154 Statutory Research jobs in Bahrain
Executive Legal Assistant
1002 Busaiteen, Muharraq
BHD55000 Annually
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Our client, a prestigious law firm, is actively seeking an exceptionally organized and detail-oriented Executive Legal Assistant to provide comprehensive administrative and legal support within their **Busaiteen, Muharraq, BH** office. The successful candidate will be instrumental in ensuring the smooth operation of the legal department, managing complex schedules, and facilitating seamless communication between attorneys, clients, and courts.
Key Responsibilities:
Required Qualifications:
This role offers a competitive compensation package and the opportunity to work in a supportive and professional legal environment.
Key Responsibilities:
- Manage and coordinate executive calendars, including scheduling appointments, meetings, and court appearances with precision.
- Prepare, proofread, and edit legal documents, correspondence, and pleadings, ensuring accuracy and adherence to firm standards.
- Organize and maintain physical and electronic filing systems for case files, ensuring easy accessibility and confidentiality.
- Conduct legal research using various databases and resources to assist attorneys in case preparation.
- Facilitate communication with clients, witnesses, opposing counsel, and court personnel in a professional and courteous manner.
- Arrange travel logistics, including flights, accommodations, and itineraries for attorneys.
- Process expense reports and manage billing and invoicing procedures.
- Handle incoming and outgoing mail and manage document distribution.
- Provide general administrative support, such as answering phones, managing correspondence, and greeting visitors.
- Prepare meeting agendas, take minutes, and distribute them to relevant parties.
- Assist with the onboarding of new legal staff and paralegals.
- Ensure all legal documentation is properly formatted and filed according to court rules and internal procedures.
- Anticipate the needs of the legal team and proactively address potential issues.
- Maintain strict confidentiality of all client information and firm matters.
Required Qualifications:
- High school diploma or equivalent required; Associate's or Bachelor's degree preferred.
- Minimum of 3-5 years of experience as a legal assistant or executive assistant in a legal setting.
- Proficiency in legal terminology and procedures.
- Exceptional organizational and time management skills.
- Advanced proficiency in Microsoft Office Suite (Word, Excel, Outlook, PowerPoint).
- Strong written and verbal communication skills.
- Ability to work independently and as part of a team.
- High level of discretion and ability to handle sensitive information.
- Experience with legal practice management software is a plus.
- Detail-oriented with a commitment to accuracy.
- Must be able to demonstrate a proactive approach to problem-solving.
This role offers a competitive compensation package and the opportunity to work in a supportive and professional legal environment.
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0
Legal & PR Assistant
Manama, Capital
Ramee Hotels and Restaurants Management Co.W.L.L
Posted today
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Male Law graduates who are freshers. Able to draft letter, communicate in Arabic and English fluently. Should be able to handle immigration, LMRA and related matters.
Will be part of the HR team and will be part of all staff related activities too.
**Salary**: BD380.000 per month
Will be part of the HR team and will be part of all staff related activities too.
**Salary**: BD380.000 per month
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1
Clinical Research Associate
1155 Diplomatic Area
BHD60000 Annually
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Our client, a rapidly expanding pharmaceutical company, is seeking a meticulous and experienced Clinical Research Associate (CRA) to join their dedicated team in **Isa Town, Southern, BH**. This critical role involves overseeing clinical trials from initiation to closure, ensuring compliance with protocols, regulatory requirements, and Good Clinical Practice (GCP) guidelines. You will be responsible for site selection, initiation visits, routine monitoring, and close-out visits to ensure the quality and integrity of clinical trial data. This includes verifying data accuracy, reviewing case report forms (CRFs), and managing essential trial documentation. You will serve as the primary liaison between the investigative sites and the sponsor, building strong working relationships and addressing any queries or issues that arise promptly. Monitoring patient safety and ensuring adherence to study protocols are paramount. This position requires a thorough understanding of drug development processes and regulatory landscapes. The ideal candidate will possess a Bachelor's degree in a life science, nursing, or a related field, with a minimum of 3 years of experience as a CRA or in a similar clinical research role. Strong knowledge of ICH-GCP guidelines and other relevant regulatory requirements is essential. Excellent organizational, problem-solving, and communication skills are a must. The ability to manage multiple projects simultaneously, travel to various clinical sites as needed, and maintain accurate and detailed records is required. Experience with electronic data capture (EDC) systems is highly desirable. This is an exciting opportunity to contribute to groundbreaking research and development within the pharmaceutical sector, offering a competitive salary, comprehensive benefits, and significant career advancement potential in **Isa Town, Southern, BH**.
