756 Medical Research jobs in Bahrain

Senior Bio-Medical Research Scientist

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1007 Seef, Capital BHD75000 Annually WhatJobs

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full-time
Our client, a pioneering biotechnology firm, is seeking a highly motivated and experienced Senior Bio-Medical Research Scientist to join their esteemed R&D team. The successful candidate will play a pivotal role in designing, executing, and analyzing complex experiments aimed at developing novel therapeutic agents. This position is based in our state-of-the-art laboratory facilities located in Janabiyah, Northern, BH .

Responsibilities will include:
  • Conceptualizing and developing innovative research protocols and methodologies.
  • Conducting in-depth literature reviews to stay abreast of the latest scientific advancements.
  • Designing and executing experiments related to molecular biology, cell culture, protein expression, and purification.
  • Analyzing experimental data using advanced statistical methods and presenting findings to cross-functional teams.
  • Troubleshooting experimental issues and optimizing protocols to ensure data integrity and reproducibility.
  • Mentoring junior researchers and providing technical guidance.
  • Collaborating with external partners and academic institutions to foster innovation and knowledge sharing.
  • Ensuring compliance with all laboratory safety regulations and ethical guidelines.
  • Contributing to the preparation of grant proposals and scientific publications.
  • Managing laboratory resources and maintaining detailed experimental records.

The ideal candidate will possess a Ph.D. in Molecular Biology, Biochemistry, or a related life science discipline, with a minimum of 5 years of post-doctoral research experience in a relevant field. Demonstrated expertise in CRISPR-Cas9 gene editing, mammalian cell culture techniques, and protein-ligand binding assays is essential. Strong analytical and problem-solving skills, coupled with excellent written and verbal communication abilities, are required. The ability to work independently as well as part of a dynamic team is crucial. Experience with bioinformatics tools and data analysis software is a significant advantage. Familiarity with regulatory affairs pertaining to drug development is also desirable. This is an exceptional opportunity for a dedicated scientist eager to make a significant impact on human health.
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Senior Scientific Research Scientist - Biotechnology

New
422 Al Markh BHD70000 Annually WhatJobs

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full-time
Our client, a pioneering biotechnology research and development firm, is seeking a highly accomplished Senior Scientific Research Scientist with expertise in Biotechnology to contribute to groundbreaking advancements in Sanad, Capital, BH . This pivotal role involves leading research projects, designing experiments, analyzing complex biological data, and contributing to the development of innovative biotechnological solutions.

Key Responsibilities:
  • Design, conduct, and optimize experiments related to molecular biology, cell biology, protein engineering, or related biotechnological fields.
  • Develop and validate new research methodologies and techniques.
  • Analyze and interpret complex scientific data using statistical software and bioinformatics tools.
  • Write and present research findings at scientific conferences and in peer-reviewed publications.
  • Collaborate with cross-functional teams, including other scientists, engineers, and project managers, to advance research projects.
  • Oversee laboratory operations, ensuring compliance with safety protocols and regulatory standards.
  • Manage research projects, including planning, resource allocation, and timeline management.
  • Mentor and guide junior research associates and scientists.
  • Identify and pursue new research opportunities and funding avenues.
  • Maintain comprehensive and accurate laboratory notebooks and documentation.
Qualifications:
  • Ph.D. in Biotechnology, Molecular Biology, Biochemistry, Genetics, or a related life science discipline.
  • Minimum of 5 years of post-doctoral research experience in a relevant biotechnology field.
  • Demonstrated expertise in experimental design, data analysis, and scientific interpretation.
  • Proficiency in a range of laboratory techniques relevant to biotechnology (e.g., PCR, Western blotting, ELISA, flow cytometry, CRISPR, recombinant protein expression).
  • Experience with bioinformatics tools and databases is highly desirable.
  • Strong publication record in reputable scientific journals.
  • Excellent written and verbal communication skills, with the ability to articulate complex scientific concepts clearly.
  • Proven leadership and project management skills.
  • Ability to work independently and collaboratively in a team-oriented research environment.
  • Strong critical thinking and problem-solving abilities.
This is an exceptional opportunity for a seasoned scientist to make a significant contribution to cutting-edge research and development. If you are passionate about innovation and possess the required expertise, we invite you to join our client's world-class scientific team.
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Senior Research Scientist, Medical Devices

