Explore research and development jobs in What Jobs are available for Research And Development in Atlanta?
Showing 257 Research And Development jobs in Atlanta
Director of Skincare Research & Development
30301 Atlanta, Georgia
$200000 Annually
WhatJobs
Posted 27 days ago
Job Viewed
Job Description
Our client is a prestigious and rapidly expanding entity within the beauty and wellness industry, renowned for its commitment to innovation, efficacy, and luxury. We are seeking an visionary Director of Skincare Research & Development to lead our state-of-the-art R&D division. This senior leadership role is based in our cutting-edge facilities and is responsible for spearheading the discovery, development, and launch of groundbreaking skincare products. You will be instrumental in driving our product pipeline, from initial concept and formulation to clinical testing and regulatory compliance, ensuring our products meet the highest standards of quality and consumer satisfaction. The ideal candidate possesses a profound scientific understanding of dermatological science, ingredient efficacy, and cosmetic formulation, coupled with exceptional leadership and strategic planning capabilities.
Key Responsibilities:
Key Responsibilities:
- Lead and manage the entire skincare product development lifecycle, from ideation to market launch.
- Oversee a team of scientists, formulators, and lab technicians, fostering a culture of innovation and collaboration.
- Develop and execute the strategic R&D roadmap for skincare, identifying market trends and consumer needs.
- Conduct in-depth research into novel ingredients, technologies, and formulation techniques.
- Collaborate with Marketing, Sales, and Operations teams to ensure product concepts align with brand strategy and market demands.
- Manage product efficacy testing, stability studies, and clinical trials, ensuring safety and compliance.
- Maintain strong relationships with raw material suppliers, contract manufacturers, and third-party testing labs.
- Ensure all product development activities comply with relevant regulatory standards (e.g., FDA, international regulations).
- Prepare and present research findings, project updates, and budget proposals to senior management.
- Stay abreast of the latest scientific advancements, competitive landscape, and consumer trends in the skincare industry.
- Advanced degree (Ph.D. or Master's) in Chemistry, Cosmetic Science, Pharmacy, Biology, or a related scientific field.
- Minimum of 10-15 years of progressive experience in skincare R&D, with at least 5 years in a leadership or management role.
- Demonstrated success in bringing multiple innovative skincare products to market.
- Extensive knowledge of cosmetic ingredients, formulation science, and product testing methodologies.
- Strong understanding of dermatological principles and skin physiology.
- Experience with global regulatory requirements for cosmetics.
- Proven ability to lead, mentor, and inspire a scientific team.
- Exceptional strategic thinking, project management, and analytical skills.
- Excellent communication, presentation, and interpersonal skills.
- Proficiency in scientific literature review and data analysis.
Is this job a match or a miss?
Apply Now
0
Clinical Research Associate
30303 Atlanta, Georgia
$90000 Annually
WhatJobs
Posted 21 days ago
Job Viewed
Job Description
Our client, a distinguished pharmaceutical company, is seeking a highly qualified Clinical Research Associate (CRA) to join their dedicated clinical operations team in **Atlanta, Georgia, US**. This critical role involves overseeing and managing clinical trials, ensuring adherence to protocols, regulatory guidelines, and Good Clinical Practice (GCP). The CRA is instrumental in monitoring study sites, verifying data accuracy, and ensuring the safety and well-being of study participants. The ideal candidate will possess a strong scientific background, meticulous attention to detail, and excellent organizational and communication skills. Responsibilities will encompass:
The successful applicant will hold a Bachelor's degree in a life science, nursing, or a related field; a Master's degree or advanced certification is a plus. A minimum of 3-5 years of experience as a Clinical Research Associate is required, with a proven track record of successfully managing clinical trials. Thorough knowledge of ICH-GCP guidelines, FDA regulations, and clinical trial conduct is essential. Excellent communication, interpersonal, and problem-solving skills are paramount. The ability to travel to clinical sites as needed is a requirement for this role, which is based in **Atlanta, Georgia, US**. Our client offers a stimulating work environment, competitive compensation, and opportunities for professional growth within the pharmaceutical industry. We are looking for a proactive, dedicated professional committed to advancing medical research and ensuring the highest standards of clinical trial management.
