4 Lead Clinical Research Scientist jobs in whatjobs
Lead Clinical Research Scientist
Posted 14 days ago
Job Viewed
Job Description
Our client is a leading force in medical innovation, and we are seeking a highly accomplished Lead Clinical Research Scientist to drive critical research initiatives. This is a fully remote, full-time position where you will play a pivotal role in the design, execution, and interpretation of clinical trials. You will be responsible for developing comprehensive clinical research protocols, overseeing data collection and analysis, and ensuring compliance with all regulatory guidelines (e.g., FDA, EMA). The ideal candidate will possess a Ph.D. in a relevant life science discipline (e.g., Pharmacology, Biomedical Sciences, Medicine) and have extensive experience in clinical trial management, specifically within the pharmaceutical or biotechnology sectors. Strong expertise in biostatistics, study design, and regulatory affairs is essential. You will lead a team of research associates and collaborate with clinicians, statisticians, and regulatory experts to advance novel therapeutic strategies. This remote role requires exceptional leadership qualities, meticulous attention to detail, and the ability to manage complex projects with precision and independence. Excellent communication and interpersonal skills are vital for effective collaboration across distributed teams and with external partners.
Key Responsibilities:
Key Responsibilities:
- Design and develop robust clinical trial protocols, ensuring scientific rigor and regulatory compliance.
- Oversee the implementation and management of clinical studies, from site initiation to study close-out.
- Lead and mentor a team of clinical research professionals, fostering a high-performance culture.
- Collaborate with biostatisticians to develop statistical analysis plans and interpret study results.
- Ensure adherence to Good Clinical Practice (GCP) guidelines and all applicable regulations.
- Prepare and review study documentation, including investigator brochures, informed consent forms, and clinical study reports.
- Manage relationships with clinical sites, investigators, and external vendors.
- Analyze clinical data, identify trends, and prepare reports for regulatory submissions and publications.
- Stay abreast of scientific advancements, emerging therapeutic areas, and changes in regulatory requirements.
- Contribute to the strategic planning of the research pipeline and the selection of new drug candidates for development.
- Ph.D. in Pharmacology, Biomedical Sciences, Medicine, or a related field.
- Minimum of 8 years of progressive experience in clinical research, drug development, or a related area within the pharmaceutical or biotech industry.
- Demonstrated experience in designing and managing Phase I-IV clinical trials.
- In-depth knowledge of GCP, ICH guidelines, and global regulatory requirements.
- Strong understanding of biostatistics, study design principles, and data management.
- Excellent leadership, project management, and organizational skills.
- Exceptional analytical and problem-solving abilities.
- Outstanding written and verbal communication skills, with the ability to present complex information effectively.
- Proven ability to work independently and collaboratively in a remote setting.
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Lead Clinical Research Scientist
Posted 13 days ago
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Job Description
Our client is seeking a highly accomplished Lead Clinical Research Scientist to spearhead innovative research initiatives in the pharmaceutical sector. This is a fully remote, senior-level position, perfect for a scientist with extensive experience in clinical trial design, execution, and data analysis. You will be responsible for developing clinical research strategies, designing protocols, overseeing the conduct of clinical trials, and ensuring adherence to regulatory standards (e.g., GCP, ICH guidelines). Your role will involve collaborating with cross-functional teams, including R&D, regulatory affairs, and medical affairs, as well as external investigators and academic institutions. You will be instrumental in interpreting complex clinical data, authoring scientific publications and presentations, and contributing to the regulatory submission process. The ideal candidate will possess a Ph.D. or Master's degree in a relevant life science discipline, with a minimum of 7 years of progressive experience in clinical research within the pharmaceutical or biotechnology industry. Proven expertise in designing and managing Phase I-IV clinical trials, strong statistical understanding, and excellent scientific writing skills are essential. Experience in specific therapeutic areas is a plus. This role requires exceptional leadership qualities, the ability to mentor junior scientists, and outstanding communication and interpersonal skills, especially within a remote work environment. If you are passionate about advancing medical science and driving drug development through rigorous clinical research, and you thrive in a flexible, remote setting, we encourage you to apply. This role is associated with our operations in **Nyeri, Nyeri, KE**, but is conducted entirely remotely.
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Lead Clinical Research Scientist
Posted 2 days ago
Job Viewed
Job Description
Our client is seeking a highly qualified and experienced Lead Clinical Research Scientist to spearhead their research initiatives in a fully remote capacity. This role will involve designing, executing, and analyzing clinical studies to advance medical understanding and develop new therapeutic interventions. Though the company's operations are linked to Kisumu, Kisumu, KE , this is a remote-first position, requiring exceptional scientific acumen, project management skills, and the ability to work independently. The ideal candidate will possess a Ph.D. in a relevant scientific field, extensive experience in clinical research, and a strong publication record. You will play a pivotal role in driving cutting-edge research and contributing to significant advancements in healthcare.
Responsibilities:
Responsibilities:
- Lead the design and development of clinical research protocols, ensuring scientific rigor and ethical compliance.
- Oversee the execution of clinical studies, including data collection, monitoring, and management.
- Analyze and interpret complex research data, drawing meaningful conclusions and identifying key findings.
- Prepare comprehensive research reports, manuscripts for publication, and presentations for scientific conferences.
- Collaborate with principal investigators, statisticians, regulatory affairs, and other stakeholders to ensure successful study completion.
- Stay abreast of the latest scientific literature, emerging research methodologies, and technological advancements in the field.
- Contribute to grant writing and funding applications to secure resources for research projects.
- Ensure compliance with all relevant regulatory guidelines (e.g., ICH-GCP) and ethical standards.
- Mentor and guide junior research staff, fostering a collaborative and productive research environment.
- Manage research budgets and resources effectively to ensure project success within defined timelines.
- Evaluate and implement new technologies and methodologies to enhance research capabilities.
- Communicate research findings and strategic direction to internal and external stakeholders.
This advertiser has chosen not to accept applicants from your region.
2
Lead Clinical Research Scientist
Posted 1 day ago
Job Viewed
Job Description
Our client, a prominent pharmaceutical innovator dedicated to advancing global health, is seeking a Lead Clinical Research Scientist to spearhead groundbreaking research initiatives. This is a fully remote position, offering the flexibility to work from anywhere while contributing to the development of life-changing therapies. The successful candidate will play a critical role in the design, execution, and analysis of clinical trials, ensuring adherence to regulatory standards and scientific integrity. Responsibilities include developing clinical trial protocols, managing investigational sites, analyzing and interpreting complex clinical data, and preparing regulatory submissions. You will collaborate closely with cross-functional teams, including regulatory affairs, biostatistics, and medical affairs, to ensure the successful progression of drug development programs. This role requires a deep understanding of pharmaceutical R&D, clinical trial methodologies, and relevant therapeutic areas. The ability to thrive in a remote, fast-paced environment, coupled with strong leadership and communication skills, is essential. You will be responsible for mentoring junior scientists and contributing to strategic decision-making within the clinical development group. The ideal candidate will possess a PhD or MD with substantial postdoctoral experience and a minimum of 5-7 years of experience in clinical drug development within the pharmaceutical or biotechnology industry. Demonstrated success in designing and conducting Phase II-IV clinical trials, with a strong publication record, is highly desirable. Proficiency in data analysis software and a thorough understanding of Good Clinical Practice (GCP) guidelines are required. This opportunity is based in **Thika, Kiambu, KE**, but the role is entirely remote, allowing you to leverage your expertise globally. If you are passionate about scientific rigor and making a tangible impact on patient lives, we encourage you to apply.
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