1 954 Drug Development jobs in Bahrain
Clinical Research Associate (Drug Development)
78901 Al Muharraq
BHD85000 Annually
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Posted 2 days ago
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Job Description
Our client, a dynamic pharmaceutical company at the forefront of medical innovation, is actively seeking a skilled Clinical Research Associate (CRA) to join their team. This role is critical to the successful execution of clinical trials, ensuring the safety of participants and the integrity of data for novel drug development programs. The position is based at our state-of-the-art facility in Sitra, Capital, BH .
As a CRA, you will be responsible for monitoring clinical trial sites to ensure adherence to study protocols, regulatory requirements (e.g., GCP, FDA regulations), and company policies. This involves conducting site visits (pre-study, initiation, interim monitoring, and close-out), assessing the quality of trial conduct, and verifying the accuracy and completeness of source data and case report forms (CRFs). You will serve as the primary point of contact for study sites, providing training to investigators and site staff on study-related matters, and resolving any site-level issues that may arise. Data management is a key component, ensuring that all data is collected, reviewed, and reported in a timely and accurate manner. You will also be involved in regulatory document review, study budget management, and liaising with various internal departments, including data management, biostatistics, and regulatory affairs. The successful candidate will possess a strong understanding of clinical trial processes, excellent communication and interpersonal skills, and the ability to travel to clinical sites as needed. A meticulous approach to work and a commitment to maintaining the highest standards of research ethics are essential.
Key Responsibilities:
As a CRA, you will be responsible for monitoring clinical trial sites to ensure adherence to study protocols, regulatory requirements (e.g., GCP, FDA regulations), and company policies. This involves conducting site visits (pre-study, initiation, interim monitoring, and close-out), assessing the quality of trial conduct, and verifying the accuracy and completeness of source data and case report forms (CRFs). You will serve as the primary point of contact for study sites, providing training to investigators and site staff on study-related matters, and resolving any site-level issues that may arise. Data management is a key component, ensuring that all data is collected, reviewed, and reported in a timely and accurate manner. You will also be involved in regulatory document review, study budget management, and liaising with various internal departments, including data management, biostatistics, and regulatory affairs. The successful candidate will possess a strong understanding of clinical trial processes, excellent communication and interpersonal skills, and the ability to travel to clinical sites as needed. A meticulous approach to work and a commitment to maintaining the highest standards of research ethics are essential.
Key Responsibilities:
- Monitor clinical trial sites to ensure compliance with protocols, GCP, and regulatory guidelines.
- Conduct site initiation visits, routine monitoring visits, and close-out visits.
- Verify the accuracy, completeness, and integrity of clinical trial data.
- Ensure proper documentation and maintenance of site regulatory files.
- Train and support investigators and site staff on study procedures and requirements.
- Identify and resolve site-level issues and escalate as necessary.
- Liaise with study participants, investigators, and other stakeholders.
- Oversee drug accountability at trial sites.
- Contribute to the development of study protocols and case report forms.
- Ensure timely data entry and query resolution.
- Bachelor's degree in Life Sciences, Nursing, Pharmacy, or a related healthcare field.
- Minimum of 3 years of experience as a Clinical Research Associate.
- In-depth knowledge of Good Clinical Practice (GCP) guidelines and regulatory requirements.
- Experience in site monitoring and management.
- Strong understanding of clinical trial processes and documentation.
- Excellent written and verbal communication skills.
- Proficiency in clinical trial management software and electronic data capture (EDC) systems.
- Ability to travel to clinical sites as required.
- Strong organizational skills and attention to detail.
- Ability to work independently and as part of a team.
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0
Senior Clinical Research Scientist - Drug Development
88201 Al Seef
BHD130000 Annually
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Posted 5 days ago
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Job Description
Our client is actively seeking a highly accomplished Senior Clinical Research Scientist to join their cutting-edge pharmaceutical research division. This is a fully remote position, offering the flexibility to work from anywhere while contributing to critical drug development initiatives. You will be responsible for designing, planning, and executing clinical trials, from Phase I through Phase IV, ensuring adherence to regulatory requirements and scientific rigor. This role demands a deep understanding of pharmaceutical sciences, clinical trial methodologies, and regulatory guidelines (e.g., FDA, EMA). You will collaborate closely with internal teams, including R&D, regulatory affairs, and medical affairs, as well as external investigators, CROs, and key opinion leaders. The successful candidate will play a vital role in analyzing clinical data, interpreting results, and contributing to regulatory submissions.