Key Qualifications:
This is a prime opportunity to contribute to impactful pharmaceutical research and development.
- Monitoring clinical trial sites to ensure compliance with protocols and regulations.
- Verifying the accuracy, completeness, and integrity of clinical data.
- Conducting site initiation, interim monitoring, and close-out visits.
- Ensuring proper training of study site personnel on trial procedures.
- Resolving data discrepancies and query management.
- Reviewing essential documents and study records.
- Reporting on site performance and identifying potential risks.
- Maintaining effective communication with investigators, site staff, and internal project teams.
- Ensuring adherence to safety reporting requirements.
The successful applicant will hold a Bachelor's degree in a life science, nursing, or a related field; a Master's degree or advanced certification is a plus. A minimum of 3-5 years of experience as a Clinical Research Associate is required, with a proven track record of successfully managing clinical trials. Thorough knowledge of ICH-GCP guidelines, FDA regulations, and clinical trial conduct is essential. Excellent communication, interpersonal, and problem-solving skills are paramount. The ability to travel to clinical sites as needed is a requirement for this role, which is based in **Atlanta, Georgia, US**. Our client offers a stimulating work environment, competitive compensation, and opportunities for professional growth within the pharmaceutical industry. We are looking for a proactive, dedicated professional committed to advancing medical research and ensuring the highest standards of clinical trial management.
Key Qualifications:
- Bachelor's degree in Life Sciences, Nursing, or related field (Master's preferred).
- 3-5+ years of experience as a Clinical Research Associate.
- Strong knowledge of ICH-GCP and regulatory guidelines.
- Excellent monitoring and data management skills.
- Superior communication and interpersonal abilities.
- Ability to travel to clinical sites.
This is a prime opportunity to contribute to impactful pharmaceutical research and development.
Is this job a match or a miss?
Apply Now
1
Clinical Research Associate (CRA)
30301 Atlanta, Georgia
$85000 Annually
WhatJobs Direct
Posted today
Job Viewed
Job Description
Our client is searching for a meticulous and dedicated Clinical Research Associate (CRA) to join their expanding pharmaceutical division in Atlanta, Georgia, US . This role is crucial for ensuring the successful execution of clinical trials, adhering to strict regulatory guidelines and ethical standards. The ideal candidate will have a strong background in clinical research, with a deep understanding of Good Clinical Practice (GCP) and relevant regulatory requirements. Responsibilities include site selection and initiation visits, routine monitoring of clinical trial conduct at investigator sites, ensuring data accuracy and integrity, managing study documentation, and acting as a liaison between the sponsor, investigators, and study staff. You will also be responsible for identifying and resolving site-level issues, ensuring patient safety, and verifying compliance with protocols. A Bachelor's degree in a life science, nursing, or a related field is required, along with at least 3 years of experience as a CRA. Excellent organizational, communication, and interpersonal skills are essential, as is the ability to travel frequently to investigator sites. Proficiency in clinical trial management systems and electronic data capture (EDC) systems is highly desirable. This position offers a blend of remote work flexibility and on-site requirements for essential site visits, contributing to groundbreaking medical research. Join our team and play a vital role in bringing innovative pharmaceutical products to patients. We offer a competitive compensation package and opportunities for professional growth within a leading healthcare organization.
Is this job a match or a miss?
