166 Scientific Research jobs in Bahrain
Clinical Research Associate
3045 Tubli
BHD65000 Annually
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Our client, a leading pharmaceutical company, is seeking a diligent and experienced Clinical Research Associate (CRA) to join their innovative team. This hybrid role offers a blend of remote flexibility and in-office collaboration. The CRA will be responsible for monitoring and managing clinical trials to ensure they are conducted, recorded, and reported in accordance with the protocol, standard operating procedures (SOPs), and good clinical practice (GCP) guidelines. You will serve as the primary liaison between the research sites and the study sponsor, ensuring the integrity of the data and the safety of the study participants. This involves site initiation, routine monitoring visits, and site closure activities, as well as resolving data discrepancies and ensuring regulatory compliance.
Key Responsibilities:
Qualifications:
Key Responsibilities:
- Conduct site initiation, interim monitoring, and close-out visits in compliance with GCP and regulatory requirements.
- Verify the accuracy, completeness, and consistency of clinical trial data by reviewing source documents and electronic case report forms (eCRFs).
- Ensure adherence to the study protocol, SOPs, and applicable regulations.
- Manage communication with investigators and site staff, providing guidance and support.
- Identify, document, and escalate any deviations, adverse events, or protocol violations.
- Train site staff on study-specific procedures and data collection requirements.
- Prepare visit reports and follow up on action items with study sites.
- Contribute to the development and review of clinical study documentation, including protocols and informed consent forms.
- Ensure all trial-related materials are properly maintained and archived.
- Participate in investigator meetings and internal team meetings.
Qualifications:
- Bachelor's degree in a life science, nursing, or related field.
- Minimum of 3 years of experience as a Clinical Research Associate or in a similar clinical trial management role.
- Thorough understanding of ICH-GCP guidelines and relevant regulatory requirements.
- Experience with electronic data capture (EDC) systems and clinical trial management systems (CTMS).
- Excellent organizational, time management, and problem-solving skills.
- Strong interpersonal and communication skills, both written and verbal.
- Ability to travel to study sites as required (approximately 50% travel expected).
- Detail-oriented with a high level of accuracy.
- Proficiency in Microsoft Office Suite.
- Knowledge of specific therapeutic areas is a plus.
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0
Research Associate Intern
Saturn Consultants
Posted today
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Job Description
We are seeking a Research Associate Intern for our company who will use their understanding of a company’s core operations, competitive advantages, and goals to carry out research on how to structure, run, and grow the business in addition to other administrative tasks.
**Responsibilities**
- Develop an understanding of the existing business (including products/services, customers, competitors, the overall market and trends) through careful research and analysis
- Understand how major stakeholders are thinking about near-term growth, generally and in reference to specific growth initiatives, through interviews with these stakeholders
- Conduct a total addressable market analysis for the business’ core market, assess major industry trends affecting the business, and describe what impact these trends may have on the business
- Review research reports and conduct secondary research to hone in on ideal buyer type and assess customer demand for the company’s existing products and services
- Map out direct and indirect competitors, including potential future competitors, for existing and potential revenue channels
- Define a go-to-market strategy, including testing out potential marketing channels (if applicable)
**Skills and Qualifications**
- Bachelor’s degree in finance, operations, research, statistics, math, economics, or related analytical discipline preferred
- Proficiency with analytical and presentation tools (Excel pivot tables, graphing, PowerPoint)
- A natural curiosity and a “big picture” mentality
- Proficiency conducting market research, including analyzing and synthesizing research reports and conducting primary research
- An understanding of marketing channels and go-to-market strategies
- Excellent spoken and written communication; comfort reaching out to and interviewing the company’s management, employees, and customer base
**Job Types**: Full-time, Internship
Contract length: 6 months
**Salary**: BD100.000 - BD150.000 per month
**Education**:
- Bachelor's (required)
**Responsibilities**
- Develop an understanding of the existing business (including products/services, customers, competitors, the overall market and trends) through careful research and analysis
- Understand how major stakeholders are thinking about near-term growth, generally and in reference to specific growth initiatives, through interviews with these stakeholders
- Conduct a total addressable market analysis for the business’ core market, assess major industry trends affecting the business, and describe what impact these trends may have on the business
- Review research reports and conduct secondary research to hone in on ideal buyer type and assess customer demand for the company’s existing products and services
- Map out direct and indirect competitors, including potential future competitors, for existing and potential revenue channels
- Define a go-to-market strategy, including testing out potential marketing channels (if applicable)
**Skills and Qualifications**
- Bachelor’s degree in finance, operations, research, statistics, math, economics, or related analytical discipline preferred
- Proficiency with analytical and presentation tools (Excel pivot tables, graphing, PowerPoint)
- A natural curiosity and a “big picture” mentality
- Proficiency conducting market research, including analyzing and synthesizing research reports and conducting primary research
- An understanding of marketing channels and go-to-market strategies
- Excellent spoken and written communication; comfort reaching out to and interviewing the company’s management, employees, and customer base
**Job Types**: Full-time, Internship
Contract length: 6 months
**Salary**: BD100.000 - BD150.000 per month
**Education**:
- Bachelor's (required)
This advertiser has chosen not to accept applicants from your region.
