Senior Scientist, Clinical Research

About this role

Job Description

The Early Clinical Scientist (ECS) coordinates the design, planning and execution of early phase clinical trials with the Clinical Director, and internal/external team members.  Oversees trials within and/or across program(s)/therapeutic areas and ensures excellence in execution/compliance to support study objectives and data validity. Manages internal/external team performance to achieve project objectives and resolves project performance issues if they arise.   

Ensures appropriate clinical safety assessment and risk management of compounds. Conducts real-time oversight of ongoing trials to identify and mitigate patient, study design, data or study conduct issues.  Reviews and interprets clinical trial data. May conduct on-site study monitoring, including site training & supervision of complex, novel endpoint/biomarker collection processes.  Applies thorough knowledge of GCP, ICH guidelines and regulatory requirements for clinical development.   

Represents Early Stage Development on cross-functional teams to develop and/or improve internal job aids/SOP/clinical development procedures.  Identifies and communicates best practices within the organization.  Promotes departmental adaptation of new procedures.   

Technical Writing & Communications   Co-authors clinical sections of protocols, clinical investigator brochures, clinical study reports, Worldwide Marketing Application/Common Technical Document (WMA/CTD) subsections, and regulatory agency update and safety reports, as well as clinical development plans, publications, and abstracts. Ensures documents are completed in accordance with applicable standards.  Develops study operational documents with input from team members (e.g. site monitoring plan, study operations manual, informed consent, etc.).  

Project Management   Manages trial and program projects including team activities (i.e. meetings, document/collaborative workspace management, etc.), provides risk assessment and contingency planning, under accelerated timelines.  Familiar with early drug development processes, building knowledge and skills to effectively manage additional processes/procedures.   

Education Minimum Requirement:   • Degree in Life Sciences 

• Bachelor’s degree and ≥6 years related* experience, OR 

• Master’s degree and ≥4 years related* experience, OR 

• PhD or doctorate with ≥2 years related* experience 

*e.g., knowledge of clinical trial management and trial execution; clinical site training/monitoring; medical and regulatory writing

Required Experience and Skills:    • At least 3 years experience in an operational clinical scientist or study manager role in clinical research at a pharmaceutical or biotech company.

• Understanding of clinical research development process from program planning to regulatory submission

• Able to quickly develop a working scientific knowledge of different therapeutic areas 

• Ability to manage complex operations and projects under accelerated timelines 

• Scientific, medical and/or safety writing and reporting (at least one is required)

• Ability to partner effectively with internal and external teams to achieve results 

• Strong team collaboration, leadership, communication (written & verbal), issue identification and resolution skills 

• Knowledge of GCP, ICH guidelines and regulatory requirements 

Preferred Experience and Skills:   • Global Phase I subject and patient trials, safety reporting, and regulatory WMA submission experience a plus.

• Experience managing Immunology and/or vaccine trials with an ability to think outside of the box, explore novel ways of working and comfortably navigate ambiguity to drive results also a plus.

Required Skills: Adaptability, Adaptability, Biopharmaceutical Industry, Clinical Development, Clinical Research, Clinical Study Management, Clinical Trial Planning, Clinical Trials, Clinical Trials Analysis, Drug Development, Ethical Compliance, Ethical Standards, ICH GCP Guidelines, Immunology, Medical Writing, Multiple Therapeutic Areas, Phase I Studies, Project Management, Protocol Development, Regulatory Requirements, Regulatory Submissions, Regulatory Writing, Risk Assessments, Scientific Publications, Technical Writing {+ 1 more} Preferred Skills:

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Current Contingent Workers apply HERE

US and Puerto Rico Residents Only:

Our company is committed to inclusion, ensuring that candidates can engage in a hiring process that exhibits their true capabilities. Please click here if you need an accommodation during the application or hiring process. As an Equal Employment Opportunity Employer, we provide equal opportunities to all employees and applicants for employment and prohibit discrimination on the basis of race, color, age, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability status, or other applicable legally protected characteristics.  As a federal contractor, we comply with all affirmative action requirements for protected veterans and individuals with disabilities.  For more information about personal rights under the U.S. Equal Opportunity Employment laws, visit:

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We are proud to be a company that embraces the value of bringing together, talented, and committed people with diverse experiences, perspectives, skills and backgrounds. The fastest way to breakthrough innovation is when people with diverse ideas, broad experiences, backgrounds, and skills come together in an inclusive environment. We encourage our colleagues to respectfully challenge one another’s thinking and approach problems collectively.

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The salary range for this role is $117,000.00 - $184,200.00 This is the lowest to highest salary we in good faith believe we would pay for this role at the time of this posting. An employee’s position within the salary range will

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