Randstad Life Sciences US

About the Company

Randstad North America, Inc. is a wholly-owned subsidiary of Randstad N.V., the world's largest HR services provider. Driven to become the world's most valued 'working life partner', supporting as many people as possible in realizing their true potential throughout their working life, we provide companies with the high quality, diverse, and agile workforces they need while helping people get rewarding jobs and stay relevant in the ever-changing world of work. In 2021, Randstad had on average 39,530 corporate employees and generated revenue of EUR 24.6 billion. Randstad's North American operations comprise 5,700+ associates and a deployed workforce of more than 86,000 in the U.S. and Canada. In addition to staffing and recruitment, Randstad offers outsourcing, consulting and workforce management solutions for generalist and specialist disciplines, including technology, engineering, accounting and finance, clinical and non-clinical healthcare, human resources, legal, life sciences, manufacturing and logistics, office and administration and sales and marketing. Global concepts available to North American client companies include RPO, MSP, integrated talent solutions, payrolling and independent contractor management and career transition services. Learn more at www.randstadusa.com or www.randstad.ca.

Listed Jobs

Company Name

Randstad Life Sciences US

Job Title

Director, Global Launch Excellence Lead)

Job Description

Cambridge, United states

Hybrid

Senior

26-09-2025

Company Name

Randstad Life Sciences US

Job Title

Clinical Scientist

Job Description

**Job Title:** Clinical Scientist **Role Summary:** Provide scientific and clinical expertise to design, execute, and interpret clinical trials within a clinical development program, ensuring high‑quality data that supports product strategy. **Expectations:** - 3–5 years of clinical research experience. - Ability to work independently with limited supervision. - Strong cross‑functional collaboration. **Key Responsibilities:** - Review, interpret, and communicate efficacy and safety data. - Develop clinical development strategy, including plans, product profiles, and draft labels. - Draft and review study protocols, investigator brochures, clinical study reports, informed consent documents, and regulatory submissions. - Design and maintain electronic databases (IRT) and oversee data quality and completeness. - Contribute to scientific education of internal and external stakeholders; engage opinion leaders. - Ensure compliance with Good Clinical Practice, pharmacovigilance, SOPs, and other quality standards. **Required Skills:** - Clinical trial methodology and protocol design. - Clinical Development Strategy. - Clinical Study Report (CSR) preparation. - Interactive Response Technology (IRT) systems. - Regulatory and compliance knowledge. **Required Education & Certifications:** - Bachelor’s degree in a scientific discipline (MS, PhD, PharmD preferred). - No specific certifications required; familiarity with GCP and related regulations preferred.

Waltham, United states

On site

01-10-2025