Apply Now
2
Senior Clinical Research Associate
30303 Atlanta, Georgia
$90000 Annually
WhatJobs
Posted 17 days ago
Job Viewed
Job Description
Our client, a leader in pharmaceutical innovation, is seeking a highly experienced Senior Clinical Research Associate (CRA) to join their fully remote global clinical operations team. This critical role is instrumental in ensuring the successful execution of clinical trials, adhering to strict regulatory guidelines and quality standards. You will be responsible for monitoring clinical trial sites, ensuring accurate data collection, protocol compliance, and patient safety. The ideal candidate will have a deep understanding of Good Clinical Practice (GCP), regulatory requirements (FDA, EMA), and clinical trial processes. Responsibilities include site initiation visits, routine monitoring, and close-out visits, as well as training and supporting investigators and study staff. You will conduct source data verification, review case report forms (CRFs), and ensure the integrity of trial data. Effective communication and collaboration with internal teams, including project managers, data managers, and medical monitors, as well as external stakeholders, such as investigators and site personnel, are paramount. The ability to manage multiple clinical trial sites remotely, troubleshoot issues proactively, and maintain meticulous documentation is essential. Strong organizational skills, attention to detail, and the ability to work independently with minimal supervision in a remote setting are required. Our client is committed to advancing healthcare through groundbreaking research and offers a supportive environment for professional growth. If you are a dedicated and experienced CRA passionate about bringing life-changing medicines to patients, we encourage you to apply. This position offers the flexibility of remote work combined with the opportunity to contribute to significant advancements in the pharmaceutical industry.
Is this job a match or a miss?
Apply Now
3
Clinical Research Associate - Oncology
30303 Atlanta, Georgia
$95000 Annually
WhatJobs
Posted 19 days ago
Job Viewed
Job Description
Our client, a leading pharmaceutical company dedicated to advancing cancer treatments, is seeking a talented Clinical Research Associate (CRA) to join their innovative team in **Atlanta, Georgia**. This hybrid role offers the chance to contribute to groundbreaking research while enjoying a flexible work arrangement. The CRA will play a critical role in ensuring the successful execution of clinical trials, from site initiation to study close-out.
Responsibilities:
Responsibilities:
- Identify, evaluate, and select clinical trial sites.
- Initiate, monitor, and close-out study sites according to protocol, GCP, and regulatory requirements.
- Ensure the quality, integrity, and accuracy of clinical trial data.
- Train and support study site staff on protocol procedures, regulatory requirements, and data collection.
- Conduct site visits (pre-study, initiation, routine monitoring, and close-out) as needed.
- Manage investigational product supply and accountability at study sites.
- Prepare and present study progress reports to internal stakeholders and investigators.
- Resolve data discrepancies and ensure timely query resolution.
- Maintain accurate and up-to-date site files and documentation.
- Ensure compliance with all applicable regulatory guidelines and company policies.
- Bachelor's degree in a life science, nursing, or related field; advanced degree preferred.
- Minimum of 3-5 years of experience as a Clinical Research Associate in the pharmaceutical or biotech industry.
- Strong knowledge of ICH-GCP guidelines and regulatory requirements.
- Experience in oncology clinical trials is highly desirable.
- Excellent organizational, communication, and interpersonal skills.
- Ability to travel to study sites as required (approximately 30-50% travel).
- Proficiency in clinical trial management systems (CTMS) and electronic data capture (EDC) systems.
- Strong problem-solving skills and attention to detail.
- Ability to work independently and as part of a team.
- Valid driver's license and passport.
Is this job a match or a miss?
Apply Now
4
Senior Clinical Research Associate
30303 Atlanta, Georgia
$110000 Annually
WhatJobs
Posted 20 days ago
Job Viewed
Job Description
Our client, a leading pharmaceutical innovator, is seeking an experienced Senior Clinical Research Associate (CRA) to join their dedicated team. This position offers a hybrid work arrangement, combining remote flexibility with essential in-office collaboration in **Atlanta, Georgia, US**. You will play a crucial role in managing and monitoring clinical trials, ensuring compliance with protocols, regulatory requirements, and ethical standards. The ideal candidate possesses a deep understanding of clinical trial phases, site management, data integrity, and pharmacovigilance. You will be responsible for ensuring the successful execution of clinical studies, from site initiation to study close-out.
