Clinical Scientist

Responsibilities

• Plan and execute clinical trial activities
• Develop data collection, review, and interpretation processes
• Partner with Clinical Safety Scientists and participate in safety review and communication
• Prepare internal (including DMC or steering committee) and external scientific presentations, research manuscripts and review articles, as required
• Partner with Clinical Operations and Data Management to ensure data consistency, quality, integrity, safety, and alignment with company values
• Scientific literature searches and to distill data into concise analysis / reports
• Organize and provide training assistance to departments/vendors (scientific/development improvements)
• Serve as a liaison with internal/external scientific and medical experts to ensure protocol execution is consistent with intent. Coordinate and oversee medical or endpoint-specific training for study protocols
• Assist with planning of, and participate in, Investigator Meetings and Advisory/Scientific boards
• Prepare Data Monitoring Committee (DMC) and/or adjudication charters. Prepare deliverables and participate in periodic review meetings
• Provide scientific expertise to other departments and functions

Preferred

• Masters, PharmD, or PhD preferred
• Glassdoor
• 3.8
• Beacon Hill offers business consulting services.
• Boston, Massachusetts, USA
• https://bhsg.com
• Late Stage
• Leadership Team
• Amy Van Sicklin
• Chief Culture Officer
• Recent News
• Beacon Hill Financial Enters Southern California Market, Strengthening National Reach
• 2025-11-05
• LinkedIn
• Beacon Hill Staffing Group on LinkedIn: #employingthefuture #expertsatwork #gohire
• 2024-04-08
• Beacon Hill Staffing Group on LinkedIn: #employingthefuture #expertsatwork #gohire #staffing100northamerica
• Company data provided by
• AI Tools
• Customize Your Resume

Qualifications

• 2+ years of relevant Clinical Research experience
• Study execution, data review and data management experience
• Experience with domestic and international clinical trials design and study data reporting
• Understanding of the clinical trial stages and key data needs for program progression
• Knowledge of the drug development process including Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) requirements
• Ability to work independently and collaboratively with internal teams, CROs and other key stakeholders, as required, in a fast-paced, multi-disciplinary team environment
• Exemplary critical thinking, planning, organization, and time management skills including the ability to support and prioritize multiple projects
• Solid communication and presentation skills
• Proficient in the use of software relevant to above tasks including Excel
• Masters, PharmD, or PhD preferred

Required skills

• Clinical Practice (GCP), Clinical Research, Clinical Trial Design, Clinical Trial Execution, Data Management, Data Review, Excel, International Conference on Harmonisation (ICH) Requirements, Study Data Reporting

Preferred skills

• 2024-04-08, 2025-11-05, 3.8, AI Tools, Amy Van Sicklin, Analyze How Well You Fit, Beacon Hill offers business consulting services., Boston, Massachusetts, USA, Build Cover Letter, Chief Culture Officer, Company data provided by, Customize Your Resume, Glassdoor, Late Stage, Leadership Team, LinkedIn, Make your application stand out, Masters, PharmD, or PhD preferred, Maximize your interview chances, Recent News, Understand your strength & weakness, https://bhsg.com

Experience

• 2+ years