677 Senior Clinical Research Associate Pharmaceuticals Remote jobs in Kenya
Senior Clinical Research Associate - Pharmaceuticals (Remote)
Posted 21 days ago
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Job Description
Our client is a leading pharmaceutical company dedicated to advancing global health, seeking a highly experienced Senior Clinical Research Associate (CRA) to join their remote clinical operations team. This position is 100% remote, offering flexibility and the opportunity to contribute to critical drug development programs from your home. You will be responsible for monitoring clinical trials, ensuring data integrity, adherence to protocols, and compliance with regulatory requirements. Your role is crucial in bringing life-changing therapies to market.
Responsibilities:
Qualifications:
Responsibilities:
- Conduct remote site monitoring visits and assessments to ensure protocol adherence and data accuracy.
- Manage and mentor clinical trial sites, providing guidance and support to investigators and site staff.
- Verify the accuracy, completeness, and consistency of clinical trial data.
- Ensure compliance with Good Clinical Practice (GCP) guidelines, regulatory requirements, and study protocols.
- Identify, evaluate, and select potential clinical trial sites.
- Prepare monitoring reports and escalate any site issues or concerns promptly.
- Train site personnel on study procedures, data collection, and regulatory requirements.
- Manage drug accountability and investigational product supply at sites.
- Contribute to the development and review of clinical trial documents.
- Collaborate effectively with internal project teams, including project managers, data managers, and biostatisticians.
Qualifications:
- Bachelor's degree in Life Sciences, Nursing, Pharmacy, or a related field.
- Minimum of 5 years of experience as a Clinical Research Associate, with significant experience in remote monitoring.
- In-depth knowledge of ICH-GCP guidelines and regulatory requirements for clinical trials.
- Proven ability to conduct thorough site monitoring and data review.
- Strong understanding of pharmaceutical drug development process.
- Excellent communication, interpersonal, and organizational skills.
- Ability to work independently and manage time effectively in a remote environment.
- Proficiency in clinical trial management systems (CTMS) and electronic data capture (EDC) systems.
- Willingness to travel occasionally as required (though the role is primarily remote).
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Clinical Research Associate (Pharmaceutical) - Remote
Posted 14 days ago
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Job Description
Our client, a leading pharmaceutical organization, is seeking a qualified and diligent Clinical Research Associate (CRA) to join their expanding team. This role is entirely remote, focusing on the monitoring and management of clinical trials to ensure adherence to protocols, good clinical practice (GCP), and regulatory requirements. You will play a crucial role in the drug development process, contributing to the successful execution of studies that bring innovative treatments to patients. The ideal candidate will possess a strong background in clinical research, excellent organizational skills, and the ability to work independently with meticulous attention to detail. A thorough understanding of regulatory landscapes and study procedures is essential.
Key Responsibilities:
This is a fully remote position requiring significant travel (typically 50-75%) to clinical sites as needed, managed effectively within the remote work structure. You must possess strong communication, interpersonal, and problem-solving skills, with the ability to build rapport and trust with site personnel. Excellent time management and organizational abilities are crucial for managing multiple sites and responsibilities effectively. Proficiency with clinical trial management systems (CTMS) and electronic data capture (EDC) systems is highly desirable. The flexibility of this role allows for dedicated focus on site management while coordinating seamlessly with the broader project team, contributing to the critical advancement of pharmaceutical research and development. We are looking for a dedicated professional committed to ensuring the integrity and quality of clinical trials.
Key Responsibilities:
- Perform site selection, initiation, monitoring, and close-out visits for clinical trial sites.
- Ensure compliance with study protocols, investigator brochures, and standard operating procedures (SOPs).
- Verify the accuracy, completeness, and timeliness of clinical data by reviewing source documents and case report forms (CRFs).
- Monitor patient safety and report adverse events as per regulatory guidelines.
- Train and support investigators and site staff on study-related procedures.
- Manage communication between study sites, sponsors, and regulatory authorities.
- Ensure that investigational products are managed, stored, and dispensed correctly.
- Prepare monitoring reports and discuss findings with site personnel and study management.
- Maintain accurate and up-to-date study documentation and regulatory files.
- Participate in team meetings and contribute to the overall success of the clinical development program.
