Jobs / United States / Astrazeneca Pharmaceuticals Lp

Astrazeneca Pharmaceuticals Lp

Global Clinical Development Medical Director

US - Gaithersburg - MD Posted today $249,827

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Skills this job asks for

LeadershipCommunicationEnglish

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Sponsorship verdict

Sponsorship possible

One solid signal, not two. Worth applying, and worth asking about sponsorship early.

  • Employer is on a government sponsor recordThe US Department of Labor certified 99 H-1B/E-3 labor condition applications for this employer between Oct 2025 and Jun 2026 (latest Jun 2026) — the step every H-1B hire needs first.
  • The posting doesn’t mention sponsorshipSilence isn’t a refusal — ask the recruiter before investing much time.
  • No salary bar for this routeH-1B has no fixed salary bar: the employer must pay at least the prevailing wage for the role and area.
  • What Astrazeneca Pharmaceuticals Lp paid sponsored hires in similar roles1 certified filing for “Global Development Medical Director” (Medical Scientists, Except Epidemiologists) in NY: $331k–$331k, median $331k.
  • Confirmed live todayWhen a source last listed this job as open.
Details and sources
Employer is on a government sponsor record
The US Department of Labor certified 99 H-1B/E-3 labor condition applications for this employer between Oct 2025 and Jun 2026 (latest Jun 2026) — the step every H-1B hire needs first. Source: LCA disclosure data (US Department of Labor (OFLC)).
No salary bar for this route
H-1B has no fixed salary bar: the employer must pay at least the prevailing wage for the role and area. Cap-subject employers enter a lottery weighted by wage level. Source: https://www.federalregister.gov/documents/2025/12/29/2025-23853/weighted-selection-process-for-registrants-and-petitioners-seeking-to-file-cap-subject-h-1b, rules effective 2026-02-27.
What Astrazeneca Pharmaceuticals Lp paid sponsored hires in similar roles
1 certified filing for “Global Development Medical Director” (Medical Scientists, Except Epidemiologists) in NY: $331k–$331k, median $331k. Most were filed at wage level II (100%) — 2 lottery entries, ≈31% projected selection odds for cap-subject employers. Source: US Department of Labor LCA disclosure data (Oct 2025 – Jun 2026).

US H-1B: cap-subject employers enter a lottery weighted by wage level — Level I gets 1 entry, Level IV gets 4 (DHS projected selection odds ≈15% at Level I to ≈61% at Level IV). Universities and non-profit research employers are cap-exempt. The $100,000 fee for new petitions from abroad is currently blocked by a court order (appeal pending).

A verdict summarises public evidence. It is not legal advice and never a guarantee: the employer and the immigration authority decide. Sign in to factor in where you can already work.

About the role

Global Clinical Development Medical Director Are you a clinical research physician ready for new opportunities? Would you like to play a pivotal role in the development of potential medicines? If you are passionate about being a medical leader for a cross-functional team in a group that drives action towards the improvement of global public health– join us! As a Global Clinical Development Medical Director you will have a unique opportunity to further elevate the Infectious Disease unit in one of the world’s most respected biopharmaceutical companies. The role holds a great development opportunity for the successful candidate whilst contributing to the positive journey that AstraZeneca is on. Accountabilities : • Providing medical and scientific leadership in the global development of new medicines targeted at indications in the field of infectious diseases • Help design, execute, and interpret clinical trials in one or more development programs (Phase 1 through Phase 3) • Build strong relationships with a network of external scientific specialists and opinion leaders as well as site investigators • Work closely with colleagues in other internal functions including Patient Safety, Biometrics, Regulatory Affairs, Clinical Operations, and Translational Medicine • Medical oversight to ensure the safety of study participants including review of Adverse Events of Special Interest and Serious Adverse Events and review and writing of safety narrative reports • Medical oversight responsibilities for medical activities outsourced to third party vendors • Provide expert medical input and writing of regulatory documents and interactions/responses with regulatory authorities • Provide expert medical and scientific analysis and interpretation of data from ongoing studies and in the literature • Prepare publications and presentations for scientific meetings and congresses Essential Skills/Experience: • Fully qualified physician (MD or MD PhD) with clinical experience in pulmonology (preferred), infectious disease, or other relevant specialty  • 1-3 years of experience in clinical drug development, preferably from pharma industry  • Strong understanding of clinical trials methodology with experience in the design, execution, and interpretation of clinical studies (e.g., medical monitoring, data cleaning, clinical study report writing) • Excellent teamwork and cross-functional collaboration skills • Ability to communicate effectively in clinical team settings • Excellent verbal and written communication skills (including giving presentations) in English • Demonstrated AI/digital mindset and experience applying AI-enabled and generative AI tools to support clinical development activities (e.g., data analysis, medical writing, clinical trial operational efficiency) • Must demonstrate high integrity • Be office based at an AstraZeneca site at least 3 days a week Desirable Skills/Experience : • Additional clinical experience in vaccines and/or monoclonal antibodies • Named Investigator on several clinical trials • 1-3 years of pharmaceutical industry knowledge and experience • Progressed medicines into first time in human Phase 1, Phase 2 delivery of proof of principle, and Phase 3 pivotal efficacy studies • Experience with Translational programs moving from preclinical to first in human studies and interpretation of immunological assay results • Significant and consistent peer-reviewed publication track record The annual base pay for this position ranges from $249,827.20 - $374,740.80. Hourly and salaried non-exempt employees will also be paid overtime pay when working qualifying overtime hours. Base pay offered may vary depending on multiple individualized factors, including market location, job-related knowledge, skill

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