1
Research Associate Intern
Saturn Consultants
Posted today
Job Viewed
Job Description
We are seeking a Research Associate Intern for our company who will use their understanding of a company’s core operations, competitive advantages, and goals to carry out research on how to structure, run, and grow the business in addition to other administrative tasks.
**Responsibilities**
- Develop an understanding of the existing business (including products/services, customers, competitors, the overall market and trends) through careful research and analysis
- Understand how major stakeholders are thinking about near-term growth, generally and in reference to specific growth initiatives, through interviews with these stakeholders
- Conduct a total addressable market analysis for the business’ core market, assess major industry trends affecting the business, and describe what impact these trends may have on the business
- Review research reports and conduct secondary research to hone in on ideal buyer type and assess customer demand for the company’s existing products and services
- Map out direct and indirect competitors, including potential future competitors, for existing and potential revenue channels
- Define a go-to-market strategy, including testing out potential marketing channels (if applicable)
**Skills and Qualifications**
- Bachelor’s degree in finance, operations, research, statistics, math, economics, or related analytical discipline preferred
- Proficiency with analytical and presentation tools (Excel pivot tables, graphing, PowerPoint)
- A natural curiosity and a “big picture” mentality
- Proficiency conducting market research, including analyzing and synthesizing research reports and conducting primary research
- An understanding of marketing channels and go-to-market strategies
- Excellent spoken and written communication; comfort reaching out to and interviewing the company’s management, employees, and customer base
**Job Types**: Full-time, Internship
Contract length: 6 months
**Salary**: BD100.000 - BD150.000 per month
**Responsibilities**
- Develop an understanding of the existing business (including products/services, customers, competitors, the overall market and trends) through careful research and analysis
- Understand how major stakeholders are thinking about near-term growth, generally and in reference to specific growth initiatives, through interviews with these stakeholders
- Conduct a total addressable market analysis for the business’ core market, assess major industry trends affecting the business, and describe what impact these trends may have on the business
- Review research reports and conduct secondary research to hone in on ideal buyer type and assess customer demand for the company’s existing products and services
- Map out direct and indirect competitors, including potential future competitors, for existing and potential revenue channels
- Define a go-to-market strategy, including testing out potential marketing channels (if applicable)
**Skills and Qualifications**
- Bachelor’s degree in finance, operations, research, statistics, math, economics, or related analytical discipline preferred
- Proficiency with analytical and presentation tools (Excel pivot tables, graphing, PowerPoint)
- A natural curiosity and a “big picture” mentality
- Proficiency conducting market research, including analyzing and synthesizing research reports and conducting primary research
- An understanding of marketing channels and go-to-market strategies
- Excellent spoken and written communication; comfort reaching out to and interviewing the company’s management, employees, and customer base
**Job Types**: Full-time, Internship
Contract length: 6 months
**Salary**: BD100.000 - BD150.000 per month
This advertiser has chosen not to accept applicants from your region.