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2
Clinical Research Associate
211 Al Jasra
BHD75000 Annually
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Our client, a prominent pharmaceutical company, is looking for a dedicated and meticulous Clinical Research Associate (CRA) to join their team in Hidd, Muharraq, BH . The CRA will play a vital role in overseeing clinical trials, ensuring compliance with protocols, and maintaining the integrity of data. This position involves site monitoring, data collection, and ensuring adherence to Good Clinical Practice (GCP) guidelines. The successful candidate will be responsible for managing multiple study sites, conducting site initiation visits, interim monitoring, and close-out visits.
Key responsibilities include:
The ideal candidate will hold a Bachelor's degree in a life science, nursing, or a related field, with a minimum of 3 years of experience as a CRA or in a similar role within the pharmaceutical or biotechnology industry. Strong understanding of clinical trial processes, regulatory requirements, and data management is essential. Excellent organizational, communication, and interpersonal skills are a must. The ability to travel to study sites frequently is also required. This is an excellent opportunity for a driven professional to contribute to groundbreaking research in Hidd, Muharraq, BH .
Key responsibilities include:
- Monitor clinical trial sites to ensure compliance with study protocols, FDA regulations, and GCP guidelines.
- Verify the accuracy, completeness, and integrity of clinical data.
- Build and maintain positive relationships with investigators and site staff.
- Conduct source data verification (SDV) and ensure all trial-related documentation is accurate and up-to-date.
- Identify, evaluate, and resolve issues that arise during the clinical trial process.
- Prepare and present monitoring visit reports.
- Participate in the selection and training of new clinical trial sites.
- Ensure timely submission of regulatory documents.
- Contribute to the development of study protocols and other trial-related documents.
The ideal candidate will hold a Bachelor's degree in a life science, nursing, or a related field, with a minimum of 3 years of experience as a CRA or in a similar role within the pharmaceutical or biotechnology industry. Strong understanding of clinical trial processes, regulatory requirements, and data management is essential. Excellent organizational, communication, and interpersonal skills are a must. The ability to travel to study sites frequently is also required. This is an excellent opportunity for a driven professional to contribute to groundbreaking research in Hidd, Muharraq, BH .
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3
Clinical Research Associate
66778 Hamad Town, Northern
BHD90000 Annually
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Posted 1 day ago
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Our client, a globally recognized pharmaceutical company at the forefront of medical innovation, is seeking a dedicated and experienced Clinical Research Associate to contribute to groundbreaking drug development. This critical role, based in **Hamad Town, Northern, BH**, will involve overseeing and managing clinical trials to ensure they are conducted, recorded, and reported in accordance with protocol, standard operating procedures (SOPs), and regulatory requirements. Your responsibilities will include site selection, initiation, monitoring, and close-out visits. You will ensure the quality and integrity of data collected, verify source documentation, and maintain accurate study documentation. Building and maintaining strong relationships with investigators and site staff will be key to your success. You will also be responsible for resolving data discrepancies, ensuring compliance with Good Clinical Practice (GCP) guidelines, and managing study supplies. This position requires a deep understanding of the drug development process and regulatory landscapes, including FDA and EMA regulations. The ideal candidate will possess excellent organizational skills, strong attention to detail, and exceptional communication and interpersonal abilities. A proactive approach to problem-solving and the ability to work independently and as part of a cross-functional team are essential. Proficiency in clinical trial management systems (CTMS) and electronic data capture (EDC) systems is highly desirable. If you are passionate about advancing healthcare and possess the expertise to drive successful clinical trials, we invite you to join our innovative team. Our client offers a collaborative work environment and significant opportunities for career advancement within the pharmaceutical industry.
Key Responsibilities:
Key Responsibilities:
- Perform site selection, initiation, monitoring, and close-out visits for clinical trials.
- Ensure compliance with study protocols, SOPs, and regulatory guidelines (e.g., GCP, ICH).
- Verify accuracy and completeness of clinical trial data and source documentation.
- Build and maintain strong working relationships with clinical investigators and site personnel.
- Identify, document, and resolve site-specific issues and deviations.
- Manage study supplies and ensure proper storage and handling of investigational products.
- Train site staff on study-specific procedures and regulatory requirements.
- Prepare and present study progress reports to the project team and management.
- Ensure timely submission of essential study documents.
- Contribute to the development and review of study protocols and other trial-related documents.
- Bachelor's degree in Life Sciences, Nursing, Pharmacy, or a related field.
- Minimum of 3-5 years of experience as a Clinical Research Associate.
- Thorough understanding of clinical trial processes and regulatory requirements (GCP, ICH).
- Experience with site monitoring and data verification.
- Proficiency in CTMS and EDC systems.
- Excellent communication, organizational, and problem-solving skills.
- Ability to travel as required for site visits.