Key Responsibilities:
Qualifications:
This is an outstanding opportunity for a dedicated scientist to make a significant contribution to bringing life-saving therapies to patients globally, all within a flexible, remote work setting.
Key Responsibilities:
- Develop clinical trial protocols and study designs that align with strategic objectives.
- Oversee the operational execution of clinical trials, ensuring quality and compliance.
- Manage relationships with Contract Research Organizations (CROs) and other vendors.
- Analyze and interpret clinical trial data, preparing study reports and summaries.
- Contribute to the development of regulatory submission documents (e.g., IND, NDA, MAA).
- Provide scientific and clinical expertise to cross-functional teams.
- Stay current with scientific literature, emerging technologies, and regulatory trends in drug development.
- Identify and engage with key opinion leaders (KOLs) in relevant therapeutic areas.
- Ensure ethical conduct of clinical research and patient safety throughout study duration.
- Participate in the evaluation of new drug candidates and therapeutic strategies.
Qualifications:
- Ph.D. or M.D. in a relevant life science discipline (e.g., Pharmacology, Medicine, Biology).
- Minimum of 7 years of experience in clinical research and drug development within the pharmaceutical or biotechnology industry.
- Extensive experience in designing, managing, and reporting on Phase I-IV clinical trials.
- In-depth knowledge of ICH-GCP guidelines and regulatory submission processes.
- Proven ability to analyze complex clinical data and translate findings into actionable insights.
- Excellent scientific writing and communication skills, with experience in preparing publications and regulatory documents.
- Strong project management and organizational abilities.
- Demonstrated success in leading cross-functional teams in a remote environment.
- Ability to work independently, manage multiple priorities, and meet tight deadlines.
- Experience in therapeutic areas such as oncology, immunology, or cardiovascular disease is highly desirable.
This is an outstanding opportunity for a dedicated scientist to make a significant contribution to bringing life-saving therapies to patients globally, all within a flexible, remote work setting.
This advertiser has chosen not to accept applicants from your region.
1
Senior Formulation Scientist - Drug Development
75331 Southern, Southern
BHD105000 Annually
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Posted 5 days ago
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Job Description
Our client, a leading pharmaceutical company operating from **Nuwaidrat, Southern, BH**, is seeking an accomplished Senior Formulation Scientist to join their innovative Research and Development team. This vital role focuses on the design, development, and optimization of novel drug delivery systems and pharmaceutical formulations. The ideal candidate will possess a profound understanding of pharmaceutics, drug stability, excipient compatibility, and dosage form design for various routes of administration. You will play a key part in advancing drug candidates from pre-clinical stages through to clinical development, ensuring efficacy, safety, and manufacturability.
Key Responsibilities:
Key Responsibilities:
- Design and execute experiments for the development of oral, injectable, topical, or other dosage forms.
- Investigate and select appropriate excipients and active pharmaceutical ingredients (APIs) for formulation development.
- Develop and optimize formulations to achieve desired drug release profiles, stability, and bioavailability.
- Conduct pre-formulation studies, including solid-state characterization and solubility enhancement techniques.
- Perform compatibility studies between APIs and excipients.
- Develop and validate analytical methods for the characterization of drug products and intermediates.
- Troubleshoot formulation-related issues encountered during development and scale-up.
- Collaborate closely with analytical development, process chemistry, and regulatory affairs teams.
- Prepare comprehensive technical reports, documentation for regulatory submissions (IND, NDA), and patent applications.
- Stay abreast of the latest scientific literature, industry trends, and regulatory guidelines in pharmaceutics.
- Mentor junior scientists and contribute to the scientific growth of the R&D department.
- Manage external collaborations with contract research organizations (CROs) as needed.