2
Senior Clinical Research Associate
BH-808 Busaiteen, Muharraq
BHD85000 Annually
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Job Description
Our client, a global leader in pharmaceutical innovation, is seeking a highly skilled and experienced Senior Clinical Research Associate (CRA) to join their dedicated, fully remote clinical operations team. This role offers a fantastic opportunity to contribute to life-changing research from the comfort of your home office, collaborating with a dynamic and dispersed team of clinical professionals. The Senior CRA will be responsible for monitoring and managing clinical trials, ensuring compliance with study protocols, Good Clinical Practice (GCP) guidelines, and all applicable regulatory requirements. You will play a crucial role in site selection, initiation, monitoring, and close-out activities, ensuring the accuracy, completeness, and timeliness of data collected. The ideal candidate will possess a deep understanding of the drug development process, clinical trial design, and regulatory landscapes. Excellent communication, organizational, and problem-solving skills are essential for effective site management and issue resolution. This remote position requires strong self-discipline, proactive communication, and the ability to travel to clinical sites as needed. You will be expected to build and maintain strong relationships with investigators, site staff, and internal project teams. Responsibilities include performing site visits (remote and/or on-site), reviewing essential documents, monitoring subject safety and data integrity, and ensuring timely resolution of site-specific issues. Your expertise will be vital in ensuring the successful execution of clinical trials and the delivery of high-quality data that supports regulatory submissions and product approvals. This is a challenging yet rewarding role for a motivated CRA looking to make a significant impact on global health.
Key Responsibilities:
Key Responsibilities:
- Conduct remote and on-site monitoring visits to clinical trial sites.
- Ensure compliance with protocols, GCP, and regulatory requirements.
- Perform site selection, initiation, interim monitoring, and close-out visits.
- Verify the accuracy and completeness of clinical data and source documentation.
- Manage site relationships and provide training and support to site staff.
- Identify and resolve site-specific issues and deviations.
- Prepare monitoring reports and track action items.
- Contribute to the development of study-related documents.
- Ensure timely reporting of adverse events.
- Bachelor's degree in Life Sciences, Nursing, Pharmacy, or a related field.
- Minimum of 5 years of experience as a Clinical Research Associate.
- Extensive knowledge of GCP, ICH guidelines, and regulatory requirements.
- Proven experience in monitoring clinical trials across various therapeutic areas.
- Excellent written and verbal communication skills.
- Strong organizational and time management abilities.
- Proficiency in clinical trial management systems (CTMS) and electronic data capture (EDC) systems.
- Ability to travel to clinical sites as required (percentage will vary).
This advertiser has chosen not to accept applicants from your region.
3
Clinical Research Associate - Oncology
0000 Jaww, Southern
BHD60000 Annually
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Job Description
Our client is seeking a diligent and experienced Clinical Research Associate (CRA) with a specialization in Oncology to join their pharmaceutical research team based in **A'ali, Northern, BH**. This crucial role involves monitoring and managing clinical trials, ensuring adherence to protocols, regulatory requirements, and Good Clinical Practice (GCP) guidelines. The CRA will be responsible for site selection, initiation, monitoring, and close-out visits for investigational sites, verifying the accuracy and completeness of clinical data. You will work closely with investigators, site staff, and internal project teams to facilitate the smooth execution of trials, ensuring patient safety and data integrity. Key responsibilities include reviewing source documents, source data verification (SDV), monitoring patient eligibility, and managing study supplies. The ideal candidate will possess strong organizational skills, excellent attention to detail, and the ability to manage multiple priorities in a dynamic environment. Experience with electronic data capture (EDC) systems and clinical trial management systems (CTMS) is essential. A background in oncology research is highly preferred, along with a solid understanding of cancer treatments and clinical trial methodologies in this field. This position offers the opportunity to contribute to life-saving therapies and work within a collaborative and supportive pharmaceutical environment. Our client is dedicated to advancing medical treatments and provides ample opportunities for professional development. The role involves travel to clinical sites as needed, combined with remote administrative tasks.
Key Responsibilities:
Key Responsibilities:
- Conduct site initiation, interim, and close-out monitoring visits.
- Ensure study conduct is in compliance with protocol, SOPs, and GCP guidelines.
- Verify the accuracy, completeness, and consistency of clinical data.
- Manage site communications and provide training to site personnel.
- Oversee patient recruitment and enrollment efforts.
- Monitor drug accountability and investigational product management.
- Prepare and present monitoring visit reports.
- Identify and escalate site issues and risks to the project team.
- Ensure regulatory documentation is complete and maintained.
- Contribute to the development of study protocols and other study documents.
- Bachelor's degree in a life science, nursing, or related field.
- Minimum of 3 years of experience as a Clinical Research Associate.
- Proven experience in oncology clinical trials is highly desirable.
- In-depth knowledge of ICH-GCP guidelines and regulatory requirements.