Key Responsibilities:
Key Responsibilities:
- Perform site selection, initiation, monitoring, and close-out visits to ensure adherence to study protocols, GCP, and regulatory guidelines.
- Develop and maintain strong relationships with clinical sites, investigators, and site staff.
- Monitor study conduct, data accuracy, and completeness through source data verification (SDV) and review of case report forms (CRFs).
- Ensure timely resolution of data queries and discrepancies.
- Manage investigational product accountability and ensure proper drug handling and storage at sites.
- Oversee patient recruitment and retention efforts at clinical sites.
- Identify, assess, and report adverse events (AEs) and serious adverse events (SAEs) in accordance with company and regulatory requirements.
- Prepare and present study updates and findings to internal teams and site personnel.
- Contribute to the development and review of study-related documents, including protocols, informed consent forms, and study manuals.
- Ensure compliance with all applicable local and international regulations, including FDA regulations and ICH-GCP guidelines.
- Act as a primary point of contact for assigned clinical sites.
- Mentor and provide guidance to junior CRAs as needed.
- Participate in audits and inspections as required.
- Bachelor's degree in a life science, nursing, or related field; advanced degree preferred.
- Minimum of 5 years of experience as a Clinical Research Associate in the pharmaceutical or biotechnology industry.
- Extensive knowledge of clinical trial methodologies, ICH-GCP guidelines, and regulatory requirements.
- Proven experience in managing multiple clinical trial sites simultaneously.
- Strong understanding of medical terminology and clinical trial documentation.
- Excellent communication, interpersonal, and organizational skills.
- Proficiency in using clinical trial management systems (CTMS) and electronic data capture (EDC) systems.
- Ability to travel to clinical sites as needed (approximately 50-70%).
- Demonstrated ability to work independently and as part of a team in a hybrid work environment.
- Strong problem-solving and critical thinking abilities.
Is this job a match or a miss?
Apply Now
5
Senior Clinical Research Associate
30303 Atlanta, Georgia
$95000 Annually
WhatJobs
Posted 20 days ago
Job Viewed
Job Description
Our client, a leading biopharmaceutical innovator, is seeking a highly motivated and experienced Senior Clinical Research Associate (CRA) to join their dynamic team in Atlanta, Georgia, US . This role plays a critical part in the successful execution of clinical trials, ensuring adherence to protocols and regulatory standards. The Senior CRA will be responsible for site selection, initiation, monitoring, and closure activities, as well as managing relationships with investigators and site staff. You will conduct on-site and remote monitoring visits to verify data accuracy, patient safety, and regulatory compliance. This includes reviewing source documents, Case Report Forms (CRFs), and other essential trial documents. The ideal candidate will possess a strong understanding of Good Clinical Practice (GCP) guidelines, FDA regulations, and ICH guidelines. Key responsibilities include ensuring timely data collection, query resolution, and preparation of monitoring visit reports. You will also be involved in training and mentoring junior CRAs and contributing to the development of study-related documents and processes. Excellent communication and interpersonal skills are essential for collaborating effectively with cross-functional teams, including data management, biostatistics, and medical affairs. The ability to manage multiple priorities and meet strict deadlines in a fast-paced environment is crucial. This is an excellent opportunity for a seasoned CRA to make a significant impact on the development of novel therapeutics and advance their career within a reputable organization. The position offers a competitive salary, comprehensive benefits package, and opportunities for professional growth. If you are passionate about bringing life-changing medicines to patients and meet the below qualifications, we encourage you to apply.
Is this job a match or a miss?
Apply Now
Be The First To Know
About the latest Research and development Jobs in Atlanta !
