Associate Director, Clinical Regulatory Writing (CReW)
$136.78k - $205.18kAstraZeneca
AstraZeneca is seeking an Associate Director, R&I Clinical Regulatory Writing in Gaithersburg, MD. This position requires a strategic leader to manage clinical regulatory writing activities, author clinical documents, and ensure high-quality submissions. The ideal candidate holds a Bachelor's degree with at least 5 years in the medical writing field, demonstrating excellent communication skills and a strong understanding of regulatory processes. The role offers a competitive salary ranging from $136,784.80 to $205,177.20 USD, along with various benefits including health insurance and a retirement plan. #J-18808-Ljbffr AstraZeneca
- ...Are you passionate about Regulatory Writing? Would you like to have an impact on... ...fitness center, employee healthcare clinic, electric vehicle charging... ...We are now recruiting an Associate Director, Clinical Regulatory Writing (CReW). The Clinical Regulatory Writing...GangsHourly payTemporary work
- Are you passionate about Regulatory Writing? Would you like to have an impact on... ...fitness center, employee healthcare clinic, electric vehicle charging... ...teams. We are now recruiting an Associate Director, Clinical Regulatory Writing (CReW). The Clinical Regulatory Writing...GangsHourly payFull timeTemporary workWork at office
- ...The Clinical Regulatory Writing team provides expert communications leadership to drug projects and authors strategically important clinical... ...and approvals. The Clinical Regulatory Writing Associate Director is expected to: Independently manage clinical regulatory...Suggested
$133.04k - $199.56k
AstraZeneca GmbH in Gaithersburg, MD, is hiring a Clinical Regulatory Writer, Associate Director/Manager. This hybrid role requires a BS in Life Sciences and at least 7 years of medical writing experience in the pharmaceutical industry. You'll manage writing activities,...Suggested3 days per week$133.04k - $199.56k
Job Title: Clinical Regulatory Writer, Associate Director / Manager Location: Gaithesrburg, MD- Hybrid (3 days onsite) Introduction to role: Are you ready... ...? As an Associate Director in Clinical Regulatory Writing, you'll play a pivotal role in translating life-changing...SuggestedHourly payTemporary workWork at officeFlexible hours3 days per week- ...Associate Director/Senior Manager, Regulatory Affairs Based in Germantown, Maryland Precigen is seeking a highly... ...'s quality, CMC, preclinical, and clinical drug development programs,... .... Specifically assisting with the writing and/or editing of scientific sections...Work at office
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$136.5k - $227.5k
...Vacancy Name Associate Director, TMF Operations and Clinical Operations Analytics Vacancy No VN520 Employment Type Full Time Location... ...line with relevant regulations (e.g., ICH-GCP, and regulatory requirements such as EMA and MHRA) and industry best...Full timeContract work$137k - $235.75k
...best talent for the role of Associate Director, Oncology Epidemiology .... ...and study conduct across the clinical development program. May... ...with the FDA and other Regulatory Agencies regarding regulatory... ...methods. Experience with writing observational study...Full timeTemporary workLocal areaRemote work$145k - $175k
...Kolon TissueGene, Inc. Kolon TissueGene, Inc. (KTG) is a clinical-stage biopharmaceutical company pioneering cell and gene... ...improve the quality of life for patients worldwide. As Associate Director, Regulatory Affairs , you will play a central role in shaping the regulatory...Full timeWork at officeLocal areaImmediate startWorldwideMonday to FridayFlexible hoursAfternoon shift$118.07k - $177.11k
...Audit readiness support for regulatory inspections queries related... ...knowledge of CFRs, EuDRA and associated guidances, regulations and annexes... ...of CGT products for clinical use in humans. Desired Requirements... ...Degree. Experience writing and reviewing SOPs and other...Hourly payContract workTemporary work- EmergencyMD in Gaithersburg, MD is looking for an Associate Director, R&D Finance. This critical role involves leading finance for MASH Phase... .... Candidates should have over five years of experience in clinical R&D finance within a public biopharma setting, along with a...
