Job Information
Actalent Senior Clinical Scientist in Raleigh, North Carolina
Job Title: Senior Clinical ScientistJob Description
The Senior Clinical Scientist serves as a key member of the Aesthetics Research and Development team and contributes scientific and strategic expertise to global clinical programs. This role partners closely with cross-functional study teams to shape clinical strategy, study design, and execution, as well as data analysis and interpretation, with the goal of supporting the registration of new aesthetic products and novel indications. The position starts as a six‑month fixed‑term contract, with the potential to transition to a permanent role based on business needs and individual performance.
Responsibilities
Provide scientific and strategic input across all stages of clinical development to support market approval for new aesthetic products and novel indications.
Contribute to the design of clinical trials for medical devices, drugs, biologics, and other products for human use, spanning in‑development through post‑marketing studies.
Work as an integral member of cross‑functional teams of internal and external experts, supporting the clinical director in developing and executing clinical strategies.
Coordinate and integrate data and information from internal and external studies, research documentation, and published literature to support clinical development initiatives.
Consolidate input from internal and external contributors to develop clear and appropriate key clinical and scientific messages.
Support early‑phase development activities by curating, reviewing, and interpreting preclinical and exploratory data.
Provide scientific guidance and technical expertise within teams and across departments, offering strategic, actionable direction and constructive feedback to build strong team unity and identity.
Identify and troubleshoot study‑specific issues, competing priorities, and clinical or scientific challenges, and help drive resolution.
Ensure effective, accurate, and timely communication of key issues, risks, and progress to project teams and Senior leadership.
Support the planning and preparation of internal and external stakeholder meetings, including workshops, summits, investigator meetings, scientific advisory boards, and regulatory meetings.
Write, review, edit, and approve high‑quality clinical documents such as clinical study outlines, clinical investigation plans and amendments, clinical investigation reports, and investigators’ brochures, where applicable.
Interpret and synthesize data from clinical studies, including tables, figures, listings, and peer‑reviewed literature, and provide meaningful scientific interpretation and feedback to stakeholders.
Collaborate effectively with multidisciplinary, international teams to execute project plans and deliverables.
Ensure all clinical documents comply with local and international regulations, laws, scientific and regulatory guidance, Good Clinical Practice (GCP), and internal policies and procedures.
Proactively identify risks in clinical programs and documentation, escalate current and potential issues, and propose and implement solutions, including contingency plans.
Ensure successful execution, review, and presentation of critical clinical documents to leadership and other key stakeholders.
Contribute scientific expertise to trial set‑up and execution, including the interpretation and reporting of study results.
Support the selection of relevant clinical outcome assessments (COAs) as part of a cross‑functional team.
Provide scientific input into the development and validation of project‑specific COAs.
Provide scientific input for the clinical components of regulatory and project documents, including Clinical Evaluation Plans (CEP) and Reports (CER), Instructions for Use, and Post‑Market Clinical Follow‑up Plans (PMCFP) and Reports (PMCFR).
Contribute to the appropriate disclosure of clinical trial data in public registries, ensuring clarity, accuracy, and regulatory compliance.
Prepare, review, and present clinical trial data to internal and external stakeholders using clear, concise, and consistent result summaries.
Provide scientific and written expertise for manuscripts, abstracts, and poster submissions in collaboration with R&D, Medical Affairs, and Commercial colleagues.
Apply knowledge of Good Publication Practices and editorial policies to ensure high‑quality, compliant publication outputs.
Effectively manage assigned medical writing projects, including those outsourced to external vendors.
Oversee and review the work of external medical writing vendors to ensure adherence to standard operating procedures, correct use of templates, and maintenance of high quality standards.
Essential Skills
Demonstrated experience in clinical development and clinical trials, including understanding of end‑to‑end clinical product development.
Experience supporting or contributing to global regulatory submissions in a clinical or scientific capacity.
Strong knowledge of FDA and/or EMA regulations, Good Clinical Practice (GCP), ICH guidelines, and relevant ISO standards.
Excellent verbal and written English skills, including mastery of clinical and technical terminology and standardized scientific writing styles.