- Ph.D. or Master's degree in Pharmaceutical Sciences, Pharmaceutics, Chemistry, or a closely related field.
- Minimum of 7 years of hands-on experience in pharmaceutical formulation development, preferably with experience across multiple dosage forms.
- Strong understanding of physical chemistry, materials science, and drug delivery principles.
- Proficiency in laboratory techniques used for formulation development and characterization (e.g., particle size analysis, DSC, TGA, XRPD).
- Experience with common pharmaceutical manufacturing equipment (e.g., blenders, granulators, tablet presses, capsule fillers).
- Familiarity with regulatory requirements for drug development (e.g., FDA, EMA guidelines).
- Excellent problem-solving, critical thinking, and analytical skills.
- Strong written and verbal communication skills, with the ability to present complex scientific information clearly.
- Ability to work independently and collaboratively in a team environment.
- This role requires a hybrid work arrangement, with significant on-site laboratory work in **Nuwaidrat, Southern, BH**.
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2
Senior Clinical Research Scientist - Oncology Drug Development
800 Northern, Northern
BHD140000 Annually
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Posted 5 days ago
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Job Description
Our client is a leading pharmaceutical innovator seeking a Senior Clinical Research Scientist to drive forward critical oncology drug development programs. This is a fully remote position, offering the flexibility to contribute your expertise to life-saving research from your chosen location. The ideal candidate will possess extensive experience in clinical trial design, execution, and data analysis within the oncology therapeutic area. You will play a pivotal role in developing clinical strategies, designing protocols, selecting investigational sites, and ensuring the integrity and compliance of clinical studies. Responsibilities include scientific evaluation of study results, preparation of regulatory submissions, and collaboration with internal and external stakeholders, including regulatory agencies, key opinion leaders (KOLs), and research institutions. This role demands a deep understanding of cancer biology, drug development processes, and current regulatory guidelines. You will be responsible for interpreting complex clinical data, identifying potential risks and opportunities, and making data-driven recommendations to guide project progression. The successful applicant will have a strong publication record and demonstrated leadership in clinical research. We are looking for a highly motivated, results-oriented individual with exceptional analytical and problem-solving skills. The ability to communicate complex scientific and clinical information effectively to diverse audiences is essential. This is an opportunity to make a profound impact on patient lives by contributing to the development of novel cancer therapies. You will be part of a dedicated and passionate team committed to advancing medical science.
Key Responsibilities:
Key Responsibilities:
- Develop and execute clinical development strategies for oncology assets.
- Design and author clinical trial protocols and study documents.
- Provide scientific and clinical leadership throughout the study lifecycle.
- Oversee clinical trial conduct, data monitoring, and safety surveillance.
- Analyze and interpret clinical trial data, prepare study reports.
- Collaborate with cross-functional teams (regulatory, medical affairs, R&D).
- Engage with external experts, investigators, and regulatory authorities.
- Contribute to the preparation of regulatory submissions (e.g., IND, NDA).
- Stay current with scientific advancements and competitive landscape in oncology.
- Mentor junior clinical research scientists and team members.
- M.D. or Ph.D. in a relevant biomedical science (e.g., Oncology, Pharmacology, Biology).
- Minimum of 8 years of experience in clinical research and drug development, with a focus on oncology.
- Proven experience in designing and managing Phase I-III clinical trials.
- Strong understanding of cancer biology, therapeutic targets, and treatment modalities.
- Familiarity with ICH-GCP guidelines and regulatory requirements (FDA, EMA).
- Excellent scientific writing and presentation skills.
- Demonstrated ability to analyze and interpret complex clinical data.
- Strong leadership, interpersonal, and negotiation skills.
- Ability to work independently and effectively in a remote, global team environment.
