674 Remote Pharmaceutical Research Associate jobs in Kenya
Remote Pharmaceutical Quality Control Analyst (Trainee)
Posted 13 days ago
Job Viewed
Job Description
Remote Pharmaceutical Research Associate
Posted 20 days ago
Job Viewed
Job Description
Your Responsibilities Will Include:
- Designing and conducting laboratory experiments or in-silico studies related to drug discovery and development.
- Collecting, analyzing, and interpreting complex research data using statistical software and bioinformatics tools.
- Preparing detailed research reports, manuscripts for publication, and presentations.
- Collaborating with cross-functional teams, including chemists, biologists, and clinicians, in a virtual environment.
- Maintaining accurate and organized records of experimental procedures, results, and observations.
- Ensuring compliance with all relevant regulatory guidelines and company SOPs.
- Troubleshooting experimental issues and developing innovative solutions.
- Contributing to the development of new research methodologies and protocols.
- Staying abreast of the latest scientific literature and advancements in pharmaceutical sciences.
- Presenting research findings at virtual scientific conferences or internal meetings.
- Master's degree or Ph.D. in Pharmacology, Biochemistry, Molecular Biology, Chemistry, or a related life science field.
- Proven experience in pharmaceutical research, with a strong understanding of drug development processes.
- Proficiency in relevant research techniques and methodologies (e.g., cell culture, PCR, Western blotting, chromatography, molecular modeling).
- Strong analytical skills and experience with statistical analysis and data interpretation.
- Excellent written and verbal communication skills, essential for remote collaboration.
- Ability to work independently with minimal supervision and manage multiple projects simultaneously.
- Proficiency in relevant software (e.g., GraphPad Prism, R, Python, Schrödinger Suite).
- A meticulous approach to record-keeping and experimental execution.
- Demonstrated ability to critically evaluate scientific data and draw sound conclusions.
- Experience with regulatory affairs and Good Laboratory Practice (GLP) is a plus.
Remote Graduate Trainee - Pharmaceutical Research
Posted 20 days ago
Job Viewed
Job Description
Program Features:
- Participate in ongoing pharmaceutical research projects, contributing to various stages of the R&D process.
- Assist in designing and conducting experiments, collecting and analyzing research data.
- Learn and apply standard laboratory techniques and protocols in a virtual context.
- Prepare research reports, presentations, and scientific documentation.
- Support senior researchers in literature reviews and data interpretation.
- Gain exposure to drug discovery, preclinical studies, and clinical trial support processes.
- Understand and adhere to Good Laboratory Practice (GLP) and other relevant regulatory guidelines.
- Collaborate with cross-functional teams, including scientists, statisticians, and regulatory affairs specialists.
- Utilize scientific databases and research tools for data mining and analysis.
- Contribute to the development of new research methodologies and protocols.
- Attend virtual seminars and training sessions to enhance scientific knowledge and skills.
- Develop critical thinking and problem-solving skills in a scientific research setting.
Eligibility:
- Recent graduate with a Bachelor's or Master's degree in Pharmacy, Chemistry, Biology, Biotechnology, Pharmacology, or a related life science field.
- Strong academic record and a foundational understanding of scientific principles.
- Genuine interest in pharmaceutical research and drug development.
- Excellent analytical and quantitative skills.
- Strong written and verbal communication abilities.
- Ability to work independently, manage time effectively, and maintain focus in a remote environment.
- Detail-oriented with a commitment to accuracy and scientific integrity.
- Proficiency in Microsoft Office Suite (Word, Excel, PowerPoint).
- Experience with scientific literature databases is a plus.
- Must be legally authorized to work in Kenya and have reliable internet access.
Senior Clinical Research Associate - Pharmaceuticals (Remote)
Posted 20 days ago
Job Viewed
Job Description
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).
Senior Quality Control Analyst (Pharmaceuticals) - Remote
Posted 18 days ago
Job Viewed
Job Description
Key Responsibilities:
- Develop, validate, and optimize analytical methods for raw materials, in-process samples, and finished pharmaceutical products using techniques such as HPLC, GC, spectroscopy, and titrimetry.
- Perform routine quality control testing according to established protocols and specifications.
- Analyze and interpret test results, identifying any deviations or out-of-specification (OOS) findings.
- Investigate OOS results, implement corrective and preventive actions (CAPAs), and document all findings thoroughly.
- Ensure compliance with Good Manufacturing Practices (GMP), Good Laboratory Practices (GLP), and relevant regulatory guidelines (e.g., FDA, EMA).
- Maintain and calibrate laboratory equipment, ensuring its proper functioning and adherence to calibration schedules.
- Prepare Certificates of Analysis (CoA) and other quality-related documentation.
- Participate in internal and external audits, providing necessary information and demonstrating compliance.
- Train and mentor junior QC analysts on analytical techniques, procedures, and compliance requirements.
- Contribute to continuous improvement initiatives within the Quality Control department.
Qualifications:
- Bachelor's or Master's degree in Chemistry, Pharmaceutical Sciences, or a related field.
- A minimum of 5 years of experience in pharmaceutical quality control, with a strong understanding of analytical techniques.
- Extensive hands-on experience with analytical instrumentation (HPLC, GC, UV-Vis, FTIR, etc.).