6
Senior Clinical Research Associate
30303 Atlanta, Georgia
$95000 Annually
WhatJobs
Posted 20 days ago
Job Viewed
Job Description
Our client, a leading innovator in pharmaceutical development, is seeking a highly skilled and experienced Senior Clinical Research Associate (CRA) to join their dynamic team in Atlanta, Georgia, US . This role is crucial for overseeing and managing clinical trials, ensuring adherence to protocols, regulations, and ethical standards. The Senior CRA will be responsible for site selection, initiation, monitoring, and closure activities, acting as the primary point of contact between the research site and the sponsor. This position offers a hybrid work model, blending essential in-office collaboration with the flexibility of remote work. You will play a vital role in advancing groundbreaking therapies from conception to market.
Key Responsibilities:
Key Responsibilities:
- Conduct site visits (pre-study, initiation, routine monitoring, close-out) to assess protocol compliance, patient safety, and data integrity.
- Identify, evaluate, and qualify potential clinical trial sites and investigators.
- Provide training and ongoing support to site staff on study procedures, regulatory requirements, and data collection.
- Oversee data collection, query resolution, and ensure timely submission of study documents.
- Ensure compliance with Good Clinical Practice (GCP) guidelines, FDA regulations, and other applicable regulatory requirements.
- Prepare and submit monitoring visit reports and follow-up actions in a timely manner.
- Collaborate with cross-functional teams, including medical monitors, data managers, and project managers, to ensure efficient trial conduct.
- Contribute to the development of study protocols, case report forms (CRFs), and other essential study documents.
- Manage multiple clinical trials simultaneously, ensuring all study milestones are met within projected timelines.
- Proactively identify and address potential risks and issues that may impact study progress or data quality.
- Bachelor's degree in life sciences, nursing, or a related field. Advanced degree (Master's or PhD) preferred.
- Minimum of 5-7 years of experience as a Clinical Research Associate, with a proven track record in managing multi-center clinical trials.
- In-depth knowledge of ICH-GCP guidelines, FDA regulations, and other relevant regulatory frameworks.
- Strong understanding of clinical trial processes, study design, and data management.
- Excellent communication, interpersonal, and negotiation skills.
- Ability to work independently, manage priorities, and meet deadlines in a fast-paced environment.
- Proficiency in clinical trial management software (CTMS) and electronic data capture (EDC) systems.
- Willingness to travel up to 50% to various research sites.
Is this job a match or a miss?
Apply Now
7
Senior Clinical Research Associate (CRA)
30301 Atlanta, Georgia
$100000 Annually
WhatJobs Direct
Posted 1 day ago
Job Viewed
Job Description
Our client, a leading pharmaceutical company, is seeking an accomplished Senior Clinical Research Associate (CRA) to play a vital role in advancing groundbreaking medical research in Atlanta, Georgia . This position is integral to the successful execution of clinical trials, ensuring adherence to study protocols, regulatory requirements, and Good Clinical Practice (GCP) guidelines. The Senior CRA will be responsible for site selection, initiation, monitoring, and close-out activities across multiple investigational sites. This involves conducting regular on-site and remote monitoring visits to verify the accuracy and completeness of source data, review regulatory documents, and ensure the safety and well-being of study participants. You will serve as the primary liaison between the sponsor and the clinical sites, fostering strong working relationships and providing essential support to investigators and study coordinators. The role requires meticulous attention to detail in managing study supplies, investigational product accountability, and data management. You will also be involved in identifying and resolving site-level issues, implementing corrective and preventative actions (CAPAs), and reporting study progress and potential risks to the clinical trial manager. This position demands a comprehensive understanding of drug development processes, clinical trial design, and regulatory affairs within the pharmaceutical industry. The ideal candidate will possess exceptional organizational and communication skills, the ability to work independently, and a proven track record of successful site management. Experience in therapeutic areas such as oncology, cardiology, or neurology is highly desirable. This is an excellent opportunity for a motivated professional to contribute to the development of new therapies and make a significant impact on patient health.