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3
Principal Scientist - Drug Discovery & Development
67890 Southern, Southern
BHD160000 Annually
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Posted 5 days ago
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Job Description
Our client, a pioneering pharmaceutical company at the forefront of medical innovation, is seeking a highly accomplished Principal Scientist to join their esteemed research and development team. This is a critical, fully remote position, empowering you to leverage your expertise in drug discovery and development from your preferred location. You will be responsible for leading cutting-edge research initiatives, driving the identification and validation of novel therapeutic targets, and advancing promising drug candidates through the preclinical development pipeline. Your role will involve designing and executing complex experiments, interpreting intricate data sets, and generating high-quality scientific reports. Collaboration with cross-functional teams, including medicinal chemists, biologists, toxicologists, and clinical development experts, will be essential. You will contribute significantly to the strategic direction of research programs, evaluating new technologies and methodologies to enhance our drug discovery capabilities. The ideal candidate will possess a deep understanding of molecular biology, pharmacology, and relevant disease areas, with a proven track record of successfully bringing drug candidates from discovery to early development. This position requires exceptional leadership skills, the ability to mentor junior scientists, and a passion for scientific rigor. You will present research findings at scientific conferences and contribute to publications in peer-reviewed journals. As a remote-first organization, we foster a vibrant and collaborative scientific community, providing access to advanced digital tools and platforms that facilitate seamless research collaboration and knowledge sharing across geographical boundaries. We are committed to fostering an environment where groundbreaking discoveries can flourish, enabling us to address unmet medical needs globally.
Key Responsibilities:
Qualifications:
Key Responsibilities:
- Lead and manage multiple drug discovery projects from inception to preclinical development.
- Design, execute, and interpret complex experiments to identify and validate novel therapeutic targets.
- Develop and optimize in vitro and in vivo models for disease research.
- Analyze and report complex biological data, ensuring scientific accuracy and integrity.
- Collaborate with internal and external stakeholders to advance drug candidates.
- Provide scientific leadership and mentorship to research scientists.
- Contribute to the strategic planning and execution of R&D programs.
- Prepare scientific manuscripts, patents, and regulatory documents.
- Stay current with the latest scientific literature and technological advancements in the field.
Qualifications:
- Ph.D. in Molecular Biology, Pharmacology, Biochemistry, or a related life science discipline.
- 10+ years of post-doctoral research experience in the pharmaceutical or biotechnology industry.
- Demonstrated success in leading drug discovery projects and advancing candidates to preclinical stages.
- Expertise in relevant therapeutic areas and disease mechanisms.
- Strong publication record in reputable scientific journals.
- Excellent experimental design and data analysis skills.
- Proven leadership and team management abilities.
- Exceptional written and verbal communication skills.
- Ability to thrive in a remote, collaborative research environment.
This advertiser has chosen not to accept applicants from your region.
4
Remote Senior Formulation Scientist, Drug Development
23456 Saar, Northern
BHD130000 Annually
WhatJobs
Posted 5 days ago
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Job Description
Our client is a dynamic and rapidly growing pharmaceutical company committed to developing innovative therapies for unmet medical needs. We are seeking a highly experienced and dedicated Senior Formulation Scientist to join our remote research and development team. This position offers the unique opportunity to contribute to the entire drug development lifecycle, from preclinical formulation design to supporting clinical trial material manufacturing, all within a flexible, work-from-home setting. You will be responsible for designing, optimizing, and characterizing novel drug delivery systems and formulations for various therapeutic areas. This involves a deep understanding of physicochemical properties of active pharmaceutical ingredients (APIs), excipient selection, and formulation technologies. The ideal candidate will have extensive experience with various dosage forms, including oral solids, injectables, and topical preparations. You will plan and execute laboratory experiments, analyze data, and generate comprehensive reports to support regulatory submissions. Collaboration with analytical chemistry, process development, and regulatory affairs teams will be a significant part of your role. You will also be involved in troubleshooting formulation challenges and identifying creative solutions to optimize drug product performance and stability. Staying current with scientific literature, industry best practices, and regulatory guidelines is crucial. The ability to mentor junior scientists and contribute to the strategic direction of the formulation development group is highly valued. This is an excellent opportunity for a motivated scientist to leverage their expertise in formulation science within a supportive, remote-first environment, contributing to the development of life-changing medicines.
Key Responsibilities:
Key Responsibilities:
- Design, develop, and optimize novel drug formulations for various therapeutic indications.