New
431 Seef, Capital BHD140000 Annually WhatJobs

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full-time
Our client is seeking a highly experienced Senior Research Scientist with expertise in Medical Devices to drive innovation and development in Janabiyah, Northern, BH . This pivotal role involves leading the research and development of next-generation medical technologies, from concept ideation through to prototype development and validation. You will be responsible for defining research objectives, designing experimental protocols, and executing studies to evaluate device performance, safety, and efficacy. Key responsibilities include collaborating with engineering, clinical, and regulatory affairs teams to ensure successful product development lifecycle management. The Senior Research Scientist will analyze research data, interpret results, and prepare comprehensive technical reports and presentations for internal stakeholders and regulatory submissions. You will also mentor junior scientists and contribute to the strategic direction of the R&D department. A strong foundation in biomedical engineering, materials science, or a related field is essential, coupled with a proven track record in medical device research and development. Experience with various medical device technologies, including diagnostics, therapeutic devices, or implantable systems, is highly valued. Proficiency in relevant laboratory techniques, prototyping tools, and data analysis software is required. The ideal candidate will possess exceptional analytical, problem-solving, and project management skills, with excellent scientific communication abilities. Familiarity with regulatory pathways for medical devices (e.g., FDA, CE marking) is a significant advantage. We are looking for an innovative thinker with a passion for improving patient outcomes through cutting-edge medical technology. This is an outstanding opportunity to contribute to the advancement of healthcare and shape the future of medical devices. Your expertise will be instrumental in bringing life-changing innovations to market.
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Clinical Research Scientist

10256 Busaiteen, Muharraq BHD75000 Annually WhatJobs

Posted 1 day ago

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full-time
Our client, a leading pharmaceutical research and development company situated in Busaiteen, Muharraq, BH , is seeking a highly skilled and dedicated Clinical Research Scientist. This role is critical to advancing our pipeline of innovative therapeutics through meticulous planning, execution, and analysis of clinical trials. The ideal candidate will possess a strong scientific background, extensive experience in clinical research methodologies, and a commitment to upholding the highest standards of data integrity and regulatory compliance. You will contribute to groundbreaking studies that have the potential to transform patient care.

Responsibilities:
  • Design and develop clinical trial protocols, ensuring scientific validity and alignment with regulatory requirements.
  • Oversee the operational aspects of clinical trials, including site selection, initiation, monitoring, and close-out.
  • Collaborate with cross-functional teams, including medical affairs, regulatory affairs, data management, and biostatistics.
  • Analyze clinical trial data, interpret results, and prepare comprehensive study reports.
  • Contribute to the writing of regulatory submission documents (e.g., INDs, NDAs) and scientific publications.
  • Ensure compliance with Good Clinical Practice (GCP), FDA regulations, and other relevant guidelines.
  • Manage external collaborations with clinical sites, investigators, and contract research organizations (CROs).
  • Develop and present scientific findings at internal meetings and external conferences.
  • Stay current with scientific literature, emerging technologies, and therapeutic area advancements.
  • Contribute to the strategy and planning of future clinical development programs.
  • Ensure the safety and well-being of study participants throughout the trial lifecycle.
Qualifications:
  • Ph.D. or equivalent doctoral degree in a relevant life science, biomedical science, or related field.
  • Minimum of 5 years of experience in clinical research, with a focus on clinical trial design and execution within the pharmaceutical industry.
  • Strong understanding of drug development processes, clinical trial phases, and regulatory pathways.
  • Proven experience in data analysis, interpretation, and scientific writing.
  • Excellent knowledge of GCP, ICH guidelines, and regulatory submission requirements.
  • Demonstrated ability to manage complex projects and cross-functional teams.
  • Strong analytical, problem-solving, and critical thinking skills.
  • Effective communication and presentation skills, with the ability to convey complex scientific information clearly.
  • Experience in therapeutic areas such as oncology, immunology, or cardiovascular diseases is highly desirable.
  • Ability to work independently and as part of a collaborative team in a fast-paced environment.
This is an outstanding opportunity to contribute to cutting-edge pharmaceutical research in a supportive and intellectually stimulating environment.
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Clinical Research Scientist

