Source Job

• Lead cross-functional teams to execute commercialization launch of new or modified products.
• Actively communicate critical launch milestones and timelines to meet 1st ship dates.
• Collaborate with Sales, Graphics, and other teams to ensure graphics projects align with overall commercialization timeline.

TreeHouse Foods is a leading manufacturer of private label packaged foods and beverages, operating a network of over 20 production facilities and several corporate offices across the United States and Canada. Named one of America’s Best Large Employers by Forbes, the company fosters a performance-based culture with a strong set of values and a commitment to excellence.

• Plan and execute marketing projects and programs, supporting regional and local marketing teams.
• Act as super user for key BD tools (Veeva Vault, AdProm, ShowPad) to ensure efficient and compliant marketing processes.
• Support development of marketing materials, website updates, and management of marketing events and congresses.

BD is a global medical technology company that develops and manufactures medical devices and solutions to advance health. With a large, multinational team, BD fosters a culture of collaboration, compliance, and quality.

• Serve as key point of contact between rhode and international distributors and retail partners for supply chain operations.
• Analyze customer supply chain data to improve in-stocks, fulfillment, and service levels.
• Support new market launches and international expansion through cross-functional collaboration.

Rhode is a skincare brand developed by Hailey Rhode Bieber, offering curated essentials for various skin types. Its parent company e.l.f. Beauty has net sales of $1.6B and offers a culture of flexibility, competitive compensation, and half-day Fridays.

• Develop project plans and execute to timelines and budget.
• Serve as primary customer contact ensuring timely communication.
• Ensure compliance with data onboarding protocols and operating procedures.

Beacon Biosignals is developing a leading at-home EEG platform to advance precision medicine for brain disorders. The company values asynchronous remote work and diversity, with a collaborative culture.

• Provide operational leadership and oversight for assigned FSP projects, managing regional trials or supporting complex global trials.
• Serve as the primary operational point of contact for clients, coordinating cross-functional activities and monitoring project risks, resource constraints, and quality trends.
• Contribute to financial oversight, meeting facilitation, and team onboarding, training, and mentoring.

Precision Medicine Group is a clinical research organization (CRO) focused on supporting clients researching ground-breaking cancer therapies. The company fosters a supportive, collaborative environment that promotes work-life balance and team development.

• Serve as primary contact for project-related matters, managing client expectations to ensure satisfaction with PrimeVigilance services.
• Prepare project scope and objectives based on signed agreements, and plan activities including deadlines and interim milestones.
• Report to clients and PrimeVigilance management, including monthly reports for invoicing basis.

PrimeVigilance is a global pharmacovigilance specialist helping clients navigate complex regulations while keeping patient safety at the center of every decision. The company operates across Europe, North America, South America, Asia, and Australia, fostering a culture built on kindness, flexibility, growth, and belonging.

• Creates and maintains project timelines in MS Project or similar systems, ensuring accurate updates and distribution to team members.
• Coordinates internal and external meetings, prepares agendas, takes minutes, and files documentation in the Trial Master File.
• Manages study-specific training, system access, and supplies, while supporting team communications and vendor coordination.

Precision for Medicine is a Clinical Research Organization specializing in precision medicine, combining novel trial designs, operational expertise, and advanced biomarker analytics to advance oncology and rare disease treatments. The company fosters a collaborative, detail-oriented culture with a focus on professional growth and teamwork.

• Monitor and own the progress of clinical studies at investigative sites.
• Ensure studies are conducted per protocol, SOPs, ICH-GCP, and all applicable regulations.
• Coordinate setup activities including investigator identification and regulatory submissions.

Precision for Medicine is a CRO integrating clinical trial execution with scientific and lab expertise, focusing on Oncology and Rare Disease. They have a strong culture with high CRA retention and emphasize work-life balance.

• Lead the strategic development and execution of country-specific growth initiatives.
• Oversee operational performance, regulatory compliance, and market expansion.
• Foster cross-functional collaboration to drive business objectives and customer satisfaction.

Redcare Pharmacy is Europe's No.1 e-pharmacy, powered by passionate teams and cutting-edge innovation. They strive to create a healthy, collaborative work environment where every employee feels valued and inspired to contribute to their vision.

• Manage day-to-day regulatory affairs support, including clinical trial applications and compliance with global regulations.
• Provide expert guidance to project stakeholders, ensuring timely and high-quality service delivery.
• Develop regulatory strategies and tools, staying current with industry best practices and regulatory changes.

Alimentiv provides global regulatory affairs support services for clinical research. The company emphasizes high-quality service delivery, compliance with industry standards, and a collaborative culture.