- Evaluate physicochemical properties of APIs and select appropriate excipients and formulation strategies.
- Conduct laboratory experiments to prepare and characterize different dosage forms (e.g., tablets, capsules, injectables, topicals).
- Perform stability studies and develop analytical methods for formulation assessment.
- Troubleshoot formulation issues and propose scientifically sound solutions.
- Collaborate with analytical, process development, and regulatory affairs teams to advance drug candidates.
- Prepare detailed technical reports, development protocols, and documentation for regulatory submissions.
- Stay updated on the latest advances in drug delivery technologies and pharmaceutical sciences.
- Mentor and provide technical guidance to junior scientists and research associates.
- Contribute to the strategic planning and decision-making for formulation development projects.
- Ph.D. or Master's degree in Pharmaceutical Sciences, Chemistry, Chemical Engineering, or a related field.
- Minimum of 6 years of progressive experience in pharmaceutical formulation development.
- Proven expertise in the design and development of various dosage forms.
- Strong understanding of drug solubility, stability, bioavailability, and drug delivery principles.
- Experience with analytical techniques used in formulation characterization (e.g., HPLC, dissolution testing, DSC, XRPD).
- Excellent experimental design and data analysis skills.
- Strong written and verbal communication skills, with experience in report writing and technical documentation.
- Ability to work independently and effectively manage multiple projects in a remote setting.
- Familiarity with regulatory guidelines (e.g., FDA, EMA) pertaining to drug product development.
This advertiser has chosen not to accept applicants from your region.
5
Lead Pharmaceutical Scientist, Drug Discovery & Development
21002 Seef, Capital
BHD130000 Annually
WhatJobs
Posted 5 days ago
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Job Description
Our client, a renowned pharmaceutical company committed to advancing healthcare, is seeking a highly skilled and innovative Lead Pharmaceutical Scientist to join their dynamic R&D team in Seef, Capital, BH . This critical role will focus on the preclinical stages of drug discovery and development, driving the identification, optimization, and characterization of novel therapeutic candidates. The Lead Pharmaceutical Scientist will lead a team of experienced researchers, guiding them in experimental design, data analysis, and the interpretation of results for complex biological assays and compound screening. You will be responsible for designing and executing research strategies, collaborating with medicinal chemists, pharmacologists, and toxicologists to advance drug candidates through the pipeline. A deep understanding of molecular biology, biochemistry, and pharmacology, coupled with hands-on experience in *in vitro* and *in vivo* model systems, is essential. Expertise in specific therapeutic areas such as oncology, immunology, or neuroscience is highly desirable. The ideal candidate will possess strong project management skills, the ability to manage multiple projects concurrently, and a proven track record of contributing to successful drug development programs. Excellent communication and presentation skills are required to effectively disseminate research findings to internal stakeholders and potential partners. This role offers a significant opportunity to contribute to the development of life-changing medicines and shape the future of pharmaceutical innovation.
Key Responsibilities:
Key Responsibilities:
- Lead and mentor a team of scientists in drug discovery and preclinical development.
- Design, develop, and validate biological assays for drug screening and characterization.
- Oversee *in vitro* and *in vivo* studies to evaluate drug efficacy and safety.
- Analyze and interpret complex experimental data, drawing meaningful conclusions.
- Collaborate with cross-functional teams including medicinal chemistry, pharmacology, and toxicology.
- Contribute to the strategic planning and execution of drug discovery programs.
- Prepare research reports, technical documentation, and regulatory submissions.
- Present research findings at internal meetings and external scientific conferences.
- Stay current with scientific literature and advancements in relevant therapeutic areas.
- Ensure adherence to laboratory safety protocols and Good Laboratory Practice (GLP) standards.
- Ph.D. in Pharmacology, Biochemistry, Molecular Biology, or a related life science discipline.
- Minimum of 8 years of relevant postdoctoral or industry experience in drug discovery.
- Proven experience in leading research teams and managing R&D projects.
- Expertise in a specific therapeutic area (e.g., oncology, immunology, infectious diseases).