This is a fully remote position requiring significant travel (typically 50-75%) to clinical sites as needed, managed effectively within the remote work structure. You must possess strong communication, interpersonal, and problem-solving skills, with the ability to build rapport and trust with site personnel. Excellent time management and organizational abilities are crucial for managing multiple sites and responsibilities effectively. Proficiency with clinical trial management systems (CTMS) and electronic data capture (EDC) systems is highly desirable. The flexibility of this role allows for dedicated focus on site management while coordinating seamlessly with the broader project team, contributing to the critical advancement of pharmaceutical research and development. We are looking for a dedicated professional committed to ensuring the integrity and quality of clinical trials.
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Remote Pharmaceutical Formulation Scientist - Drug Development
Posted 15 days ago
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Job Description
Our client, a rapidly growing pharmaceutical company dedicated to developing life-changing therapies, is seeking a highly skilled and innovative Remote Pharmaceutical Formulation Scientist. This is a fully remote position, enabling you to contribute to groundbreaking drug development from anywhere. You will be responsible for designing, developing, and optimizing novel drug delivery systems and formulations for both small molecules and biologics. Your expertise will be critical in translating preclinical research into viable, manufacturable drug products. This role involves extensive laboratory work (potentially through collaboration with external labs or supported home labs), data analysis, and scientific documentation. You will collaborate closely with chemists, pharmacologists, and manufacturing teams to advance drug candidates through the development pipeline. A strong understanding of pharmaceutics, physical chemistry, and regulatory requirements is essential.
Responsibilities:
Responsibilities:
- Design and develop stable, effective, and manufacturable pharmaceutical formulations for various routes of administration.
- Investigate and characterize drug substances and excipients to understand their impact on formulation performance.
- Conduct formulation development studies, including pre-formulation, formulation screening, optimization, and stability testing.
- Utilize various drug delivery technologies and approaches to enhance bioavailability, targeted delivery, or patient compliance.
- Perform analytical testing to characterize formulations, such as dissolution, particle size analysis, and viscosity.
- Scale-up formulation processes from laboratory bench to pilot scale.
- Prepare comprehensive technical reports, research summaries, and regulatory submission documents.
- Collaborate with analytical development, process development, and regulatory affairs teams.
- Stay current with scientific literature, emerging technologies, and regulatory guidelines in pharmaceutics and drug delivery.
- Troubleshoot formulation-related challenges and provide scientific insights.
- Ph.D. or Master's degree in Pharmaceutical Sciences, Pharmaceutics, Chemical Engineering, Chemistry, or a related discipline.
- Minimum of 5 years of experience in pharmaceutical formulation development within the industry.
- Proven track record of successful formulation development for small molecules and/or biologics.
- Hands-on experience with various dosage forms (e.g., oral solids, injectables, topical).
- Proficiency in analytical techniques relevant to formulation characterization.
- Strong understanding of physical chemistry, materials science, and biopharmaceutics.
- Familiarity with Good Manufacturing Practices (GMP) and regulatory submission requirements (e.g., FDA, EMA).
- Excellent problem-solving, critical thinking, and data analysis skills.
- Strong written and verbal communication skills, with the ability to present complex scientific information clearly.
- Demonstrated ability to work independently and manage research projects effectively in a remote setting.
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Senior Clinical Research Associate - Remote (Pharmaceutical)
Posted 2 days ago
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Job Description
Our client, a rapidly expanding pharmaceutical company focused on innovative drug development, is seeking a highly experienced Senior Clinical Research Associate (CRA) to join our fully remote global clinical operations team. This critical role will oversee and manage clinical trial sites, ensuring adherence to study protocols, regulatory requirements, and Good Clinical Practice (GCP) guidelines. The ideal candidate will have a comprehensive understanding of the drug development lifecycle, extensive experience in clinical monitoring, and a proven ability to manage multiple complex clinical trials. Your responsibilities will include conducting site qualification, initiation, interim monitoring, and close-out visits (remotely or in-person as required, but the role itself is remote-based). You will be responsible for verifying the accuracy and completeness of clinical data, ensuring patient safety, and managing site personnel to achieve trial objectives. Strong communication and interpersonal skills are essential for building and maintaining effective relationships with investigators, site staff, and internal project teams. This position requires a meticulous attention to detail, exceptional organizational skills, and the ability to proactively identify and resolve issues. Experience with electronic data capture (EDC) systems and clinical trial management systems (CTMS) is mandatory. As this is a fully remote role, you must possess strong self-management capabilities, excellent virtual collaboration skills, and the ability to work independently with minimal supervision. Travel may be required for essential site visits, but the base role is remote. Contributions to study documentation, including protocols, informed consent forms, and study reports, will also be part of your remit. A background in life sciences, nursing, or a related healthcare field, coupled with significant CRA experience, is essential. This is an exceptional opportunity to contribute to life-changing pharmaceutical research from anywhere, supporting global clinical operations that impact patient care worldwide, including potentially near **Nairobi, Nairobi, KE**. Our client offers a competitive salary, comprehensive benefits, and opportunities for professional growth within a cutting-edge pharmaceutical environment.
