Alpha Clinical Development is seeking exceptional leaders to join our team across various locations in the USA. We’re hiring for key roles in Regulatory Affairs, Clinical Development, and Pharmacovigilance, offering opportunities to shape the future of healthcare innovation. If you’re a seasoned professional with a passion for advancing science, check out our open positions below!
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Open Positions
We’re looking for talented individuals to fill the following leadership roles:
1. Associate Director/Director Regulatory Affairs
Job Details
| Details | Information |
|---|---|
| Location | Pacific Side, USA (Remote role) |
| Contact | Send resume to rafia.ishfaq@acdlimited.com |
Qualifications & Experience
- Education: Master’s degree in Life Sciences or related field (Ph.D. or advanced degree preferred)
- Experience: 8–12+ years in regulatory affairs with strong FDA submission experience (BLA, NDA, etc.)
- Preferred: Oncology experience and ability to interact effectively with FDA and other health authorities
2. Executive Director Clinical Development
Job Details
| Details | Information |
|---|---|
| Location | Bay Area / San Francisco (On-site) |
| Contact | Send resume to mawraa.mohammad@acdlimited.com |
Qualifications & Experience
- Education: MD (Doctor of Medicine) degree
- Experience: 10–15 years in clinical development and strategic leadership in Immunology and Oncology
- Skills: Proven experience leading clinical programs from inception to regulatory submission; strong knowledge of regulatory requirements and clinical research best practices
3. Executive Director/VP Regulatory Affairs – Medical Device
Job Details
| Details | Information |
|---|---|
| Location | Bay Area (Hybrid/On-site preferred, 6-month contract with potential extension) |
| Contact | Send resume to aleema.zahra@acdlimited.com |
Qualifications & Experience
- Education: Advanced degree (Ph.D., MS, or equivalent) in Life Sciences, Engineering, Regulatory Affairs, or related field preferred
- Experience: 15+ years in regulatory affairs within the medical device industry
- Skills: In-depth knowledge of FDA regulations (510(k), PMA, IDE, De Novo), EU MDR, ISO 13485, and global frameworks; proven success in regulatory submissions and agency interactions
4. Vice President Pharmacovigilance
Job Details
| Details | Information |
|---|---|
| Location | Boston, MA (Hybrid role) |
| Contact | Send resume to nadeem.sherazi@acdlimited.com |
Qualifications & Experience
- Education: MD or equivalent degree, Board certification in a relevant specialty
- Experience: 10+ years in pharmacovigilance and drug safety, including 5+ years in a leadership role
- Skills: Strong vendor management; experience with regulatory filings (especially BLAs); preferred expertise in liver, endocrine, or cardiometabolic therapies (e.g., MASH)
How to Apply
- Prepare: Update your resume to highlight your relevant experience and qualifications.
- Submit: Send your resume to the respective contact email listed for each role.
- Act Fast: These are high-impact positions—don’t miss your chance to join our team!
Why Alpha Clinical Development?
At Alpha Clinical Development, we’re driving breakthroughs in clinical research and regulatory excellence. Whether you’re shaping regulatory strategy, leading clinical programs, or ensuring drug safety, you’ll work with a team dedicated to transforming lives through science. Join us in one of our key U.S. locations and make a difference in healthcare innovation.
We’re excited to meet our next leaders! Apply today and let’s advance the future of medicine together.