- Proficiency with EDC and CTMS systems.
- Excellent monitoring and data verification skills.
- Strong interpersonal and communication abilities.
- Ability to work independently and manage time effectively.
- Willingness to travel to clinical sites as required.
- Valid driver's license and passport.
This advertiser has chosen not to accept applicants from your region.
4
Clinical Research Associate (CRA)
40005 Shahrakan
BHD70000 Annually
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Job Description
Our client, a leading pharmaceutical company dedicated to advancing healthcare solutions, is seeking a motivated and detail-oriented Clinical Research Associate (CRA) to join their team in **Manama, Capital, BH**. This hybrid role offers a dynamic mix of on-site responsibilities and remote flexibility, allowing for efficient management of clinical trials. The CRA will play a pivotal role in ensuring the successful execution of clinical research studies, adhering to strict regulatory guidelines and protocols. Key responsibilities include site selection and initiation, monitoring trial progress, ensuring data integrity, and managing patient safety. You will be the primary liaison between the investigational sites and the sponsoring company, building strong relationships with investigators and site staff. The ideal candidate will possess a deep understanding of Good Clinical Practice (GCP) guidelines, regulatory requirements, and clinical trial processes. This role requires meticulous attention to detail, excellent organizational skills, and the ability to travel to clinical trial sites as needed. You will be responsible for reviewing source documents, verifying case report forms (CRFs), and addressing any discrepancies or queries that arise during the trial. Contribution to site training, protocol adherence, and overall trial compliance will be paramount. We are looking for a proactive individual with a passion for clinical research and a commitment to improving patient outcomes through innovative pharmaceutical development. Responsibilities:
- Conduct site visits for monitoring, initiation, and close-out activities.
- Ensure compliance with study protocols, GCP, and regulatory requirements.
- Verify data accuracy and completeness by reviewing source documents and CRFs.
- Manage investigational product and supplies at study sites.
- Address site queries and provide support to investigators and study staff.
- Identify and escalate potential issues and risks to trial management.
- Prepare and present study updates and reports.
- Assist in the preparation of regulatory submission documents.
- Bachelor's degree in Life Sciences, Nursing, Pharmacy, or a related field.
- Proven experience as a Clinical Research Associate or in a similar clinical trial role.
- In-depth knowledge of GCP, ICH guidelines, and regulatory requirements.
- Experience with electronic data capture (EDC) systems.
- Strong monitoring and auditing skills.
- Excellent communication, interpersonal, and organizational skills.
- Ability to travel to sites as required.
This advertiser has chosen not to accept applicants from your region.
5
Clinical Research Associate (Pharmaceutical)
88101 Durrat Al Bahrain
BHD90000 Annually
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Job Description
Our client, a prominent pharmaceutical research organization, is seeking a meticulous and dedicated Clinical Research Associate (CRA) to join their team in Sitra, Capital, BH . This role is integral to the successful execution of clinical trials, ensuring adherence to protocols and regulatory standards. The CRA will be responsible for monitoring clinical trial sites to ensure data accuracy, patient safety, and compliance with Good Clinical Practice (GCP) guidelines and regulatory requirements. Key responsibilities include site selection and initiation visits, routine monitoring visits (on-site and remote), site management and close-out activities, verifying accuracy and completeness of case report forms (CRFs) and source documents, ensuring proper drug accountability, training site staff on study protocols and procedures, resolving site issues and discrepancies, and maintaining effective communication between study sites, the project team, and regulatory authorities. The ideal candidate will possess a Bachelor's degree in a life science, nursing, or related field, with at least 3-5 years of experience as a CRA or in a similar clinical research role. Strong knowledge of ICH-GCP guidelines and regulatory requirements is essential. Excellent organizational, communication, and interpersonal skills are required. Proficiency in clinical trial management systems (CTMS) and electronic data capture (EDC) systems is expected. The ability to travel to assigned clinical sites is a requirement for this position. This is an excellent opportunity to contribute to life-changing medical research and advance your career in clinical operations within a reputable pharmaceutical company. Join us and play a vital role in bringing innovative treatments to patients.
This advertiser has chosen not to accept applicants from your region.
