78 graphic design artist jobs found

job summary: This is a high level contract role, requiring Direct Global Regulatory Labeling Operations Project Management experience in the Pharma/Biotech industry, as deep knowledge of pharmaceutical labeling regulations, compliance, and processes are critical for this role. The Labeling Project Manager is responsible for all activities associated with the development, creation and execution of labeling for assigned product lines for domestic and/or i

job summary: We are seeking a Manager-level contractor role to support Neuroscience portfolio assets. The contractor will have the opportunity to support launch and on-market assets in Migraine. The purpose of this role is to provide meaningful, hands-on research experience and professional development opportunities to candidates with proven performance and leadership potential. Ideal candidates will combine technical and business knowledge with analytica

job summary: Title: Global Case Management Specialist Location: Remote Reports to: Sr. Manager, PV Operations Global Case Management The Global Case Management Specialist will be responsible for effective execution of the activities of triage, processing, and quality control of individual case safety reports (ICSR) from clinical trials to ensure timely and accurate assessment of adverse event reports. This role will focus on accurate case entry and w

job summary: Sr. Manager, Clinical Supplies (Oral Solid Dose) 6 Month Contract (may extend or convert) Remote (75%) + 1 week / month in South SF Looking for West Coast Based Candidates (travel reimbursed) Must Have: Experience with oral tablet dosage form Phase 1 & Small Biotech experience APAC logistics experience is a plus Strong MS Excel skills Seeking a talented, independent, and highly motivated Senior Manager, Clinical Supplies Planning

job summary: Sr. Pharmacovigilance (PV) Operations Manager | Remote | West Coast This critical role is responsible for managing and overseeing PV operations across clinical development programs, ensuring seamless collaboration with PV vendors. You will play a key role in preparing for the initiation of two global Phase 3 trials, ensuring all PV activities are in place. Your expertise in global trial management, study document review, and vendor oversight

job summary: As the largest staffing and recruitment agency in the world, we can commit to finding you the perfect role that gives you the opportunity to learn and grow in the life sciences arena. Utilizing a recruiter for your job search gives you access to a large network of top employers as well as detailed information about hundreds of positions. Located in 100 countries, our longtime partner is known for being the world's largest producer of vaccines

job summary: Regulatory Affairs Manager II 12 Month Contract | REMOTE Join a leading biopharma company supporting critical regulatory systems initiatives. We're seeking a detail-oriented consultant with expertise in Regulatory Systems, eCTD submission management, and experience working with global IT and cross-functional teams to drive system implementation and Quality Control Process, Documentation & Testing. Key Focus Areas: Regulatory Systems Expertise

job summary: Global Labeling Manager - Regulatory Affairs REMOTE | EST Hours Join a mission-driven team committed to ensuring the safe and effective use of pharmaceutical products worldwide. We're seeking a Global Labeling Manager with a passion for regulatory excellence, precision, and cross-functional collaboration. About the Role: As a Global Labeling Manager, you will drive global labeling strategy and ensure high-quality, compliant labeling documents

Onsite in Bedford, MA 3 days per week. Must have Order Management Systems experience. The Business Analyst for the Commercial Order Management Systems (OMS) plays a pivotal role in bridging the gap between business needs and technology solutions. This role involves gathering, analyzing, and documenting business requirements for the OMS, ensuring the system effectively supports the order management process for radio pharmaceutical products. The Business A

job summary: **Must have a PHD** **Must be familiar with mouse models** **Bilingual in Mandarin/English is Preferred** Randstad Life Sciences is working with a fast-growing biotech company with broad cutting-edge technologies. You will have the best opportunity to learn and utilize the science and business in the fields of immunooncology, animal model gene engineering, preclinical pharmacology, therapeutic antibody discovery, etc. The biggest advantage of

job summary: We are seeking a Regulatory Submission Manager to support global regulatory initiatives and ensure compliance with regulatory requirements for investigational and marketed products. Role involves working closely with cross-functional teams and regulatory leads to support submission activities, labeling development, and strategic regulatory guidance. The ideal candidate has a strong background in regulatory submissions and document review, as

job summary: The MedComm Writer will be accountable for drafting and reviewing scientifically accurate, original content for medical and promotional Pharmaceutical clients. In this role you will work with clients and the Scientific Strategy Lead to plan and develop high-impact, innovative medical communications for assigned brands. You will play a significant role in account growth by building trust with clients through scientific exchange and expertise i

job summary: As the largest staffing and recruitment agency in the world, we can commit to finding you the perfect role that gives you the opportunity to learn and grow in the life sciences arena. Utilizing a recruiter for your job search gives you access to a large network of top employers as well as detailed information about hundreds of positions. Located in 100 countries, our longtime partner is known for being the world's largest producer of vaccines

job summary: The Senior Manager/Associate Director, Medical Communications Ad Promo, represents the Medical function in the Material Review Process to guarantee medical, clinical, and scientific data accuracy, relevance, objectivity, balance and alignment with product label. Functions as the lead medical reviewer and sign-off for all promotional materials in designated area(s) of responsibility. Provides proactive guidance as needed for brand concepts and

job summary: As the largest staffing and recruitment agency in the world, we can commit to finding you the perfect role that gives you the opportunity to learn and grow in the life sciences arena. Utilizing a recruiter for your job search gives you access to a large network of top employers as well as detailed information about hundreds of positions. As the world's leading provider of diagnostic information services, our client is committed to sharing our

