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Clinical Research Scientist
Actalent • Remote • Posted 2 days ago
Clinical Research Scientist
Actalent • Remote • Posted 2 days ago
Remote • Full-time • $90.00-$95.00/hr • Senior Level
We have an immediate opening for a Clinical Research Scientist ( Fully Remote Position )
What you will need to be considered:
+ 5+ years of data review experience.
+ 3+ years of data review in oncology, particularly with solid tumors and phase 1 clinical trials.
+ Completion of a PhD Or MD in a relevant field.
+ Proficient in study design, con med, and lab review.
+ Proficient knowledge and skills to support program-specific data review, trend identification, and data interpretation.
+ Strong medical terminology and medical writing skills.
+ Knowledge of ICH, GCP, and other relevant regulatory guidelines.
+ Ability to analyze clinical information succinctly and efficiently.
+ Strong written communication skills for developing clinical protocols and presenting trial results.
+ Outstanding communication, presentation, analytic, and strategic capabilities.
+ Ability to collaborate with medical experts and all levels of management in a cross-functional team environment.
Job Responsibilities:
+ Develop and review study protocols with minimal guidance, ensuring a high-quality final document.
+ Prepare and present reports and presentations on clinical research findings.
+ Regularly review information to check safety procedures, efficiency, and lab data accuracy.
+ Review and validate clinical study reports (CSRs) with a thorough understanding of the data.
+ Contribute to, coordinate, and review regulatory documents, Consent Forms (ICF), and other study materials.
+ Collaborate with Clinical/Medical Affairs, Clinical Operations, Drug Safety, Regulatory Affairs, and external vendors.
+ Meet deadlines and milestones based on assigned study goals.
+ Participate in protocol design, writing, and implementation to meet GCP, ICH, and regulatory requirements.
+ Provide input into the drug development and evidence generation process as a technical expert.
+ Perform data review tasks, comprising 80% of the role.
Additional Skills & Qualifications
+ Experience in oncology and solid tumors is required.
+ Phase 1 / Early Phase Experience.
Pay and Benefits
The pay range for this position is $90.00 - $95.00/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 Mar 27, 2025.
About Actalent
Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
Diversity, Equity & Inclusion
At Actalent, diversity and inclusion are a bridge towards the equity and success of our people. DE&I are 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
The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email actalentaccommodation@actalentservices.com (%20actalentaccommodation@actalentservices.com) for other accommodation options.
What you will need to be considered:
+ 5+ years of data review experience.
+ 3+ years of data review in oncology, particularly with solid tumors and phase 1 clinical trials.
+ Completion of a PhD Or MD in a relevant field.
+ Proficient in study design, con med, and lab review.
+ Proficient knowledge and skills to support program-specific data review, trend identification, and data interpretation.
+ Strong medical terminology and medical writing skills.
+ Knowledge of ICH, GCP, and other relevant regulatory guidelines.
+ Ability to analyze clinical information succinctly and efficiently.
+ Strong written communication skills for developing clinical protocols and presenting trial results.
+ Outstanding communication, presentation, analytic, and strategic capabilities.
+ Ability to collaborate with medical experts and all levels of management in a cross-functional team environment.
Job Responsibilities:
+ Develop and review study protocols with minimal guidance, ensuring a high-quality final document.
+ Prepare and present reports and presentations on clinical research findings.
+ Regularly review information to check safety procedures, efficiency, and lab data accuracy.
+ Review and validate clinical study reports (CSRs) with a thorough understanding of the data.
+ Contribute to, coordinate, and review regulatory documents, Consent Forms (ICF), and other study materials.
+ Collaborate with Clinical/Medical Affairs, Clinical Operations, Drug Safety, Regulatory Affairs, and external vendors.
+ Meet deadlines and milestones based on assigned study goals.
+ Participate in protocol design, writing, and implementation to meet GCP, ICH, and regulatory requirements.
+ Provide input into the drug development and evidence generation process as a technical expert.
+ Perform data review tasks, comprising 80% of the role.
Additional Skills & Qualifications
+ Experience in oncology and solid tumors is required.
+ Phase 1 / Early Phase Experience.
Pay and Benefits
The pay range for this position is $90.00 - $95.00/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 Mar 27, 2025.
About Actalent
Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
Diversity, Equity & Inclusion
At Actalent, diversity and inclusion are a bridge towards the equity and success of our people. DE&I are 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
The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email actalentaccommodation@actalentservices.com (%20actalentaccommodation@actalentservices.com) for other accommodation options.