$249.83k - $374.74k
...Respiratory Translational Sciences and Clinical Development (TSCD) team, we... ...Do Asa Medical Director, you will provide medical and... ...study design as well writing protocols, key study and health... ...groups. ~ Medical Lead for regulatory communication and preparation...Temporary workWork at officeFlexible hours3 days per week- ...NASDAQ: ALT) is a late clinical-stage... ...metabolic dysfunction-associated steatohepatitis (MASH)... ...Description The Senior Director, Clinical Quality Assurance... ...compliance with ICH‑GCP, regulatory expectations, industry... ...documentation practices (GDP). Write standard operating...For contractorsLocal area
- ...of the time and expect the same from your crew. In addition: staffing, paperwork,... ...telephone orders. Take inventory and complete associated paperwork. Clean equipment and... ...make correct monetary change. Verbal, writing, and telephone skills to take and process...GangsShift work
- The Associate Director, Product Management leads a product team (typically 2-3) responsible for a specific product or set of products. This... ...experience in product and/or experience management Strong writing ability Strong business acumen Experience with Agile software...Work experience placementLocal area
- The Senior Group Director, Clinical Scientist will lead a group of clinical scientists within Hematology... ...in compliance with GCP and relevant regulatory guidelines. Essential Requirements... ...exposure to protocol development and writing. Scientific writing: Experience...
- ...analysis and value and scientific evidence generation to support clinical, economic, and patient-centered value propositions and... ...knowledge of epidemiology, economics, psychometrics, and medical writing.- **Project Management:** Proven ability to manage complex projects...For contractors
- ...currently seeking a Medical Director . Medical Director will participate... ...in all aspects of in-house clinical programs and trials. The role... ...• Demonstrated good medical writing skills Professional... ..., including knowledge of regulatory requirements in clinical development...
$150k - $190k
...visionary and operationally astute Associate Director of Artificial Intelligence,... ...science and life-saving clinical research. Sitting at... ...Proposal Authorship: Personally write key sections of technical... ...valued at $15M+. ~ Regulatory Experience: Proven track record...Local areaImmediate startFlexible hours- ...Associate Director, Cell Therapy Trade Compliance Operations Introduction to role: Are you ready to build a world-class trade compliance... ...chain of identity and chain of custody while meeting strict regulatory expectations. Your leadership will ensure patient materials,...Hourly payTemporary workWork at officeImmediate startFlexible hours3 days per week
$17 - $21 per hour
...540 - BLT Gaithersburg - Gaithersburg, MD 20879 Position Type: Associate Restaurant Manager Salary Range: $17.00 - $21.00 hourly Reports... ...ARM assumes full responsibility for specific financial controls, crew training assignments and the screening of prospective employees...GangsHourly payAll shiftsShift work$20.13 - $30.25 per hour
...changes Basic inspections Repairing tires ~ Reading, writing, and math skills. Preferred Qualifications ~2 years... ...external qualifications or training certifications. Our Crew Knows Benefits ~ Medical, Dental and Vision – Starting day...GangsDaily paidMinimum wagePrice workFull timeTemporary workPart timeLocal areaFlexible hours$151.4k - $236.6k
Description POSITION SUMMARY: This director level position oversees and is responsible for all aspects of clinical development, including clinical research, operations... ...team Participate in designing and writing clinical trial protocols Manage clinical site...Contract workTemporary workWork at officeFlexible hours- ...Global Clinical Development Medical Director Hybrid Working: 3 days per week in the office... ...including Patient Safety, Biometrics, Regulatory Affairs, Clinical Operations, and Translational... ...Adverse Events and review and writing of safety narrative reports ~...Hourly payTemporary workWork at officeFlexible hours3 days per week
$130k
...Description Must Have Technical/Functional Skills End to end clinical data management Vendor management Strong expertise in discrepancy... ...in Database UAT and EUT, as well as a solid background in writing specifications for listings and edit checks. Familiarity with...- ...consultancy firm in Gaithersburg, Maryland is seeking a candidate for clinical data management roles. The ideal candidate will have a Bachelor... .... They should also be comfortable preparing metrics and writing specifications for data management. Competitive compensation with...
- ...CMC Director/Senior Director, Regulatory Affairs Altimmune (NASDAQ: ALT) is a clinical stage biopharmaceutical company focused on developing treatments for obesity and... ...treatment of obesity, metabolic dysfunction-associated steatohepatitis (MASH), alcohol-associated...Local area
- A leading biopharmaceutical company is seeking a Director of Promotional Regulatory Affairs to steer US promotional regulatory strategy. This role involves ensuring compliance and leading innovative regulatory strategy across various channels. The ideal candidate will...
- ...to oversee strategic contributions to product development and regulatory strategy. The candidate will mentor statistical staff, lead complex... ...of relevant experience, and demonstrate leadership skills in clinical trials. Strong communication and project management skills are...Flexible hours
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