Senior Consultant - Health Scientist
Listed on 2026-05-16
-
Research/Development
Research Scientist, Clinical Research -
Healthcare
Clinical Research
Job Description
Boston or Westford or Amherst in Massachusetts or Portland, Maine, United States. Applicants must be currently authorized to work in the United States on a full‑time basis. No sponsorship is available.
We prefer the position be located in Amherst or Westford, Massachusetts, and we will consider Boston, Massachusetts, or Portland, Maine. Ramboll has adopted a hybrid model of work, allowing a combination of remote and in‑office engagement.
We invite you to bring your health sciences background into play as you assist our clients in protecting and promoting the health and safety of their employees, customers, and communities through identifying and managing the risks associated with chemical and biological exposures. To succeed in this role, you must have a graduate degree in epidemiology, toxicology, public health, or a related discipline with 3–5 years of experience.
Demonstrated capability to critically evaluate and synthesize scientific literature is essential. Knowledge of the principles of risk assessment will be helpful. Knowledge of one or more Federal regulatory programs and agency requirements and practices (EPA, FDA) is a bonus. Project management experience in a consulting setting will give you an edge.
- Conducting critical reviews of the epidemiological and/or toxicological literature and drafting reports summarizing and synthesizing the results with attention to sources of bias and their potential effects on study results.
- Identifying gaps and research needs in the current evidence base for selected topics.
- Accepting responsibility for the quality and timeliness of reports, and for adherence to budgetary and other project proposal features.
- Participating in the preparation of proposals, including providing input on work plans and schedules.
- Master's degree in epidemiology, toxicology, or a related field.
- 3 to 5 years of professional experience analyzing and interpreting scientific publications, including conducting systematic, critical reviews of the literature.
- Excellent oral and written communication skills.
- Strong work ethic and great time management practices that enable you to prioritize multiple, competing project deadlines.
- Attention to detail, combined with understanding of the broader context and purpose.
- Comfort working both independently and as part of a team.
- Self‑directed initiative to improve and advance technical capabilities and skills.
- Proficiency with MS Office and relevant analytical programs.
All your information will be kept confidential according to EEO guidelines.
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