports. Key success factors also include building high trust, accountability and demonstrating a sense of urgency in leading critical projects, showing the capability to work either independently or collaboratively and to be able to...