- Hands-on experience with a variety of *in vitro* and *in vivo* preclinical models.
- Strong understanding of drug development processes from discovery to early clinical stages.
- Proficiency in data analysis software and statistical methods.
- Excellent communication, presentation, and interpersonal skills.
- Ability to work effectively in a collaborative, team-oriented environment.
- Experience with assay development and validation is required.
This advertiser has chosen not to accept applicants from your region.
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6
Principal Scientist - Drug Discovery and Development
101 Riffa, Southern
BHD150000 Annually
WhatJobs
Posted 5 days ago
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Job Description
Our client, a leading pharmaceutical research company, is seeking a highly accomplished Principal Scientist to drive innovation in drug discovery and development. This critical, lab-based role will be situated in our state-of-the-art facilities in **Riffa, Southern, BH**. You will lead research efforts, design and execute complex experiments, and contribute significantly to the advancement of novel therapeutic candidates. The ideal candidate will possess a deep scientific understanding of molecular biology, pharmacology, or a related discipline, coupled with a proven track record of success in preclinical drug development. You will mentor junior scientists, collaborate with cross-functional teams, and play a key role in shaping the company's research pipeline. This position offers the chance to work on cutting-edge projects that have the potential to transform patient care.
Responsibilities:
Qualifications:
Responsibilities:
- Lead independent research projects from target identification through to preclinical candidate selection.
- Design, execute, and interpret complex biological and pharmacological experiments.
- Develop and validate new assays and experimental models for drug discovery.
- Analyze and present complex data sets, drawing meaningful conclusions and recommending next steps.
- Mentor and guide junior scientists, fostering their scientific and professional development.
- Collaborate effectively with medicinal chemistry, DMPK, and toxicology teams.
- Contribute to the development of research strategies and project proposals.
- Stay current with scientific literature and emerging trends in the pharmaceutical industry.
- Prepare scientific manuscripts for publication and present findings at international conferences.
- Ensure adherence to laboratory safety protocols and best practices.
- Contribute to intellectual property generation and patent filings.
- Manage project timelines and resources effectively to meet research objectives.
Qualifications:
- Ph.D. in Molecular Biology, Pharmacology, Biochemistry, or a related life science discipline.
- Minimum of 10 years of postdoctoral and/or industry experience in drug discovery.
- Extensive experience in designing and conducting in vitro and in vivo pharmacology studies.
- Proven track record of successfully advancing drug candidates through the discovery pipeline.
- Expertise in relevant therapeutic areas is highly desirable.
- Strong understanding of drug development processes from discovery to early clinical stages.
- Excellent leadership, mentoring, and team collaboration skills.
- Exceptional analytical, problem-solving, and critical-thinking abilities.
- Outstanding written and verbal communication skills.
- Proficiency in data analysis software and scientific reporting.
- Experience with cell-based assays, high-throughput screening, and molecular biology techniques.
- Ability to work independently and manage multiple research projects concurrently.
This advertiser has chosen not to accept applicants from your region.
7
Chemical Engineer - Research & Development
10005 Jbeil
BHD85000 Annually
WhatJobs
Posted 5 days ago
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Job Description
Our client has an exciting opportunity for a dedicated Chemical Engineer to join their dynamic Research & Development team in Janabiyah, Northern, BH . This role is focused on pioneering new chemical processes and product formulations, contributing to the company's future innovations. The successful candidate will be responsible for conducting laboratory-scale experiments, analyzing results, and developing scalable processes for potential commercialization. Key duties include literature reviews, feasibility studies, process optimization, and the preparation of detailed technical reports. You will collaborate closely with chemists, materials scientists, and other engineers to advance research projects from benchtop to pilot scale. Proficiency in laboratory techniques, analytical instrumentation, and statistical analysis is required. Experience with process simulation software is a plus. This is a hands-on, laboratory-intensive position requiring full-time presence at our client's R&D facility in Janabiyah, Northern, BH . A Bachelor's or Master's degree in Chemical Engineering or a closely related field is essential. Candidates with prior research experience or a strong academic background in relevant areas are encouraged to apply. We are looking for an inquisitive, detail-oriented individual with strong problem-solving skills and a passion for scientific discovery. Excellent communication and teamwork abilities are crucial for success in this collaborative research environment. Join our client and be at the forefront of chemical innovation in Janabiyah, Northern, BH , contributing to the development of next-generation products and technologies.
