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
- ...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
...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$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- ...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
- ...Associate Regulatory Affairs Director, US Lead, Regulatory Science & Execution The Associate Regulatory Affairs Director, US Lead, Regulatory Science... ...colleagues within Alexion (i.e., commercial, research, clinical development, medical affairs, business development,...Hourly payTemporary workWork at officeFlexible hours3 days per week
$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$157.5k - $262.5k
...The Director of Regulatory Affairs will be responsible for assigned projects... ...ex-US regulatory activities associated with the project teams. Develop... ...for the development and writing of regulatory submission... ...Overseeing regulatory review of clinical trial labelling and CMC...Full timeWork at officeLocal areaWorldwideNight 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... ...Advanced 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
- 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
- ...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
- ...Senior Group Director, Clinical Scientist At AstraZeneca, we pride ourselves on crafting a... ...Operates in compliance with GCP and relevant regulatory guidelines. Essential Requirements:... ...exposure to protocol development and writing. Scientific writing: Experience...Immediate start3 days per week
- ...Associate Restaurant Manager Reports to: Restaurant General Manager Directly Supervises: AGMs / Shift Managers / Team Members The... ...ARM assumes full responsibility for specific financial controls, crew training assignments and the screening of prospective employees...GangsShift work
- 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...
$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$20.13 - $30.25 per hour
...including: oil changes, basic inspections, repairing tires Reading, writing, and math skills. Preferred Qualifications ~2 years of... ...external qualifications or training certifications. Our Crew Knows Benefits ~ Medical, Dental and Vision – Starting day...GangsDaily paidTemporary workLocal areaFlexible hours$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- ...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
$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$151.23k - $198.49k
...potential of digital health, transforming how clinical research is conducted, how care is... .... About the Opportunity: As an Associate Director Scientist within Evinova Quantitative... ...reports, presentations, publications, and regulatory materials Integrate AI-enabled analytics...Temporary workWork at officeWorldwide3 days per week$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
- ...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...
$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...- 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
Do you want to receive more vacancies?
Subscribe and receive similar vacancies to Associate Director, Clinical Regulatory Writing (CReW). Be the first to apply!
- associate director Gaithersburg, MD
- associate director clinical research Gaithersburg, MD
- associate manager Gaithersburg, MD
- associate director clinical data management Gaithersburg, MD
- associate scientific director Gaithersburg, MD
- senior director clinical development Gaithersburg, MD
- director of health and wellness Gaithersburg, MD
- medical and health service manager Gaithersburg, MD
- director clinical pharmacology Gaithersburg, MD
- clinical director Gaithersburg, MD



