Clinical Research Scientist – Trials, Data & Publications

Keystone Distinction Group

Lancaster (SC)

On-site

USD 90,000 - 140,000

Full time

14 days+

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Job summary

Keystone Distinction Group seeks a scientist to support clinical development, research ingredient science, and contribute to patent publications. The candidate will collaborate with a cross-functional team, design experiments, and interpret results to drive product advancement.

Requirements include a Masters in life sciences, strong scientific writing, and practical GCP understanding. The role involves coordinating trials, data integrity, and cross-department communication in a fast-paced

Qualifications

Strong candidates translate technical insights into actionable plans.
Experience in a clinical study related role.
Strong scientific writing ability and ability to communicate complex data clearly.
Understanding of GCP Good Clinical Practice guidelines.
Self-motivated, adaptable, and capable in a fast-paced environment.

Responsibilities

Collaborate with the clinical development team in study design and execution.
Manage multiple activities of clinical trials with direction from project leaders.
Prepare and ship trial documentation and correspondence with sites.
Assess protocol compliance with investigators and contract facilities.
Verify study data using data management tools and monitoring processes.
Conduct statistical analyses and generate tables/graphics for study reports.
Prepare scientific publications as needed by the company.
Communicate effectively across departments and teams.