10321 Seef, Capital BHD90000 Annually WhatJobs

Posted 5 days ago

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full-time
Our client, a leading pharmaceutical company, is seeking a highly motivated and analytical Clinical Research Scientist to join their team in Janabiyah, Northern, BH . This role is pivotal in advancing groundbreaking research and developing innovative pharmaceutical products. You will be responsible for designing, implementing, and managing clinical trials, analyzing research data, and ensuring compliance with regulatory standards and ethical guidelines. The ideal candidate will have a strong scientific background, excellent understanding of clinical research methodologies, and proficiency in data analysis software. Key responsibilities include protocol development, subject recruitment strategy, data collection and management, statistical analysis, and report writing. You will collaborate closely with cross-functional teams, including medical affairs, regulatory affairs, and marketing. A Ph.D. or Master's degree in Life Sciences, Pharmacology, or a related field is required, along with a minimum of 5 years of experience in clinical research within the pharmaceutical industry. Experience with various therapeutic areas and a deep understanding of Good Clinical Practice (GCP) and FDA regulations are essential. Strong critical thinking, problem-solving, and communication skills are necessary. This is an exciting opportunity to make a significant contribution to patient health by driving the development of new medicines.
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Clinical Research Scientist - Oncology

30685 Northern, Northern BHD95000 Annually WhatJobs

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full-time
Our client is searching for a highly qualified and dedicated Clinical Research Scientist specializing in Oncology to join their cutting-edge pharmaceutical research division in Shakhura, Northern, BH . This role is integral to the advancement of novel cancer therapies, contributing significantly to the drug development lifecycle. The successful candidate will be responsible for designing, executing, and analyzing clinical trials, with a primary focus on oncological treatments. Key responsibilities include developing clinical trial protocols, identifying and recruiting eligible patients, managing trial data, ensuring compliance with Good Clinical Practice (GCP) guidelines and regulatory requirements, collaborating with cross-functional teams (including medical affairs, regulatory affairs, and data management), preparing scientific reports and publications, and presenting findings at internal and external meetings. A Ph.D. or M.D. in a relevant life science field (e.g., pharmacology, oncology, molecular biology) is required, along with substantial experience in clinical trial management, particularly in oncology. Excellent scientific knowledge, strong analytical skills, and a deep understanding of cancer biology and therapeutic approaches are essential. The ability to work effectively in a fast-paced, collaborative environment and to communicate complex scientific information clearly is paramount. This is an exceptional opportunity to contribute to life-saving medical advancements and grow your career within a leading pharmaceutical organization. If you are passionate about advancing cancer care through rigorous scientific research, we encourage you to apply.
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Clinical Research Scientist - Oncology