This advertiser has chosen not to accept applicants from your region.
8
Remote Pharmaceutical Research & Development Manager
5003 Busaiteen, Muharraq
BHD110000 Annually
WhatJobs
Posted 3 days ago
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Job Description
Our client is seeking a highly experienced and visionary Remote Pharmaceutical Research & Development Manager to lead critical initiatives in drug discovery and development. This is a fully remote position, offering the flexibility to work from anywhere while driving innovation in the pharmaceutical sector. The ideal candidate will possess a deep understanding of drug development processes, regulatory affairs, and scientific research methodologies.
Responsibilities include overseeing the entire R&D pipeline, from early-stage research and preclinical studies to clinical trial support and regulatory submission preparation. You will be responsible for managing cross-functional teams of scientists, chemists, biologists, and project managers, ensuring projects are completed on time, within budget, and to the highest scientific standards. This role involves setting research objectives, developing strategic R&D plans, and identifying new therapeutic targets and innovative drug candidates.
The Pharmaceutical R&D Manager will play a crucial role in fostering a culture of scientific excellence, collaboration, and innovation within the remote team. You will be expected to stay abreast of the latest scientific advancements, emerging technologies, and regulatory changes impacting the pharmaceutical industry. Strong analytical, problem-solving, and decision-making skills are essential. Excellent communication and leadership abilities are required to effectively manage and motivate a distributed team. Our client is committed to advancing healthcare and is looking for a leader who can make a significant contribution to bringing life-changing medicines to patients.
Qualifications include a Ph.D. in Pharmacy, Pharmaceutical Sciences, Chemistry, Biology, or a related field. A minimum of 10 years of progressive experience in pharmaceutical R&D, with at least 5 years in a management or leadership role, is required. Proven success in drug discovery, development, and navigating regulatory pathways (e.g., FDA, EMA) is essential. Experience managing remote R&D teams and complex project portfolios is highly desirable. Strong understanding of GMP, GLP, and GCP regulations is a must. Excellent strategic planning, organizational, and interpersonal skills are critical for this role. The ability to effectively communicate complex scientific and strategic information to diverse stakeholders, including senior executives, is paramount.
Responsibilities include overseeing the entire R&D pipeline, from early-stage research and preclinical studies to clinical trial support and regulatory submission preparation. You will be responsible for managing cross-functional teams of scientists, chemists, biologists, and project managers, ensuring projects are completed on time, within budget, and to the highest scientific standards. This role involves setting research objectives, developing strategic R&D plans, and identifying new therapeutic targets and innovative drug candidates.
The Pharmaceutical R&D Manager will play a crucial role in fostering a culture of scientific excellence, collaboration, and innovation within the remote team. You will be expected to stay abreast of the latest scientific advancements, emerging technologies, and regulatory changes impacting the pharmaceutical industry. Strong analytical, problem-solving, and decision-making skills are essential. Excellent communication and leadership abilities are required to effectively manage and motivate a distributed team. Our client is committed to advancing healthcare and is looking for a leader who can make a significant contribution to bringing life-changing medicines to patients.
Qualifications include a Ph.D. in Pharmacy, Pharmaceutical Sciences, Chemistry, Biology, or a related field. A minimum of 10 years of progressive experience in pharmaceutical R&D, with at least 5 years in a management or leadership role, is required. Proven success in drug discovery, development, and navigating regulatory pathways (e.g., FDA, EMA) is essential. Experience managing remote R&D teams and complex project portfolios is highly desirable. Strong understanding of GMP, GLP, and GCP regulations is a must. Excellent strategic planning, organizational, and interpersonal skills are critical for this role. The ability to effectively communicate complex scientific and strategic information to diverse stakeholders, including senior executives, is paramount.
This advertiser has chosen not to accept applicants from your region.
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