Responsibilities:
Responsibilities:
- Plan, execute, and manage clinical monitoring activities for assigned investigational sites.
- Conduct site initiation visits, routine monitoring visits, and close-out visits according to protocol and SOPs.
- Ensure compliance with study protocols, GCP, FDA regulations, and other applicable guidelines.
- Verify accuracy and completeness of source documentation and clinical data through source data verification (SDV).
- Review and ensure completeness of regulatory binders and essential documents.
- Serve as the primary point of contact between the sponsor and clinical investigators/site staff.
- Train site personnel on study-specific procedures and protocols.
- Identify, document, and resolve site-level issues and implement CAPAs.
- Monitor patient recruitment and retention, and facilitate timely enrollment.
- Manage study supplies and investigational product accountability at sites.
- Prepare and submit monitoring visit reports in a timely manner.
- Contribute to protocol development and study design discussions.
- Identify potential risks and implement mitigation strategies.
- Maintain up-to-date knowledge of therapeutic areas and industry best practices.
- Bachelor's degree in life sciences, nursing, or a related field; advanced degree preferred.
- Minimum of 5 years of experience as a Clinical Research Associate (CRA).
- In-depth knowledge of GCP, ICH guidelines, and regulatory requirements.
- Proven experience in site management, monitoring, and data verification.
- Strong understanding of clinical trial processes and drug development.
- Excellent communication, interpersonal, and organizational skills.
- Ability to work independently and manage multiple priorities effectively.
- Proficiency in clinical trial management systems (CTMS) and electronic data capture (EDC) systems.
- Experience in oncology, cardiology, or other relevant therapeutic areas is a plus.
- Willingness to travel to clinical sites as required.
Is this job a match or a miss?
Apply Now
8
Senior Clinical Research Associate (Remote)
30301 Atlanta, Georgia
$90000 Annually
WhatJobs
Posted 6 days ago
Job Viewed
Job Description
Our client, a cutting-edge biotechnology firm, is seeking an experienced Senior Clinical Research Associate (CRA) to join their fully remote clinical operations team. This position offers the unique opportunity to contribute to groundbreaking clinical trials from the convenience of your home office, serving research sites across the nation. You will be responsible for monitoring clinical trial sites to ensure adherence to protocols, good clinical practices (GCP), and regulatory requirements. This involves conducting remote site visits, performing data verification, ensuring accurate and timely reporting, and maintaining effective communication with investigators, site staff, and internal study teams. Key responsibilities include: developing and implementing site monitoring plans; performing remote source data verification (SDV); ensuring the accuracy, completeness, and integrity of clinical trial data; identifying and resolving site issues; ensuring compliance with safety reporting requirements; and participating in site initiation, interim, and close-out visits (conducted remotely or on-site as necessary, though the role is predominantly remote-focused). The ideal candidate will possess a strong understanding of clinical trial processes, regulatory guidelines (FDA, ICH-GCP), and drug development. Proven experience as a CRA with a track record of successful site management in a remote or hybrid setting is essential. Excellent communication, organizational, and problem-solving skills are required. You must be highly self-motivated, detail-oriented, and capable of working independently with minimal supervision. Proficiency with clinical trial management systems (CTMS), electronic data capture (EDC) systems, and other relevant software is crucial. A Bachelor's degree in a life science, nursing, or a related scientific field is required; advanced degrees are a plus. A minimum of 3-5 years of direct CRA experience is expected. This is a fantastic opportunity for a seasoned CRA looking to leverage their expertise in a dynamic, remote-first environment, contributing to the development of life-saving therapies. If you are passionate about clinical research and thrive in an autonomous, results-driven setting, we encourage you to apply. Our client offers a collaborative virtual work environment and significant opportunities for professional growth. Your dedication will directly impact the success of critical clinical research projects.
Is this job a match or a miss?
Apply Now
9