- In-depth knowledge of GMP, GLP, and regulatory requirements for pharmaceutical manufacturing.
- Proven experience in method validation and OOS investigations.
- Strong analytical, problem-solving, and critical thinking skills.
- Excellent attention to detail and organizational abilities.
- Proficiency in documentation and report writing.
- Ability to work independently and manage workload effectively in a remote environment.
- Familiarity with pharmaceutical manufacturing processes relevant to **Kakamega, Kakamega, KE** or similar regions is a plus.
Quality Control Analyst (Pharmaceutical)
Posted 20 days ago
Job Viewed
Job Description
Responsibilities:
- Conduct routine and non-routine analytical testing of raw materials, in-process samples, and finished pharmaceutical products using various analytical techniques (e.g., HPLC, GC, UV-Vis Spectroscopy, Titration).
- Prepare reagents, solutions, and standards required for testing.
- Maintain accurate and detailed laboratory records, documenting all procedures, results, and observations in compliance with Good Laboratory Practices (GLP) and Good Manufacturing Practices (GMP).
- Calibrate and maintain laboratory equipment, ensuring proper functioning and adherence to calibration schedules.
- Investigate out-of-specification (OOS) results, identify root causes, and participate in deviation investigations.
- Assist in the validation and transfer of analytical methods.
- Review and approve testing data and reports.
- Stay informed about current pharmacopeial methods (e.g., USP, BP, EP) and relevant regulatory guidelines.
- Participate in internal and external audits as required.
- Contribute to the continuous improvement of quality control processes and procedures.
- Bachelor's degree in Chemistry, Biochemistry, Pharmacy, or a related scientific field.
- Minimum of 3 years of experience in a pharmaceutical quality control or analytical laboratory setting.
- Proficiency in operating and maintaining analytical instrumentation, particularly HPLC and GC.
- Solid understanding of GMP, GLP, and relevant regulatory requirements.
- Experience with pharmacopeial testing and monographs.
- Strong problem-solving skills and ability to troubleshoot analytical issues.
- Excellent attention to detail and accuracy in data recording and analysis.
- Good organizational and time management skills.
- Effective written and verbal communication abilities.
- Ability to work independently and collaboratively in a hybrid environment, balancing remote tasks with essential on-site laboratory duties.
Principal Pharmaceutical Scientist, Drug Discovery
Posted 20 days ago
Job Viewed
Job Description
- Leading and directing research projects focused on the discovery and optimization of novel drug candidates.
- Designing and implementing innovative experimental strategies to address complex biological and chemical challenges.
- Conducting in-depth analysis of experimental data, interpreting results, and making data-driven recommendations.
- Mentoring and guiding a team of research scientists, fostering a culture of scientific rigor and collaboration.
- Collaborating closely with cross-functional teams, including biologists, toxicologists, and clinical development scientists.
- Staying abreast of the latest scientific advancements and emerging technologies in drug discovery.
- Contributing to the development of intellectual property and preparing scientific publications and presentations.
- Evaluating potential drug targets and developing hit-to-lead and lead optimization programs.
- Managing external research collaborations and partnerships.
- Ensuring compliance with all relevant safety and ethical guidelines in research conduct.
Be The First To Know
About the latest Remote pharmaceutical research associate Jobs in Kenya !
Principal Scientist - Biotechnology Research
Posted 17 days ago
Job Viewed
Job Description
Principal Pharmaceutical Scientist, Drug Discovery (Remote)
Posted 20 days ago
Job Viewed
Job Description
Senior Pharmaceutical Scientist - Drug Discovery
Posted 20 days ago
Job Viewed
Job Description
Key Responsibilities:
- Design and synthesize novel small molecules with therapeutic potential.
- Conduct in vitro and in vivo assays to evaluate drug efficacy and safety.
- Perform DMPK studies to characterize drug absorption, distribution, metabolism, and excretion.
- Optimize lead compounds through medicinal chemistry efforts.
- Collaborate with biologists and pharmacologists to define and validate drug targets.
- Develop and execute experimental plans for drug discovery projects.
- Analyze and interpret complex scientific data, generating high-quality reports.
- Stay abreast of the latest scientific literature and technological advancements in drug discovery.
- Mentor and guide junior scientists, fostering a collaborative research environment.
- Ensure adherence to laboratory safety regulations and best practices.
- Contribute to the strategic planning of the drug discovery portfolio.
The ideal candidate will hold a Ph.D. in Medicinal Chemistry, Organic Chemistry, Pharmacology, or a related field, with a minimum of 7-9 years of postdoctoral and/or industry experience in drug discovery. Proven experience in small molecule synthesis, structure-activity relationship (SAR) analysis, and hit-to-lead optimization is mandatory. Proficiency with modern analytical techniques (e.g., LC-MS, NMR) and biological assay development is required. A strong understanding of pharmacology, pharmacokinetics, and drug development processes is essential. Excellent scientific judgment, problem-solving abilities, and strong written and verbal communication skills are necessary. The ability to work effectively in a fully remote research setting is a must. This role is fully remote, supporting critical research that could impact therapeutic development for conditions relevant to populations potentially near Naivasha, Nakuru, KE , and beyond.