Amgen Limited Posted September 25, 2026

Study Start-up Manager

Aberdeen, United Kingdom Full time
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Amgen Limited is the source of truth for this posting and owns the application process. We surface normalized context and market comparison you won't find on the original listing.

About this opportunity

Career Category

Clinical

Job Description

Job Description

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. 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.

Study Start Up Hub – Study Start-up Mgr

What you will do

Let’s do this. Let’s change the world. In this vital role you will drive the planning and execution of clinical study start-up activities, ensuring trials are launched efficiently, compliantly, and to the highest quality standards.

Lead the planning and delivery of clinical study start-up activities from global to local, ensuring timelines, quality, budget, and regulatory compliance are met.

Own and manage study start-up plans and milestones, maintaining oversight of progress and resolving issues to keep delivery on track.

Act as the primary point of contact for cross-functional start-up teams, driving clarity of roles, accountability, and collaboration.

Identify, assess, and mitigate risks proactively, contributing to study risk assessments and ensuring timely study start.

Partner closely with Study Delivery Leads, managers, and local teams, providing clear updates, solutions, and escalation where needed.

Apply strong operational and regulatory knowledge (e.g. ICH-GCP, submissions and start-up processes) to enable high-quality execution.

Manage internal resources and external suppliers to ensure efficient and compliant delivery of start-up activities.

Contribute to continuous improvement by sharing expertise, mentoring colleagues, and developing best practices within the SSU hub.

What we expect of you

We are all different, yet we all use our unique contributions to serve patients. The candidate we seek is an individual with the following qualifications.

Basic Qualifications:

Pharma Expertise: Requires pharma and clinical trial processes and operations expertise; no relevant therapeutic knowledge required

Management Experience: Requires experience leading and managing global teams and project management experience

Tech Skills:  No prior Veeva experience required

Doctorate degree OR

Master’s degree and 3 years of clinical execution experience OR

Bachelor’s degree and 5 years of clinical execution experience OR

Associate’s degree and 10 years of clinical execution experience OR

High school diploma / GED and 12 years of clinical execution experience

In addition to meeting at least one of the above requirements, you must have experience directly managing people and/or leadership experience leading teams, projects, programs, or directing the allocation of resources.  Your managerial experience may run concurrently with the required technical experience referenced above

Preferred Qualifications:

5 years work experience in life sciences or medically related field, including 3 years of biopharmaceutical clinical research experience obtained working on clinical trials in a biotech, pharmaceutical or CRO company

Experience working in global clinical trial teams across multiple geographies

Experience with risk-based monitoring models / risk-based quality management, and/or clinical site management

PMP Certification

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 annual base salary range for this opportunity in the U.S. is [Talent Acquisition to input market pay range].

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:

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 and bi-annual company-wide shutdowns

Flexible work models, including remote work arrangements, where possible

Apply now

for a career that defies imagination

Objects in your future are closer than they appear. Join us.

careers.amgen.com

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.

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Job details

Seniority
Manager
Function
Clinical Development
Therapeutic area
Not listed
Location
Aberdeen, United Kingdom
Employment type
Full time

How this role compares

Computed from every other active Clinical Development role in our database, not just this employer's listings.

We currently track 418 comparable Manager Clinical Development roles across 65 biopharma companies.

418Comparable roles tracked
395Currently active
65Companies hiring similar roles
38Countries represented

Salary context

134 of 418 peers report a salary range (USD, annualized)

Peers share this role's job function and a matching or adjacent seniority level -- not necessarily the same therapeutic area or country.

This roleSubject Not listed on this posting
Lowest disclosed · Associate, Clinical Data Systems · AbbVie $58,656/yr – $103,500/yr
Highest disclosed · Associate Director, Clinical Development · Gilead Sciences, Inc. $210,375/yr – $272,250/yr
Peer group range $81,078 – $241,313 (median $180,500)

Where these roles are based

Top locations among the 418 comparable roles

United States194
India54
United Kingdom25
China20
Japan13
Poland11

+ 32 more countries

Seniority mix

418 of 418 peers have a known seniority level

Manager255
Associate Director114
Associate49

Therapeutic area mix

35 of 418 peers have a known therapeutic area; the rest are genuinely unlabeled, not hidden

Oncology19
Immunology7
Ophthalmology2
Neuroscience2
Cardiovascular / CVRM2
Respiratory2
Dermatology & Aesthetics1

Similar opportunities

The closest matches from our peer group, ranked by how similar they are, not how well you'd qualify for them -- treat this as market context, not a guaranteed shortlist; a weak match is labeled as one below.

60%similar
Regeneron UK Limited Uxbridge1, United Kingdom Manager
Same function Same seniority Same country
60%similar
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60%similar
IQVIA London, United Kingdom Manager
Same function Same seniority Same country
60%similar
IQVIA Reading, United Kingdom Manager
Same function Same seniority Same country
60%similar
IQVIA Reading, United Kingdom Manager
Same function Same seniority Same country
60%similar
Labcorp Harrogate, United Kingdom Manager
Same function Same seniority Same country

Notify me about similar jobs

Get an email when we spot other openings like this one – same job function, comparable seniority, roles you'd actually want to see.

Or follow a whole field: get every new Clinical Development job in the United Kingdom, and choose locations and companies.

How we calculate "similar"

No black box, no LLM guesswork: a deterministic score built from four normalized attributes. Here's this role's own peer group at different match levels, so you can see the mechanism, not just the result.

Every comparison starts from the same 100-point budget: 25 for working in the same function, 40 for the same therapeutic area, 20 for the same or adjacent seniority, 15 for the same country. A dimension we can't confirm on both sides contributes nothing, never a guess, never a free pass.

60%
Manager, Medical Affairs Operations - Uxbridge, UK
Regeneron UK Limited · Uxbridge1, United Kingdom · Manager
Function Therapeutic area Seniority Country
60%
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IQVIA · London, United Kingdom · Manager
Function Therapeutic area Seniority Country
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Global Study Manager - 1year contract
Labcorp · Harrogate, United Kingdom · Manager
Function Therapeutic area Seniority Country
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Global Clinical Project Manager - Vendor Management Expert (home-based in Europe)
IQVIA · Reading, United Kingdom · Manager
Function Therapeutic area Seniority Country
Unmatched or unknown dimensions score exactly the same: 0 points, never a partial guess. A role we know almost nothing about beyond its function bottoms out at 25%; it never inflates to 100% just because there's little to compare against. Seniority uses a defined ladder (Associate → Manager → Associate Director → Senior → Principal → Director → Senior Director → Executive/VP) so "Director" and "Senior Director" count as adjacent, but "Director" and "Executive/VP" do not.