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6
Senior Clinical Research Associate
7004 Riffa, Southern
BHD110000 Annually
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Job Description
Our client, a groundbreaking pharmaceutical company, is seeking a highly experienced Senior Clinical Research Associate to join their fully remote team. This is an exceptional opportunity to contribute to life-changing drug development from the convenience of your home office. You will be responsible for overseeing the conduct of clinical trials at investigative sites, ensuring adherence to protocols, Good Clinical Practice (GCP) guidelines, and regulatory requirements. The Senior Clinical Research Associate will manage site selection, initiation, monitoring, and close-out activities. This includes conducting site visits (remote or in-person as needed, with primary focus on remote monitoring tools), reviewing source documents, ensuring data accuracy and completeness, and resolving data queries. You will serve as the primary point of contact for investigative sites, providing support and guidance to investigators and study staff. Strong communication, organizational, and interpersonal skills are essential for building effective relationships with site personnel and internal project teams. This role requires a deep understanding of clinical trial processes, regulatory landscapes, and therapeutic areas. The successful candidate will be proactive, detail-oriented, and capable of managing multiple studies and sites concurrently in a remote setting. We are looking for a dedicated professional committed to advancing medical research and ensuring patient safety. Responsibilities:
Qualifications:
This fully remote opportunity is ideal for candidates located near Riffa, Southern, BH who are seeking a challenging and rewarding career in pharmaceutical research.
- Manage and monitor assigned clinical trial sites to ensure compliance with protocols, GCP, and regulatory requirements.
- Conduct remote and/or on-site monitoring visits, including site initiation, interim monitoring, and close-out.
- Assess protocol adherence, data integrity, and patient safety at investigative sites.
- Review case report forms (CRFs) and source documents for accuracy and completeness.
- Identify and resolve data discrepancies and queries in collaboration with site staff and data management.
- Ensure timely submission of essential documents and regulatory compliance at the site level.
- Serve as the primary liaison between investigative sites, study teams, and other stakeholders.
- Provide training and support to site personnel on protocol requirements and study procedures.
- Contribute to the development of study-related documents, such as monitoring plans and site manuals.
- Manage site issues and escalations, ensuring prompt resolution.
Qualifications:
- Bachelor's degree in a life science, nursing, or related field.
- Minimum of 5 years of experience as a Clinical Research Associate (CRA) in the pharmaceutical or biotech industry.
- In-depth knowledge of GCP, ICH guidelines, and relevant regulatory requirements.
- Experience in managing multiple clinical trials and sites simultaneously.
- Proficiency in clinical trial management systems (CTMS) and electronic data capture (EDC) systems.
- Excellent monitoring, auditing, and data review skills.
- Strong organizational, time management, and problem-solving abilities.
- Exceptional written and verbal communication skills.
- Demonstrated ability to work effectively in a fully remote environment, maintaining productivity and engagement.
- Relevant certifications (e.g., ACRP, SoCRA) are a plus.
This fully remote opportunity is ideal for candidates located near Riffa, Southern, BH who are seeking a challenging and rewarding career in pharmaceutical research.
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7
Senior Clinical Research Associate (Pharma)
8001 Southern, Southern
BHD75000 Annually
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Our client, a leading pharmaceutical company, is seeking an experienced Senior Clinical Research Associate (CRA) to join their dedicated clinical operations team. This role will involve the oversight and management of clinical trials, ensuring they are conducted, recorded, and reported in accordance with the protocol, standard operating procedures (SOPs), and Good Clinical Practice (GCP) guidelines. Based in **Nuwaidrat, Southern, BH**, this hybrid position offers a blend of on-site responsibilities and remote work flexibility. The Senior CRA will be responsible for site selection, initiation, monitoring, and close-out visits to ensure the quality and integrity of clinical trial data. You will serve as the primary point of contact for investigational sites, addressing any issues that arise and ensuring compliance with study requirements. Key duties include reviewing patient records, verifying data accuracy, and ensuring adherence to ethical and regulatory standards. The ideal candidate will possess strong knowledge of drug development processes, clinical trial methodologies, and regulatory requirements. Excellent communication, negotiation, and interpersonal skills are essential for building strong relationships with site staff and internal stakeholders. You will also play a role in mentoring junior CRAs and contributing to the continuous improvement of clinical trial processes. This position requires a proactive, detail-oriented individual with a proven ability to manage multiple projects and ensure timely completion of trial milestones. Your contributions will be vital in bringing life-saving therapies to patients. Key responsibilities include:
- Conducting site selection, initiation, interim monitoring, and close-out visits in accordance with protocol and GCP.