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4
Clinical Research Associate
78787 Muharraq, Muharraq
BHD90000 Annually
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Posted 1 day ago
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Job Description
Our client is looking for a dedicated and meticulous Clinical Research Associate to contribute to groundbreaking pharmaceutical studies in Muharraq, Muharraq, BH . This vital role involves overseeing and managing clinical trials in compliance with Good Clinical Practice (GCP) guidelines, regulatory requirements, and protocol objectives. The CRA will be responsible for site selection, initiation, monitoring, and close-out visits, ensuring the accuracy and completeness of clinical data. You will serve as the primary liaison between the sponsor and investigational sites, fostering strong working relationships and providing essential support to investigators and study staff. A thorough understanding of drug development processes and medical terminology is crucial for success in this position.
Key Responsibilities:
Qualifications:
Key Responsibilities:
- Conduct pre-study, initiation, interim, and close-out monitoring visits at clinical trial sites.
- Verify the quality and integrity of clinical data through source data verification.
- Ensure compliance with study protocols, regulatory guidelines (e.g., ICH-GCP), and standard operating procedures.
- Train and support site personnel on study-specific procedures and regulatory requirements.
- Manage study documentation and ensure the accurate and timely submission of essential documents.
- Identify and report adverse events and safety information in a timely manner.
- Troubleshoot and resolve issues identified during site visits.
- Prepare monitoring visit reports and follow up on action items.
- Contribute to the development of study-related documents, such as protocols and case report forms (CRFs).
- Maintain effective communication with investigators, site staff, and internal project teams.
Qualifications:
- Bachelor's degree in a life science, nursing, or a related field; advanced degree is a plus.
- Previous experience as a Clinical Research Associate or in a similar role.
- In-depth knowledge of clinical trial methodologies and regulatory affairs.
- Strong understanding of ICH-GCP guidelines and local regulatory requirements.
- Excellent organizational and time management skills.
- Exceptional written and verbal communication skills.
- Proficiency in electronic data capture (EDC) systems and clinical trial management systems (CTMS).
- Ability to travel to investigational sites as required.
- Problem-solving aptitude and attention to detail.
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5
Clinical Research Associate
10200 Askar, Southern
BHD50000 Annually
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Posted 1 day ago
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Our client, a prominent pharmaceutical company, is seeking a dedicated Clinical Research Associate (CRA) to join their innovative team in Tubli, Capital, BH . This role is essential for overseeing clinical trials and ensuring compliance with regulatory standards and protocols. You will be responsible for monitoring study sites, verifying data accuracy, and ensuring the safety and well-being of study participants. The CRA plays a crucial part in the successful execution of clinical research, contributing to the development of new and life-saving medications.
Key responsibilities include site initiation visits, routine monitoring, and close-out visits. You will build strong relationships with investigators and site staff, providing guidance and support throughout the trial. The role requires meticulous attention to detail, excellent organizational skills, and a deep understanding of Good Clinical Practice (GCP) guidelines. You will be expected to manage multiple study sites simultaneously and ensure that all study-related activities are conducted ethically and scientifically. Your ability to identify and resolve issues promptly will be critical to the study's progress.
Qualifications:
Key responsibilities include site initiation visits, routine monitoring, and close-out visits. You will build strong relationships with investigators and site staff, providing guidance and support throughout the trial. The role requires meticulous attention to detail, excellent organizational skills, and a deep understanding of Good Clinical Practice (GCP) guidelines. You will be expected to manage multiple study sites simultaneously and ensure that all study-related activities are conducted ethically and scientifically. Your ability to identify and resolve issues promptly will be critical to the study's progress.
Qualifications:
- Bachelor's degree in Life Sciences, Nursing, Pharmacy, or a related healthcare field.
- Minimum of 2-3 years of experience as a Clinical Research Associate or in a similar clinical research role.
- In-depth knowledge of ICH-GCP guidelines and regulatory requirements.
- Strong understanding of clinical trial processes and documentation.
- Excellent communication, interpersonal, and presentation skills.
- Proficiency in using clinical trial management software.
- Ability to travel as required.
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6
Clinical Research Associate
10501 Diplomatic Area
BHD68000 Annually
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Posted 1 day ago
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Job Description
Our client is seeking a meticulous and dedicated Clinical Research Associate to contribute to their groundbreaking work in the pharmaceutical sector in Isa Town, Southern, BH . This role is crucial for ensuring the successful execution of clinical trials, adhering to stringent regulatory guidelines and protocols. The Clinical Research Associate will be responsible for monitoring trial sites, ensuring data accuracy, and maintaining compliance throughout the research process.
Key Responsibilities:
Qualifications:
Key Responsibilities:
- Conduct site initiation visits, interim monitoring visits, and site closure visits to ensure study protocol adherence and data integrity.
