Data Collection Associate

CrossmarkBoston

On-site Part-time

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Experience Level

Entry Level

Qualifications

High attention to detail and accuracy in data entryStrong analytical skills and problem-solving abilitiesBasic knowledge of data management tools and softwareEffective communication skillsAbility to work independently and as part of a team

About the job

Join Crossmark as a Data Collection Associate in Boston, where your role will be pivotal in ensuring data accuracy and integrity. This part-time position is ideal for those looking to start their career in data management. You will be responsible for collecting, verifying, and entering data into our systems, contributing to our overall mission of providing exceptional service to our clients.

About Crossmark

Crossmark is a leading provider of sales and marketing services, known for our commitment to excellence and innovation. We empower our employees with the tools and training needed to succeed in a dynamic business environment.

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Data Collection Associate

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Part-time|On-site|Boston

Join Crossmark as a Data Collection Associate in Boston, where your role will be pivotal in ensuring data accuracy and integrity. This part-time position is ideal for those looking to start their career in data management. You will be responsible for collecting, verifying, and entering data into our systems, contributing to our overall mission of providing exceptional service to our clients.

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Senior Director of Global Regulatory Strategy - Regulatory Affairs

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Full-time|$275K/yr - $290K/yr|On-site|Boston, Massachusetts

At Olema Oncology, we are committed to pioneering advanced therapies for breast cancer and beyond. Our flagship program, palazestrant (OP-1250), is an innovative complete estrogen receptor antagonist (CERAN) currently undergoing development for metastatic breast cancer, showing significant promise as both a monotherapy and in combination therapy for ER+/HER2- metastatic breast cancer. Additionally, our next candidate, OP-3136, is a leading KAT6 inhibitor with potential to set new standards in treatment.Our scientific advancements are driven by an environment that encourages fearless support, motivation, and collaboration. At Olema, we believe that prioritizing our team leads to exceptional outcomes. If you are prepared to be part of something transformative, let’s collaborate to create meaningful impacts for our patients, your career, and the future of medicine.For more insights, view our latest corporate presentations here.About the Role: Senior Director, Global Regulatory Strategy Lead - Regulatory AffairsIn the position of Senior Director, Global Regulatory Strategy Lead - Regulatory Affairs, reporting to the Senior Vice President of Regulatory Affairs, your key responsibilities will include:Leading the development of the New Drug Application (NDA).Creating and implementing innovative regulatory strategies that support Olema's product portfolio.Acting as the subject matter expert for Regulatory Affairs on cross-functional teams, providing guidance to global project teams, Study Execution Teams, and the Executive Committee.Offering strategic and tactical oversight for the development of regulatory submissions, including INDs, CTx, briefing documents, IB, NDA, BLA, DMF, IMPD, etc.This role is based in either our Boston, MA or San Francisco, CA office and will involve domestic and international travel of up to 20%.This role will primarily involve:Leading the NDA development and submission for our lead programFormulating innovative global regulatory strategies for the Olema product suite, addressing both clinical development and lifecycle management as required.Representing Regulatory Affairs on cross-functional teams as the SME, delivering regulatory guidance and oversight to global project teams, Study Execution Teams, and the Executive Committee.

Mar 24, 2026

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Part-Time Retail Data Collection Associate

Crossmark

Part-time|On-site|Boston

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