- Ensuring compliance with all study-related procedures, regulations, and ethical standards.
- Verifying the accuracy, completeness, and consistency of clinical trial data.
- Managing investigational product accountability and drug storage requirements.
- Overseeing informed consent process and patient recruitment/retention strategies.
- Building and maintaining strong relationships with investigators and site staff.
- Resolving site-level issues and escalating problems as necessary.
- Ensuring timely submission of study-related documents and reports.
- Participating in the development and review of clinical trial protocols and case report forms (CRFs).
- Mentoring and providing guidance to junior clinical research associates.
- Bachelor's degree in Life Sciences, Nursing, Pharmacy, or a related field; advanced degree is a plus.
- Minimum of 4-6 years of experience as a Clinical Research Associate in the pharmaceutical industry.
- In-depth knowledge of GCP, ICH guidelines, and regulatory requirements.
- Proven experience in monitoring clinical trials across various therapeutic areas.
- Excellent interpersonal, communication, and negotiation skills.
- Strong organizational and time management abilities with a keen eye for detail.
- Ability to work independently and manage travel requirements effectively.
- Proficiency in clinical trial management software and electronic data capture (EDC) systems.
- Experience mentoring or supervising junior staff is highly desirable.
This advertiser has chosen not to accept applicants from your region.
8
Senior Clinical Research Associate - Pharmaceutical
99999 Tubli
BHD90000 Annually
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Job Description
Our client is a globally recognized pharmaceutical company seeking an experienced Senior Clinical Research Associate (CRA) to join their dynamic clinical operations team in Isa Town, Southern, BH . This role will primarily involve managing and monitoring clinical trials, ensuring compliance with protocols, government regulations, and Good Clinical Practice (GCP) guidelines. You will be responsible for site selection, initiation, monitoring, and closure activities, maintaining close communication with investigators, site staff, and internal project teams. The ideal candidate will possess a strong understanding of clinical trial processes, therapeutic areas, and regulatory requirements within the pharmaceutical industry. Your responsibilities will include reviewing and verifying case report forms (CRFs), managing data discrepancies, and ensuring the accuracy and completeness of clinical data. You will also be tasked with conducting site visits (pre-study, initiation, routine monitoring, and close-out) to assess protocol adherence, patient safety, and data integrity. This position requires exceptional organizational, analytical, and communication skills. You will play a vital role in advancing the company's pipeline of innovative medicines by ensuring the efficient and compliant execution of clinical trials. The ability to work independently, manage multiple sites, and navigate complex research environments is essential. We are looking for a dedicated professional with a commitment to scientific excellence and patient safety, who can contribute significantly to the success of our clinical research programs. This hybrid role offers a blend of on-site responsibilities and remote work flexibility.
Key Responsibilities:
Qualifications:
Key Responsibilities:
- Conduct site selection, initiation, routine monitoring, and close-out visits for clinical trials.
- Ensure compliance with study protocols, GCP guidelines, and regulatory requirements.
- Verify the accuracy, completeness, and consistency of clinical trial data.
- Manage and resolve data discrepancies identified during monitoring activities.
- Serve as the primary point of contact between clinical trial sites and the study team.
- Oversee site performance and identify areas for improvement.
- Train and mentor investigative site staff on study procedures and requirements.
- Prepare and present monitoring reports to management and study teams.
- Ensure timely submission of required study documentation.
- Maintain effective working relationships with investigators, site personnel, and internal stakeholders.
- Contribute to the development of study protocols and monitoring plans.
Qualifications:
- Bachelor's degree in Life Sciences, Nursing, Pharmacy, or a related field.
- Minimum of 5 years of experience as a Clinical Research Associate in the pharmaceutical industry.
- In-depth knowledge of GCP, ICH guidelines, and relevant regulatory requirements.
- Proven experience in monitoring clinical trials across various therapeutic areas.
- Strong understanding of clinical trial processes, from site initiation to close-out.
- Excellent organizational, time management, and problem-solving skills.
- Proficient in electronic data capture (EDC) systems and clinical trial management systems (CTMS).
- Strong written and verbal communication skills.
- Ability to travel to clinical trial sites as required.
- Detail-oriented with a high degree of accuracy.
- Relevant certifications (e.g., ACRP, SoCRA) are a plus.
This advertiser has chosen not to accept applicants from your region.
9