Clinical Research Jobs at Amgen with Visa Sponsorship
Amgen's Clinical Research function spans oncology, cardiology, and rare disease programs, with roles ranging from clinical operations and data management to regulatory affairs. Amgen has a well-established infrastructure for supporting international hires, making it a realistic target for candidates who need visa sponsorship.
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Join Amgen’s Mission of Serving Patients
At Amgen, if you feel like you’re part of something bigger, it’s because you are. Our shared mission—to serve patients living with serious illnesses—drives all that we do.
Since 1980, we’ve helped pioneer the world of biotech in our fight against the world’s toughest diseases. With our focus on four therapeutic areas –Oncology, Inflammation, General Medicine, and Rare Disease– we reach millions of patients each year. Amgen is advancing a broad and deep pipeline of medicines to treat cancer, heart disease, inflammatory conditions, rare diseases, and obesity and obesity-related conditions. As a member of the Amgen team, you’ll help make a lasting impact on the lives of patients as we research, manufacture, and deliver innovative medicines to help people live longer, fuller happier lives.
Our award-winning culture is collaborative, innovative, and science based. If you have a passion for challenges and the opportunities that lay within them, you’ll thrive as part of the Amgen team. Join us and transform the lives of patients while transforming your career.
Clinical Research Medical Director
What you will do
Let’s do this. Let’s change the world. In this vital role you will support Clinical Development in Prostate cancer.
- Supporting the development, execution and communication of the global scientific/medical evidence plan
- Supporting cross-functional and global collaborations to integrate broad medical, scientific, and commercial input into the development program
- Supporting the development of key scientific external relationships with opinion leaders
- Participating and providing clinical input into safety and regulatory interactions
- Provide clinical/scientific input during the development and execution of clinical trials
- Interpret clinical trial data
- Participate in safety assessments
- Participate in interactions with regulatory agencies
- Author CSRs, publications and regulatory submissions
- Develop key opinion leaders and make scientific presentation at advisory boards, key scientific meetings and external committee meetings as delegated by Global Development Leader
- Identify new clinical research opportunities
- Support in-licensing and out-licensing activities and partner relationships
- Support product lifecycle management for new indications as directed by Global Development Leader
- Provide clinical content input to:
- Regulatory interactions and documents
- Safety interactions and documents
- Materials to be used in Scientific Affairs
- Materials to be used by the Commercial Organization
What we expect of you
We are all different, yet we all use our unique contributions to serve patients. The clinical development professional we seek has these qualifications.
Basic Qualifications:
MD or DO degree from an accredited medical school
AND
2 years of clinical research experience and/or basic science research
Preferred Qualifications:
- 5+ years of clinical research experience and/or basic science research combined with clinical teaching and patient care activities, particularly in GU Oncology (prostate cancer)
- Clinical research experience in the biopharmaceutical industry (biotech, pharmaceutical or CRO company)
- In-depth understanding of the scientific method and clinical applications based on medical, scientific and practical rationale
- Familiarity with concepts of clinical research and clinical trial design, including biostatistics
- Sound scientific and clinical judgment
- Knowledge of Good Clinical Practices (GCP), FDA and EMEA/CHMP regulations and guidelines, and applicable international regulatory requirements
- Ability to effectively present ideas and document complex medical/clinical concepts in both written and oral communication
- Demonstrated ability as a medical expert in a complex matrix environment
- History of solving problems while exhibiting superior judgment and a balanced, realistic understanding of issues
What you can expect of us
As we work to develop treatments that take care of others, we also work to care for your professional and personal growth and well-being. From our competitive benefits to our collaborative culture, we’ll support your journey every step of the way.
The expected annual salary range for this role in the U.S. (excluding Puerto Rico) is posted. Actual salary will vary based on several factors including but not limited to, relevant skills, experience, and qualifications.
In addition to the base salary, Amgen offers a Total Rewards Plan, based on eligibility, comprising of health and welfare plans for staff and eligible dependents, financial plans with opportunities to save towards retirement or other goals, work/life balance, and career development opportunities that may include:
- A comprehensive employee benefits package, including a Retirement and Savings Plan with generous company contributions, group medical, dental and vision coverage, life and disability insurance, and flexible spending accounts
- A discretionary annual bonus program, or for field sales representatives, a sales-based incentive plan
- Stock-based long-term incentives
- Award-winning time-off plans
- Flexible work models where possible. Refer to the Work Location Type in the job posting to see if this applies.
Apply now and make a lasting impact with the Amgen team.
In any materials you submit, you may redact or remove age-identifying information such as age, date of birth, or dates of school attendance or graduation. You will not be penalized for redacting or removing this information.
Application deadline
Amgen does not have an application deadline for this position; we will continue accepting applications until we receive a sufficient number or select a candidate for the position.