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Senior Clinical Research Associate - Pharmaceutical (Remote)
Posted 7 days ago
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Job Description
Our client, a leading Pharmaceutical company dedicated to improving global health outcomes, is seeking an experienced Senior Clinical Research Associate (CRA) to join their fully remote team. This pivotal role will involve managing and overseeing clinical trial sites to ensure data integrity, patient safety, and adherence to study protocols and regulatory requirements. You will be responsible for site selection, initiation, monitoring, and close-out activities. This includes conducting routine monitoring visits, verifying source data against case report forms (CRFs), ensuring compliance with Good Clinical Practice (GCP) guidelines, and resolving any site-related issues promptly. You will serve as the primary point of contact for investigators and site staff, fostering strong, collaborative relationships. The ideal candidate will possess a Bachelor's degree in a life science, nursing, or related field, with a minimum of 5 years of progressive experience as a CRA in the pharmaceutical industry. A comprehensive understanding of clinical trial processes, ICH guidelines, and regulatory requirements is essential. Excellent communication, interpersonal, and organizational skills are crucial for effectively managing multiple study sites and diverse teams. The ability to work autonomously, manage your time efficiently, and travel as needed (though primarily remote) is required. Experience with electronic data capture (EDC) systems and various clinical trial management systems (CTMS) is expected. This role offers a unique opportunity to contribute to life-changing drug development programs from a remote setting, ensuring the highest standards of clinical research are maintained, impacting patients worldwide, with an operational base near Mlolongo, Machakos, KE .
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Senior Pharmaceutical Formulation Scientist - Drug Development
Posted 7 days ago
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Job Description
Our client, a progressive pharmaceutical company, is looking for a Senior Pharmaceutical Formulation Scientist to join our dynamic drug development team. This is a fully remote position, allowing you to contribute to groundbreaking pharmaceutical research from your home office. The successful candidate will be responsible for the design, development, and optimization of novel drug formulations for a wide range of therapeutic areas. You will conduct pre-formulation studies, select appropriate excipients, and develop robust manufacturing processes for both solid and liquid dosage forms. Key responsibilities include performing stability studies, characterizing formulations using various analytical techniques, and preparing documentation for regulatory submissions. You will collaborate closely with analytical development, quality control, and regulatory affairs departments to ensure successful product development. This role requires a deep understanding of pharmaceutical sciences, drug delivery systems, and regulatory guidelines. The ideal candidate holds a Master's or Ph.D. in Pharmaceutical Sciences, Chemistry, Chemical Engineering, or a related discipline, with at least 5 years of hands-on experience in pharmaceutical formulation development. Proven expertise in developing various dosage forms, including oral solid, parenteral, and topical formulations, is essential. Experience with controlled-release technologies and bioavailability enhancement is highly desirable. Strong analytical, problem-solving, and project management skills are critical. Excellent written and verbal communication abilities are necessary for effective collaboration and documentation in this remote setting. This opportunity offers the chance to significantly contribute to the pipeline of innovative medicines and advance your career in pharmaceutical research and development, working remotely with a collaborative and forward-thinking team. You will be at the forefront of creating new therapeutic solutions that can improve patient outcomes globally. The position demands a meticulous approach to scientific investigation and a commitment to delivering high-quality, effective pharmaceutical products.
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Principal Pharmaceutical Scientist - Drug Discovery and Development
Posted 17 days ago
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Job Description
Our client, a pioneering pharmaceutical company, is seeking a distinguished Principal Pharmaceutical Scientist to lead groundbreaking research and development initiatives. This is a fully remote position, offering an exceptional opportunity for a seasoned scientist to contribute to the discovery and development of novel therapeutics from their home office. The ideal candidate will possess extensive expertise in medicinal chemistry, pharmacology, or a related discipline, with a strong publication record and a history of successfully advancing drug candidates through the preclinical pipeline.