- Verify that study conduct is in compliance with the protocol, FDA regulations, ICH guidelines, and other applicable regulatory requirements.
- Manage and train site staff on study-related procedures and documentation.
- Oversee the informed consent process and ensure patient rights and safety are protected.
- Monitor the accuracy, completeness, and quality of clinical trial data.
- Collect and review essential documents for trial sites.
- Liaise between the study sponsor, investigators, and site staff to ensure effective communication.
- Identify and report any adverse events or protocol deviations promptly.
- Maintain accurate and up-to-date study documentation and records.
- Participate in study team meetings and contribute to problem-solving efforts.
- Ensure all trial-related activities are documented appropriately.
- Contribute to the development of clinical study protocols and other study documents.
Qualifications:
- Bachelor's degree in Life Sciences, Nursing, Pharmacy, or a related field. A Master's degree is a plus.
- Minimum of 3 years of experience as a Clinical Research Associate or in a similar clinical research role.
- In-depth knowledge of Good Clinical Practice (GCP) and regulatory guidelines.
- Experience in monitoring clinical trials across various therapeutic areas.
- Strong understanding of clinical trial processes and documentation requirements.
- Excellent organizational, time management, and problem-solving skills.
- Proficiency in clinical data management systems and Microsoft Office Suite.
- Strong communication and interpersonal skills, with the ability to build rapport with investigators and site staff.
- Detail-oriented with a commitment to accuracy and data quality.
- Ability to travel to clinical trial sites as required.
- Relevant certifications like CRA or CCRA are highly beneficial.
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7
Clinical Research Associate
26001 Riffa, Southern
BHD85000 Annually
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Posted 1 day ago
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Job Description
Our client, a pioneering pharmaceutical company, is seeking a dedicated and experienced Clinical Research Associate (CRA) to join their clinical operations team in **Riffa, Southern, BH**. This critical role involves overseeing and managing clinical trial activities at investigational sites, ensuring compliance with protocols, regulations, and Good Clinical Practice (GCP) guidelines. The ideal candidate will possess a strong scientific background, meticulous attention to detail, and excellent project management skills. You will be responsible for site selection, initiation, monitoring, and close-out, ensuring the quality and integrity of data collected. This position offers a unique opportunity to contribute to the development of life-saving therapies and advance medical science.
Key Responsibilities:
Qualifications:
Key Responsibilities:
- Conduct site visits, including pre-study, initiation, interim monitoring, and close-out visits.
- Verify data accuracy and completeness by reviewing source documents and electronic data capture systems.
- Ensure compliance with study protocols, investigator brochures, and GCP guidelines.
- Monitor patient recruitment and retention efforts at investigational sites.
- Train and support site staff on study requirements and regulatory compliance.
- Manage essential study documents and regulatory binders.
- Identify and report adverse events and protocol deviations.
- Facilitate communication between the sponsor and investigational sites.
- Address site-specific issues and implement corrective actions as needed.
- Prepare monitoring visit reports and track action items.
Qualifications:
- Bachelor's degree in a life science, nursing, or a related field. Advanced degree or relevant certifications are a plus.
- Minimum of 3 years of experience as a Clinical Research Associate or in a similar clinical trial monitoring role.
- In-depth knowledge of GCP, ICH guidelines, and regulatory requirements.
- Experience with various therapeutic areas and study phases.
- Proficiency in clinical trial management software (CTMS) and electronic data capture (EDC) systems.
- Excellent organizational, communication, and interpersonal skills.
- Strong analytical and problem-solving abilities.
- Ability to travel to investigational sites as required.
- Attention to detail and commitment to data integrity.
- Proficiency in English and relevant local languages.
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8
Clinical Research Associate
10101 Riffa, Southern
BHD70000 Annually
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Posted 1 day ago
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Our client is looking for a diligent and proactive Clinical Research Associate to manage and oversee clinical trials in Riffa, Southern, BH . This role is crucial for ensuring the quality, integrity, and compliance of clinical research activities. The Clinical Research Associate will be responsible for site selection, initiation, monitoring, and close-out activities. Key responsibilities include:
- Identifying and qualifying potential clinical trial sites and investigators.
- Conducting site initiation visits to ensure protocol and regulatory compliance.
- Performing routine monitoring visits to assess patient safety, data accuracy, and adherence to the protocol.
- Ensuring all study-related documentation is maintained accurately and in a timely manner.
- Managing study supplies and investigational product at clinical sites.
- Resolving site-specific issues and providing ongoing support to investigators and site staff.
- Preparing monitoring reports and communicating findings to study teams and management.
- Participating in the development of study protocols and case report forms.
- Ensuring compliance with Good Clinical Practice (GCP) guidelines and applicable regulations.
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