job summary: The focus of the clinical laboratory associate will be on the receipt, triage, and accessioning of patient samples submitted to the CLIA laboratory for testing. location: Durham, North Carolina job type: Contract salary: $20 - 22 per hour work hours: 9 to 5 education: Associate responsibilities: Responsible for unpacking samples from shipping containers and accessioning samples into LIMS including troubleshooting sample

job summary: Are you a seasoned biomedical professional passionate about advancing drug delivery to the brain? A leading biopharmaceutical company in North Chicago, IL is seeking a Sr. Principal Research Scientist - Preclinical Project Manager to lead the investigation of innovative device-based drug delivery solutions that improve tissue exposure when systemic delivery is insufficient. This hybrid role involves close collaboration with Discovery and Deve

job summary: Immediate opportunity for a Sr. Regulatory Affairs Associate, CMC to assist the technical team in preparing regulatory filing dossiers, assess changes for regulatory impact, and manage documentation systems. You will participate in Global Regulatory Product Team (GRPT) and Operations Brand Team meetings as needed. As a Senior Associate, RA CMC, you will work with internal and external partners in order to deliver products to patients. Prepare

job summary: The QC Associate I is responsible for supporting key functional, tactical, and operational aspects of the QC Microbiology. Responsibilities include, but are not limited to, training, water and environmental sampling, support for testing. A fundamental understanding of the company's Quality Systems and able to apply it in their daily support functions. Adherence to all GMP requirements, effective interactions/ communication with Quality Contro

job summary: Seeking a skilled Epidemiologist to execute data analyses, contribute to regulatory deliverables, and design epidemiological studies. Proficiency in SAS / R, real-world datasets, and excellent communication skills are essential. We're looking for a motivated professional with an MPH degree and 2+ years of experience, ready to grow in a dynamic pharmaceutical environment. Flexible, Part time hours (20 hours/week) Fully Remote, any time zone in

job summary: A research-driven biopharmaceutical powerhouse focused on developing treatments for complex, hard-to-cure diseases. This esteemed company has brought 32 groundbreaking products to market, including Humira and Lupron, making a significant global impact. If you're ready to make your mark in the field and contribute to the future of innovative therapies, this is the opportunity for you! location: Somerville, New Jersey job type: Contract sa

job summary: As the largest staffing and recruitment agency in the world, we can commit to finding you the perfect role that gives you the opportunity to learn and grow in the life sciences arena. Utilizing a recruiter for your job search gives you access to a large network of top employers as well as detailed information about hundreds of positions. Located in 100 countries, our longtime partner is known for being the world's largest producer of vaccines

job summary: We have a CMC Regulatory Writing Opportunity immediately available. This will be remote, 10 hours per week, and offer a flexible schedule. Hourly Pay. location: Wayne, Pennsylvania job type: Contract salary: $90 - 100 per hour work hours: 9 to 5 education: Masters responsibilities: Work closely with client and internal and partner organization teams to lead development of strategies for organizing and preparing regul

job summary: Sr. Medical Editor - Medical Communications REMOTE / Part-Time 20 hrs/wk | EST Hours ELS Certification Required (Editor in the Life Sciences) via Board of Editors in Life Sciences (BELS) Randstad is hiring a Senior Editor for Scientific Services to join an award-winning, best-in-class in-house agency at a leading pharmaceutical company. This full-service agency develops cutting-edge digital, video, AR/VR, and print assets, consistently outper

job summary: As the world's largest staffing and recruitment agency in the world, we can commit to find you the perfect role that gives you the opportunity to learn and grow in the life sciences arena. Utilizing a recruiter for your job search gives you access to a large network of top employers as well as detailed information about hundreds of positions. With a hefty goal of discovering medical breakthroughs to treat devastating neurological ailments, ou

job summary: As the largest staffing and recruitment agency in the world, we can commit to finding you the perfect role that gives you the opportunity to learn and grow in the life sciences arena. Utilizing a recruiter for your job search gives you access to a large network of top employers as well as detailed information about hundreds of positions. Located in 100 countries, our longtime partner is known for being the world's largest producer of vaccines

job summary: As the largest staffing and recruitment agency in the world, we can commit to finding you the perfect role that gives you the opportunity to learn and grow in the life sciences arena. Utilizing a recruiter for your job search gives you access to a large network of top employers as well as detailed information about hundreds of positions. Our dedicated teams are at the forefront of pioneering beauty tech innovations, meeting individual needs a

job summary: Seeking a talented and motivated individual with expertise in enzymology and biochemical assay development to support small molecule drug discovery. The successful candidate should possess strong technical expertise & exceptional hands-on laboratory skills, have excellent written and oral communication skills, enjoy working in a fast-paced multi-functional team environment, and keep current with field of expertise, including literature and te

job summary: Under general supervision, this position will perform routine sampling and testing in a GMP Manufacturing facility in support of the Microbiology and Environmental Monitoring group. location: Apex, North Carolina job type: Contract salary: $30.00 - 33.56 per hour work hours: 9 to 5 education: Bachelors responsibilities: Assist with environmental monitoring performance qualificationsExecute routine sample collection for envi

job summary: This Laboratory Operations role in Temecula, CA, is ideal for a life science professional with a bachelor's degree or 3-5 years of relevant experience. You'll be crucial in manufacturing products, performing diverse lab operations, and ensuring compliance with cGMP and regulatory standards. The position requires strong aseptic technique, experience with lab equipment, and proficiency in data entry and reporting. You will contribute to process