Sponsorship
Sponsorship for this role is not guaranteed.
As an organization dedicated to improving the quality of life for people around the world, Amgen fosters an inclusive environment of diverse, ethical, committed and highly accomplished people who respect each other and live the Amgen values to continue advancing science to serve patients. Together, we compete in the fight against serious disease.
Amgen is an Equal Opportunity employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability status, or any other basis protected by applicable law.
We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation.

Join Amgen’s Mission of Serving Patients
At Amgen, if you feel like you’re part of something bigger, it’s because you are. Our shared mission—to serve patients living with serious illnesses—drives all that we do.
Since 1980, we’ve helped pioneer the world of biotech in our fight against the world’s toughest diseases. With our focus on four therapeutic areas –Oncology, Inflammation, General Medicine, and Rare Disease– we reach millions of patients each year. Amgen is advancing a broad and deep pipeline of medicines to treat cancer, heart disease, inflammatory conditions, rare diseases, and obesity and obesity-related conditions. As a member of the Amgen team, you’ll help make a lasting impact on the lives of patients as we research, manufacture, and deliver innovative medicines to help people live longer, fuller happier lives.
Our award-winning culture is collaborative, innovative, and science based. If you have a passion for challenges and the opportunities that lay within them, you’ll thrive as part of the Amgen team. Join us and transform the lives of patients while transforming your career.
Clinical Research Medical Director
What you will do
Let’s do this. Let’s change the world. In this vital role you will support Clinical Development in Prostate cancer.
- Supporting the development, execution and communication of the global scientific/medical evidence plan
- Supporting cross-functional and global collaborations to integrate broad medical, scientific, and commercial input into the development program
- Supporting the development of key scientific external relationships with opinion leaders
- Participating and providing clinical input into safety and regulatory interactions
- Provide clinical/scientific input during the development and execution of clinical trials
- Interpret clinical trial data
- Participate in safety assessments
- Participate in interactions with regulatory agencies
- Author CSRs, publications and regulatory submissions
- Develop key opinion leaders and make scientific presentation at advisory boards, key scientific meetings and external committee meetings as delegated by Global Development Leader
- Identify new clinical research opportunities
- Support in-licensing and out-licensing activities and partner relationships
- Support product lifecycle management for new indications as directed by Global Development Leader
- Provide clinical content input to:
- Regulatory interactions and documents
- Safety interactions and documents
- Materials to be used in Scientific Affairs
- Materials to be used by the Commercial Organization
What we expect of you
We are all different, yet we all use our unique contributions to serve patients. The clinical development professional we seek has these qualifications.
Basic Qualifications:
MD or DO degree from an accredited medical school
AND
2 years of clinical research experience and/or basic science research
Preferred Qualifications:
- 5+ years of clinical research experience and/or basic science research combined with clinical teaching and patient care activities, particularly in GU Oncology (prostate cancer)
- Clinical research experience in the biopharmaceutical industry (biotech, pharmaceutical or CRO company)
- In-depth understanding of the scientific method and clinical applications based on medical, scientific and practical rationale
- Familiarity with concepts of clinical research and clinical trial design, including biostatistics
- Sound scientific and clinical judgment
- Knowledge of Good Clinical Practices (GCP), FDA and EMEA/CHMP regulations and guidelines, and applicable international regulatory requirements
- Ability to effectively present ideas and document complex medical/clinical concepts in both written and oral communication
- Demonstrated ability as a medical expert in a complex matrix environment
- History of solving problems while exhibiting superior judgment and a balanced, realistic understanding of issues
What you can expect of us
As we work to develop treatments that take care of others, we also work to care for your professional and personal growth and well-being. From our competitive benefits to our collaborative culture, we’ll support your journey every step of the way.
The expected annual salary range for this role in the U.S. (excluding Puerto Rico) is posted. Actual salary will vary based on several factors including but not limited to, relevant skills, experience, and qualifications.
In addition to the base salary, Amgen offers a Total Rewards Plan, based on eligibility, comprising of health and welfare plans for staff and eligible dependents, financial plans with opportunities to save towards retirement or other goals, work/life balance, and career development opportunities that may include:
- A comprehensive employee benefits package, including a Retirement and Savings Plan with generous company contributions, group medical, dental and vision coverage, life and disability insurance, and flexible spending accounts
- A discretionary annual bonus program, or for field sales representatives, a sales-based incentive plan
- Stock-based long-term incentives
- Award-winning time-off plans
- Flexible work models where possible. Refer to the Work Location Type in the job posting to see if this applies.
Apply now and make a lasting impact with the Amgen team.
In any materials you submit, you may redact or remove age-identifying information such as age, date of birth, or dates of school attendance or graduation. You will not be penalized for redacting or removing this information.