• Develop, implement, and maintain global trade compliance policies, procedures, controls, and operational processes to support international business activities.
• Ensure compliance with customs regulations, import/export controls, sanctions requirements, and country-specific trade regulations across global markets.
• Lead internal trade compliance reviews, investigations, risk assessments, and corrective action initiatives.

Our partner is a fast-growing, science-driven company focused on innovative global healthcare and precision medicine initiatives. They offer a collaborative international environment with multidisciplinary teams and an inclusive workplace culture emphasizing diversity, integrity, and meaningful impact.

• Provide administrative and operational support for commercial lighting projects from start to finish.
• Coordinate with warehouse, clients, and internal teams to manage orders, freight, and warranty claims.
• Maintain CRM records, prepare quotes, and handle customer inquiries via shared inbox.

An Australian design-led lighting business offering decorative, architectural, and custom lighting solutions. They collaborate with designers and architects, focusing on innovation and sustainable design.

• Support clinical supply planning, label management, and distribution activities for global trials.
• Coordinate with clinical, regulatory, quality, and external partners to ensure timely delivery of materials.
• Assist with IRT system testing, supply strategy setup, and process improvement initiatives.

Jobgether is a recruitment platform that uses AI-powered matching to connect candidates with hiring companies. They focus on streamlining the application process and providing a collaborative work environment.

• Oversee and project manage the Shop and Space Planning team’s workflow, resources, and deadlines for seamless collaboration.
• Maintain process tools, implement sprint projects, and collaborate with cross-functional teams to integrate workflows.
• Conduct regular check-ins, assess team processes, and partner with leadership to identify development opportunities.

Lush Handmade Cosmetics is a cosmetics company known for handmade, ethical products. They are a large multinational with a culture that values purpose, inclusion, and collaboration.

• Provide strategic regulatory input and manage European Clinical Trial Applications (CTA) and amendments.
• Serve as key regulatory liaison for multi-continental oncology projects, collaborating with cross-functional teams.
• Maintain expertise in GCP, EU regulations, and support business development activities.

Theradex Oncology is a full-service CRO specializing in early and late-phase oncology trials globally. Founded in 1982 with over 40 years of experience, the company has managed more than 250 trials and partners with the National Cancer Institute, maintaining a focused culture on cancer drug development.

• Lead project initiation, planning, and execution for API and drug product development projects.
• Serve as liaison between clients, technical teams, and business development to ensure project success.
• Monitor project progress, report to stakeholders, and implement corrective measures using risk assessment tools.

WuXi, through its STA division, provides API and drug product development and manufacturing services. The company is a leading global contract research and manufacturing organization with a focus on small molecule development.

• Lead the study start-up process, developing strategy and coordinating regulatory deliverables to meet targets.
• Serve as primary contact for start-up activities, prepare and review regulatory documents, and ensure compliance with ICH-GCP and regulations.
• Manage essential document collection, site correspondence, contract negotiations, and support team training and budget monitoring.

Ergomed is a mid-sized contract research organization specializing in oncology and rare disease. The company has a global presence with operations in Europe, North America, and Asia, and emphasizes employee well-being, work-life balance, and career development.

• Lead the design and execution of strategic global partner programs, acting as a key link between business strategy and operational delivery.
• Manage a diverse portfolio of initiatives, collaborating with cross-functional stakeholders to improve partner experiences and business outcomes.
• Apply structured project management practices to ensure timelines, milestones, and deliverables are successfully achieved.

Jobgether provides an AI-powered job matching platform to help candidates connect with hiring companies. We focus on ensuring applications are reviewed efficiently and fairly, fostering a global technology environment.

• Manage TMF operations activities for multiple complex studies or sponsor portfolios.
• Oversee Trial Master File quality control including planning, tracking, and reporting.
• Support regulatory inspections and sponsor audits while collaborating with cross-functional teams.

This is a global clinical research environment focused on ensuring accuracy, compliance, and quality of essential trial documentation. The company operates with a collaborative international team and values inclusion, professional growth, and purpose-driven healthcare work.

• Lead strategy and execution of external sterile manufacturing operations, ensuring supplier performance and supply continuity.
• Manage senior-level supplier relationships, governance, and commercial negotiations with third-party manufacturing partners.
• Drive cross-functional alignment across Quality, Supply Chain, and Procurement to optimize network performance.

This position is listed on behalf of a partner company, which manages all applications and next steps. Jobgether is an AI-powered recruitment platform that partners with companies to find top talent.