Senior Scientist

Amgen

. Plan, manage, and monitor in vivo outsourced nonclinical safety studies .

Posted 9/19/2026full-timeRemote • United StatesSenior💰 $129,229 - $174,839 per yearWebsite

Core Competencies

Role fit

Core Competencies

Use this summary to align your resume positioning with the role.

Demonstrates expertise in managing in vivo nonclinical safety studies, including study protocol oversight, data analysis, and effective communication with study teams. Proficient in GLP guidelines and experienced in collaborating with Contract Research Organizations.

Highest-signal resume keywords

In Vivo Nonclinical Safety ManagementGLP Guidelines ExperienceStudy Director ExperienceData Analysis and CommunicationPeople Management Experience

ATS Keywords

Tailor your resume

Applicant Tracking System Keywords

Tip: use these terms in your resume and cover letter to boost ATS matches.

Hard Skills

Nonclinical Safety StudiesData InterpretationStudy Management PrinciplesScientific WritingSOP Development

Soft Skills

Strong Communication SkillsNegotiation SkillsTeam CollaborationAdaptabilityLeadership

Tools & Technologies

Graphing SoftwareMicrosoft OfficePlaniswareGantt Charts

Industry Keywords

Contract Research OrganizationsStudy MonitoringPerformance ManagementScientific PresentationsDepartmental Initiatives

About the role

Key responsibilities & impact

Plan, manage, and monitor in vivo outsourced nonclinical safety studies
Serve as the primary contact for study protocols, study activities, and reports, working directly with Study Directors and study teams
Travel up to 30% for onsite study monitoring and team meetings
Prepare scientific figures and presentations
Organize and interpret data
Adapt scientific and technical information for broader audiences
Write departmental guidelines and SOPs
Participate in departmental initiatives
Facilitate meetings and report study status
Manage complex issues and coordinate resolution plans involving multiple parties

Requirements

What you’ll need

Master’s degree with 4 or more years of relevant experience in nonclinical safety, or Bachelor’s degree with 6 or more years of relevant experience in nonclinical safety
Ability to review, analyze, and communicate in vivo nonclinical safety data and results
Experience with GLP guidelines
Experience as a study director, study monitor, or study coordinator in nonclinical safety in vivo studies
Experience applying program and study management principles and skills in a scientific setting
Experience working and collaborating with Contract Research Organizations
Ability to interpret and deliver results in a team environment
Strong negotiation and influencing skills
Ability to adjust to a dynamic and collaborative work environment
Ability to lead and embrace change
Strong communication skills
Previous people-management experience, including coaching, performance management, and staff development
Proficiency with graphing software, Microsoft Office, Planisware or similar timeline management software, and Gantt charts
Sponsorship for this role is not guaranteed

Benefits

Comp & perks

Retirement and Savings Plan with generous company contributions
Group medical, dental and vision coverage
Life and disability insurance
Flexible spending accounts
Discretionary annual bonus program
Stock-based long-term incentives
Award-winning time-off plans
Flexible work models where possible
Career development opportunities
Work/life balance support