Responsibilities:
Responsibilities:
- Lead and direct research projects focused on identifying and validating novel drug targets and developing innovative small molecule or biologic drug candidates.
- Design, synthesize, and characterize novel chemical entities with therapeutic potential.
- Conduct rigorous preclinical studies, including in vitro and in vivo pharmacology, toxicology, and pharmacokinetic assessments.
- Develop and optimize drug delivery systems and formulation strategies.
- Collaborate effectively with a globally distributed, remote team of chemists, biologists, pharmacologists, and clinicians.
- Analyze and interpret complex experimental data, providing strategic direction for drug discovery programs.
- Author scientific publications, patents, and regulatory documents.
- Mentor and guide junior scientists, fostering a collaborative and innovative research environment.
- Stay at the forefront of scientific advancements in relevant therapeutic areas and drug discovery technologies.
- Contribute to the strategic planning and portfolio management of drug development projects, considering various markets including Embu, Embu, KE , for future commercialization.
- Manage external collaborations with academic institutions and contract research organizations (CROs).
- Ph.D. in Medicinal Chemistry, Pharmacology, Pharmaceutical Sciences, or a closely related field.
- Minimum of 10 years of relevant industry experience in drug discovery and preclinical development.
- Demonstrated expertise in a specific therapeutic area (e.g., oncology, infectious diseases, CNS disorders).
- Strong understanding of drug metabolism and pharmacokinetics (DMPK), toxicology, and regulatory requirements for drug development.
- Proven track record of successfully leading drug discovery projects and advancing candidates into clinical trials.
- Excellent scientific judgment, critical thinking, and problem-solving skills.
- Exceptional written and verbal communication skills, essential for remote collaboration and scientific dissemination.
- Experience with scientific literature databases (e.g., SciFinder, PubMed) and data analysis software.
- Ability to work independently and manage multiple research projects concurrently in a remote setting.
- A strong publication record in peer-reviewed journals and relevant patent filings is highly advantageous.
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Clinical Research Scientist - Drug Development
Posted 21 days ago
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Job Description
Our client, a leading pharmaceutical company dedicated to advancing human health, is seeking an accomplished Clinical Research Scientist to join their innovative drug development team. This is a fully remote position, offering you the flexibility to contribute your scientific expertise from anywhere in Kenya, with a focus on research activities relevant to the **Nyeri, Nyeri, KE** region and its scientific community. You will play a pivotal role in the design, execution, and interpretation of clinical trials for novel therapeutic agents. Key responsibilities include developing clinical trial protocols, overseeing study conduct, ensuring data integrity, and analyzing study results to support regulatory submissions and publication. You will collaborate closely with internal R&D departments, external investigators, contract research organizations (CROs), and regulatory authorities. The ideal candidate possesses a Ph.D. or M.D. in a relevant life science discipline, with a minimum of 5 years of experience in clinical research and drug development within the pharmaceutical or biotechnology industry. A deep understanding of clinical trial methodologies, regulatory guidelines (e.g., ICH-GCP), and statistical analysis is essential. Strong scientific acumen, excellent written and verbal communication skills, and the ability to critically evaluate scientific data are paramount. Experience in a specific therapeutic area relevant to the company's pipeline is a significant advantage. We are looking for a highly motivated, detail-oriented individual who can independently manage complex research projects, drive scientific innovation, and contribute to the development of life-changing medicines. This role offers a unique opportunity to engage in cutting-edge pharmaceutical research and contribute to the global effort of bringing new therapies to patients in need.
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Principal Scientist - Drug Discovery & Development
Posted 14 days ago
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Job Description
Our client, a pioneering pharmaceutical research organization, is looking for a highly accomplished Principal Scientist to lead critical initiatives within our drug discovery and development pipeline. This is a fully remote position, enabling top-tier scientific talent to contribute from anywhere in the world. The ideal candidate will possess a strong track record in innovative pharmaceutical research, with expertise in one or more key therapeutic areas. You will play a pivotal role in identifying, validating, and advancing novel drug candidates from early-stage research through to pre-clinical development.