20191 Seef, Capital BHD75000 Annually WhatJobs

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full-time
Our client, a leading pharmaceutical innovator, is actively recruiting a highly motivated Clinical Research Scientist specializing in Oncology for their facility in **Janabiyah, Northern, BH**. This senior-level position will play a critical role in the design, execution, and analysis of clinical trials for novel cancer therapies. The successful candidate will be responsible for developing study protocols, overseeing patient recruitment, managing data integrity, and ensuring compliance with regulatory guidelines (e.g., ICH-GCP). You will collaborate closely with cross-functional teams, including medical affairs, regulatory affairs, and clinical operations, as well as external investigators and research sites. Key responsibilities include interpreting clinical data, preparing regulatory submissions, and contributing to scientific publications and presentations. A Ph.D. or M.D. in a relevant scientific discipline (e.g., Oncology, Pharmacology, Molecular Biology) is mandatory, coupled with a minimum of 7 years of progressive experience in clinical research within the pharmaceutical or biotechnology industry, with a strong focus on oncology. Excellent understanding of cancer biology, drug development processes, and regulatory requirements is essential. Demonstrated success in managing complex clinical trials and a strong publication record are highly desirable. This role requires exceptional analytical, problem-solving, and communication skills. The ability to lead and mentor junior staff is also important. Our client is committed to advancing cancer treatment and offers a stimulating research environment with state-of-the-art facilities. This is an outstanding opportunity to contribute to life-saving medical advancements in a key therapeutic area. The ideal candidate will be passionate about oncology research and possess a strategic mindset to drive successful trial outcomes.
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Senior Clinical Research Scientist

22210 Hamad Town, Northern BHD110000 Annually WhatJobs

Posted 1 day ago

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full-time
Our client, a leading pharmaceutical innovator, is actively searching for an accomplished Senior Clinical Research Scientist to contribute to groundbreaking advancements in drug development. This exciting opportunity is based in Hamad Town, Northern, BH . The successful candidate will play a critical role in the design, execution, and interpretation of clinical trials, focusing on novel therapeutic areas. You will be responsible for developing study protocols, overseeing the clinical trial process, managing data analysis, and ensuring compliance with regulatory guidelines and Good Clinical Practice (GCP). Key responsibilities include collaborating with cross-functional teams such as regulatory affairs, biostatistics, and medical affairs; providing scientific and medical input into study design and implementation; managing relationships with investigators and clinical sites; analyzing and interpreting clinical data; and preparing scientific publications and presentations. A Ph.D. or M.D. in a life science discipline (e.g., Pharmacology, Medicine, Biology) is required, along with a minimum of 7 years of experience in clinical research within the pharmaceutical or biotechnology industry. Demonstrated experience in designing and conducting Phase I-IV clinical trials, along with a strong understanding of regulatory requirements (FDA, EMA), is essential. Excellent analytical, problem-solving, and critical thinking skills are a must. The ability to communicate complex scientific information clearly and effectively to both technical and non-technical audiences is paramount. You should possess strong project management skills and the ability to lead and mentor junior researchers. Familiarity with common statistical software and clinical trial management systems is highly desirable. This role offers the chance to make a significant impact on patient lives by bringing innovative medicines to market.

  • Lead the design and development of clinical trial protocols.
  • Oversee the execution of clinical trials, ensuring adherence to timelines and budgets.
  • Analyze and interpret complex clinical trial data to assess drug efficacy and safety.
  • Collaborate with regulatory affairs and health authorities to ensure compliance.
  • Prepare clinical study reports, manuscripts for publication, and regulatory submissions.
  • Manage relationships with investigators, study coordinators, and clinical research organizations (CROs).
  • Provide scientific expertise and guidance to clinical development teams.
  • Evaluate and interpret safety data and implement risk management strategies.

We are looking for a passionate scientist eager to contribute to cutting-edge pharmaceutical research.
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Clinical Research Scientist (Oncology)

20150 Amwaj Islands BHD95000 Annually WhatJobs

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full-time
Our client is seeking a dedicated and experienced Clinical Research Scientist specializing in Oncology to join their pioneering pharmaceutical research team in Isa Town, Southern, BH . This critical role will involve the design, execution, and analysis of clinical trials aimed at developing novel cancer therapies. The successful candidate will be instrumental in advancing our understanding of cancer biology and translating scientific discoveries into life-saving treatments. Responsibilities include developing clinical trial protocols, identifying and evaluating potential study sites and investigators, and overseeing patient recruitment and data collection. You will be responsible for ensuring that all clinical research activities are conducted in strict accordance with regulatory guidelines (e.g., ICH-GCP) and ethical standards. The Clinical Research Scientist will work closely with cross-functional teams, including medical affairs, regulatory affairs, and biostatistics, to ensure the successful progression of clinical programs. Strong scientific acumen, a deep understanding of oncology, and experience in clinical trial management are essential. The ability to critically evaluate scientific literature, interpret complex data, and contribute to the preparation of regulatory submission documents is also crucial. We are looking for a motivated individual with a passion for scientific innovation and a commitment to improving patient outcomes. This position offers a challenging and rewarding opportunity to contribute to the development of breakthrough cancer therapies.