Proven ability to interpret, analyze, and synthesize clinical study data, preclinical data, and peer‑reviewed literature.
Ability to work on multiple projects simultaneously while effectively managing competing priorities, timelines, and quality standards.
High adaptability and comfort with changing priorities and evolving project needs.
Strong time management skills to plan, prioritize, and deliver complex documentation and project tasks on schedule.
Advanced problem‑solving skills to identify issues, evaluate options, and implement effective solutions in clinical and regulatory contexts.
Strong communication skills to convey complex scientific concepts clearly to diverse stakeholders.
Demonstrated leadership capabilities, including the ability to provide direction, feedback, and motivation within cross‑functional teams.
Effective collaboration skills to work productively with multidisciplinary, international teams and external partners.
Project management skills to plan, coordinate, and track clinical documentation and related activities.
Ability to motivate and influence others to align with clinical strategy and project objectives.
Emotional intelligence and resiliency to navigate a dynamic, fast‑paced environment while maintaining constructive relationships.
Digital acumen to work efficiently with modern digital tools and platforms used in clinical research and documentation.
Minimum qualification of a Master’s degree in Life Sciences or a closely related discipline.
Additional Skills & Qualifications
Preferred advanced degree such as a PhD or MD in a relevant scientific or medical field.
Experience in aesthetics, dermatology, or related therapeutic areas is beneficial.
Experience working with medical devices, drugs, biologics, or other products for human use across development and post‑marketing phases.
Familiarity with Good Publication Practices and editorial policies for scientific and medical publications.
Experience overseeing external medical writing vendors, including quality review and process adherence.
Ability to build strong, cohesive teams and foster a sense of shared purpose and identity.
Strong interpersonal skills to collaborate effectively with R&D, Medical Affairs, Commercial, and other cross‑functional partners.
Work Environment
This role operates in a 100% remote work environment during the initial consulting period, with standard hours of Monday through Friday, 8:00 a.m. to 4:00 p.m. Eastern Time. Work is highly collaborative and involves regular interaction with multidisciplinary and international teams using digital communication and project management tools. The position focuses on aesthetics clinical research, supporting an award‑winning portfolio of injectables, devices, and skincare products designed to enhance confidence and quality of life. The organization offers a people‑focused culture that values work–life balance and encourages individuals to live their best lives while pursuing a meaningful career in aesthetic medicine. If the consultant transitions into a permanent role, relocation to Raleigh, North Carolina, is expected within three months, in line with applicable policies and mutual agreement.
Job Type & Location
This is a Contract position based out of Raleigh, NC.
Pay and Benefits
The pay range for this position is $85.00 - $90.00/hr.
Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following: • Medical, dental & vision • Critical Illness, Accident, and Hospital • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available • Life Insurance (Voluntary Life & AD&D for the employee and dependents) • Short and long-term disability • Health Spending Account (HSA) • Transportation benefits • Employee Assistance Program • Time Off/Leave (PTO, Vacation or Sick Leave)
Workplace Type
This is a fully remote position.
Application Deadline
This position is anticipated to close on Apr 22, 2026.
Diversity, Equity & Inclusion
At Actalent, diversity and inclusion are a bridge towards the equity and success of our people. DE&I is embedded into our culture through:
Hiring diverse talent
Maintaining an inclusive environment through persistent self-reflection
Building a culture of care, engagement, and recognition with clear outcomes
Ensuring growth opportunities for our people
Actalent is an equal opportunity employer.
About Actalent
Actalent is a global leader in engineering and sciences services. For more than 40 years, we’ve helped visionary companies advance their goals. Headquartered in the United States, our teams span 150 offices across North America, EMEA, and APAC—with four delivery centers in India led by 1,000+ extraordinary employees who connect their passion with purpose every day.
Our Bangalore, Hyderabad, Pune, and Chennai delivery centers are hubs of engineering expertise, with core capabilities in mechanical and electrical engineering, systems and software, and manufacturing engineering. Our teams deliver work across multiple industries including transportation, consumer and industrial products, and life sciences. We serve more than 4,500 clients, including many Fortune 500 brands. Learn more about how we can work together at actalentservices.com.