Key Responsibilities:
Qualifications:
Key Responsibilities:
- Design and execute innovative research strategies to identify and validate novel drug targets and therapeutic candidates.
- Lead projects focused on small molecule or biologic drug discovery, from hit identification to lead optimization.
- Develop and implement cutting-edge assays and experimental methodologies relevant to target validation and compound screening.
- Analyze complex biological data, interpret results, and make informed decisions to advance research programs.
- Collaborate closely with internal teams (e.g., medicinal chemistry, pharmacology, DMPK) and external partners to drive project progression.
- Provide scientific leadership and mentorship to research associates and junior scientists in a remote environment.
- Prepare high-quality scientific reports, publications, and presentations for internal review and external dissemination.
- Contribute to the strategic direction of the R&D pipeline and identify new opportunities for innovation.
- Ensure all research activities are conducted in compliance with ethical standards and regulatory guidelines.
Qualifications:
- Ph.D. in Molecular Biology, Biochemistry, Pharmacology, or a related life science discipline.
- Minimum of 10 years of post-doctoral and/or industry experience in pharmaceutical drug discovery.
- Demonstrated expertise in a specific therapeutic area (e.g., oncology, immunology, neuroscience) and/or a specific modality (e.g., small molecules, biologics, gene therapy).
- Proven track record of successfully progressing drug candidates through discovery and pre-clinical development.
- Extensive experience with various molecular and cellular biology techniques, assay development, and high-throughput screening.
- Strong understanding of drug metabolism, pharmacokinetics (DMPK), and toxicology principles.
- Excellent analytical, critical thinking, and problem-solving skills.
- Exceptional written and verbal communication skills, with a talent for scientific storytelling.
- Ability to lead research projects, mentor junior scientists, and collaborate effectively in a remote, cross-functional team setting.
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Remote Principal Scientist - Drug Discovery & Development
Posted 7 days ago
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Job Description
Our client, a world-renowned pharmaceutical research institution, is seeking a distinguished and highly experienced Remote Principal Scientist to lead critical initiatives in drug discovery and development. This is an entirely remote position, offering an exceptional opportunity to make significant contributions to medicinal advancements from your home-based laboratory or research setup. You will be responsible for designing and executing complex research programs, identifying novel therapeutic targets, developing preclinical drug candidates, and guiding multidisciplinary research teams. The ideal candidate possesses a Ph.D. in Pharmacology, Medicinal Chemistry, or a related discipline, a substantial track record of successful drug development, strong leadership capabilities, and extensive experience in guiding research from discovery through early clinical stages. You will play a pivotal role in shaping the company's R&D pipeline and advancing life-saving treatments.
Responsibilities:
Responsibilities:
- Lead and direct cutting-edge research programs focused on identifying and validating novel drug targets.
- Design and oversee the synthesis and optimization of small molecule drug candidates.
- Develop and implement robust preclinical study designs to assess drug efficacy, safety, and pharmacokinetics.
- Interpret complex experimental data and guide research strategies for progression.
- Mentor and manage a team of scientists and research associates, fostering a collaborative and innovative environment.
- Collaborate effectively with internal and external partners, including CROs and academic institutions.
- Contribute significantly to the preparation of regulatory submissions and intellectual property filings.
- Stay at the forefront of scientific advancements in relevant therapeutic areas and drug discovery technologies.
- Present research findings and strategic plans to senior management and scientific advisory boards.
- Ensure compliance with all relevant ethical, safety, and regulatory guidelines.
- Ph.D. in Pharmacology, Medicinal Chemistry, Biochemistry, or a closely related field.
- Minimum of 10 years of progressive experience in drug discovery and development within the pharmaceutical or biotechnology industry.
- Demonstrated success in advancing drug candidates from discovery through preclinical development.
- In-depth knowledge of drug target identification, validation, and lead optimization strategies.
- Extensive experience with various assay development, screening technologies, and preclinical models.
- Strong leadership, team management, and interpersonal skills.
- Exceptional analytical, critical thinking, and problem-solving abilities.
- Excellent written and verbal communication skills, adept at remote scientific discourse and reporting.
- Proven ability to manage complex research projects, budgets, and timelines in a remote setting.
- A deep understanding of the pharmaceutical R&D landscape and regulatory requirements.
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