Responsibilities:
  • Design and develop clinical trial protocols for oncology studies.
  • Identify and assess potential clinical investigators and sites.
  • Oversee the execution of clinical trials, ensuring compliance with GCP and regulations.
  • Monitor study progress, data quality, and patient safety.
  • Analyze clinical trial data and interpret study results.
  • Prepare clinical study reports and contribute to regulatory submissions.
  • Collaborate with internal and external stakeholders, including medical monitors and statisticians.
  • Stay abreast of the latest advancements in oncology research and drug development.
  • Manage budgets and timelines for clinical trials.
  • Ensure effective communication among study teams and investigators.

Qualifications:
  • Ph.D. or M.D. in a relevant scientific discipline (e.g., Molecular Biology, Pharmacology, Medicine).
  • Minimum of 5 years of experience in clinical research, preferably in oncology.
  • Thorough understanding of clinical trial design and methodology.
  • In-depth knowledge of oncology drug development and cancer biology.
  • Familiarity with ICH-GCP guidelines and regulatory requirements.
  • Strong analytical and data interpretation skills.
  • Excellent written and verbal communication skills.
  • Ability to manage complex projects and multiple tasks.
  • Experience with data management systems and statistical analysis software.
  • Strong problem-solving abilities and attention to detail.
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Senior Clinical Research Scientist

56789 Durrat Al Bahrain BHD95000 Annually WhatJobs

Posted 5 days ago

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full-time
Our client, a pioneering pharmaceutical company dedicated to advancing healthcare solutions, is seeking a highly qualified Senior Clinical Research Scientist to join their innovative team in **Jidhafs, Capital, BH**. This vital role will involve contributing to the design, execution, and analysis of clinical trials for groundbreaking new therapies. You will be responsible for developing study protocols, overseeing data collection, and ensuring compliance with regulatory guidelines (e.g., ICH-GCP). The ideal candidate will possess a strong scientific background, a deep understanding of clinical trial methodologies, and excellent analytical skills. Collaboration with investigators, clinical research associates (CRAs), and regulatory affairs teams will be integral to the success of the studies. Your expertise will be crucial in interpreting complex data, identifying trends, and contributing to regulatory submissions. Responsibilities include:
  • Designing and developing clinical trial protocols and associated documents.
  • Overseeing the operational aspects of clinical trials, ensuring adherence to protocols and timelines.
  • Monitoring study progress, data quality, and patient safety.
  • Analyzing clinical data and contributing to the interpretation of results.
  • Preparing study reports, manuscripts for publication, and regulatory submission documents.
  • Ensuring compliance with all applicable regulatory requirements and ethical standards.
  • Collaborating with external investigators and study sites to ensure efficient trial conduct.
  • Providing scientific and technical expertise to the clinical development team.
  • Staying abreast of scientific literature and advancements in relevant therapeutic areas.
Qualifications:
  • Ph.D. or Master's degree in a relevant scientific discipline (e.g., Pharmacology, Biomedical Sciences, Pharmacy).
  • Minimum of 5 years of experience in clinical research within the pharmaceutical or biotechnology industry.
  • In-depth knowledge of clinical trial design, execution, and data analysis.
  • Familiarity with ICH-GCP guidelines and other relevant regulatory requirements.
  • Strong critical thinking and problem-solving abilities.
  • Excellent written and verbal communication skills.
  • Ability to manage multiple projects simultaneously and meet deadlines.
  • Experience in specific therapeutic areas is a plus.
This is an exceptional opportunity to contribute to the development of life-changing medicines and to grow your career within a supportive and cutting-edge research environment.
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