Application deadline
Amgen does not have an application deadline for this position; we will continue accepting applications until we receive a sufficient number or select a candidate for the position.
Sponsorship
Sponsorship for this role is not guaranteed.
As an organization dedicated to improving the quality of life for people around the world, Amgen fosters an inclusive environment of diverse, ethical, committed and highly accomplished people who respect each other and live the Amgen values to continue advancing science to serve patients. Together, we compete in the fight against serious disease.
Amgen is an Equal Opportunity employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability status, or any other basis protected by applicable law.
We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation.
See all 39+ Clinical Research at Amgen jobs
Sign up for free to unlock all listings, filter by visa type, and get alerts for new Clinical Research at Amgen roles.
Get Access To All JobsTips for Finding Clinical Research Jobs at Amgen Jobs
Align your credentials to specialty occupation standards
Amgen's Clinical Research roles typically require a degree in life sciences, nursing, pharmacy, or a related clinical field. Before applying, confirm your degree maps directly to the role title, since USCIS evaluates specialty occupation fit at the petition stage.
Target roles that match your visa category
Amgen sponsors multiple visa types across Clinical Research, but not every role suits every category. F-1 OPT applicants should prioritize openings aligned with their STEM-designated program, since a direct field match strengthens both the STEM extension and any future H-1B petition.
Research Amgen's therapeutic area hiring cycles
Clinical Research hiring at Amgen tracks closely with pipeline milestones in oncology and cardiometabolic disease. Roles in clinical operations and trial monitoring tend to open during Phase II and III expansion, so timing your application to those cycles improves your odds of landing a sponsored position.
Use Migrate Mate to filter open Clinical Research roles
Not every job board surfaces visa-sponsored positions accurately. Use Migrate Mate to browse Amgen's current Clinical Research openings filtered by sponsorship type, so you're applying to roles where your visa category is already an expected part of the hiring process.
Clarify H-1B timeline with your recruiter early
If you're currently on OPT and need H-1B sponsorship, raise it before the offer stage. USCIS cap-subject H-1B petitions must be filed in April for an October 1 start, so both you and Amgen's immigration team need enough lead time to coordinate the lottery registration and petition filing.
Prepare for PERM labor certification if targeting a Green Card
Amgen supports EB-2 and EB-3 pathways for Clinical Research professionals, which require DOL PERM labor certification before USCIS adjudicates the immigrant petition. Understanding where your priority date falls in the Visa Bulletin helps you evaluate your long-term timeline before accepting an offer.
Clinical Research at Amgen jobs are hiring across the US. Find yours.
Find Clinical Research at Amgen JobsFrequently Asked Questions
Does Amgen sponsor H-1B visas for Clinical Research roles?
Yes, Amgen sponsors H-1B visas for Clinical Research positions. Because most cap-subject H-1B petitions must be filed by April 1 for an October 1 start date, you'll need to align your offer timeline accordingly. Amgen has an established immigration program and works with outside counsel to manage filings, but you should raise your visa status early in the recruitment process so the team can plan around USCIS deadlines.
How do I apply for Clinical Research jobs at Amgen?
Applications go through Amgen's careers portal, where you can filter by function and location. Clinical Research roles are listed under categories like Clinical Development, Clinical Operations, or Regulatory Affairs depending on the specific position. Migrate Mate also aggregates Amgen's sponsored Clinical Research openings, which lets you filter by visa type before applying so you're targeting roles where sponsorship is already part of the hiring plan.
Which visa types does Amgen commonly use for Clinical Research hires?
Amgen sponsors H-1B, E-3, TN, J-1, and F-1 OPT and CPT for Clinical Research roles, along with EB-2 and EB-3 immigrant visa pathways for longer-term hires. E-3 is available to Australian citizens only, and TN applies to Canadian and Mexican nationals in qualifying occupations. The right category depends on your nationality, degree field, and where you are in your career stage.
What qualifications does Amgen expect for Clinical Research positions?
Most Clinical Research roles at Amgen require a bachelor's degree or higher in a life sciences, pharmacy, nursing, or related clinical field, with the specific requirement varying by role level. Senior clinical operations or data management positions often require several years of trial experience in a CRO or biopharmaceutical setting. For H-1B eligibility, your degree must map to a specialty occupation directly related to the duties of the specific role.
How long does the visa sponsorship process typically take for a Clinical Research offer at Amgen?
Timeline depends on visa type. H-1B cap-subject petitions require lottery registration in March and a filing window in April, with employment starting October 1 at the earliest. E-3 and TN petitions can move faster, often within four to eight weeks from offer to approval. EB-2 and EB-3 green card pathways involve DOL PERM labor certification followed by a USCIS I-140 petition, which can span one to two years before reaching the immigrant visa stage.
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