Literature Surveillance Sr. Associate
3 days ago
The Literature Surveillance Sr. Associate is responsible for daily surveillance, curation, and compliant distribution of medical and scientific literature across Amgen's therapeutic areas. This role ensures timely delivery of accurate literature alerts and curated content that inform internal stakeholders, support medical strategy, and comply with Amgen's Global Healthcare Compliance SOPs.
Working closely with Scientific Communications and Medical Content Leads, the Literature Surveillance Associate reviews publications, applies metadata, generates alerts, and contributes to the accuracy, efficiency, and quality of Amgen's global literature surveillance process.
Roles & Responsibilities:
Conducting daily monitoring of scientific literature using ReadCube Papers, PubMed, journal websites, and clinical guidelines (e.g., NCCN, ASCO, ESMO)
Screening and curating articles across multiple therapeutic areas and applying metadata including citation details, document type, product/competitor associations, RADAR categories, and priority tags
Generating, formatting, and distributing literature alerts to subscribed stakeholders, and maintaining distribution lists and subscriptions, as needed
Retrieving full-text articles through Papers, RightFind, or Amgen libraries; escalating requests requiring budget approval; and ensuring copyright and transfer-of-value compliance
Updating and maintaining internal trackers documenting articles screened, curated, alerted, or discarded
Collaborating with Medical Content Leads and other stakeholders to refine searches and tagging criteria based on feedback
Supporting ad hoc searches and contributing to refinement of surveillance strategies
Remaining adaptable to emerging tools, automation, and digital innovations supporting literature workflows
Basic Qualifications and Experience:
Degree and 5-9 years of directly related industry experience; experience in literature review, medical writing, publications, or related role (academic or industry)
Functional Skills:
Preferred Qualifications:
Bachelor's degree in life sciences, pharmacy, biomedical sciences, or a related field
Strong scientific and analytical skills to assess relevance of peer-reviewed literature
Proficiency with literature management tools (e.g., ReadCube Papers, PubMed, RightFind, SharePoint)
Excellent attention to detail and ability to follow established guidelines and SOPs
Strong written and verbal communication skills
Prior experience in medical communications, publication management, or competitive intelligence
Familiarity with therapeutic areas such as oncology, cardiovascular, bone, rare diseases, and inflammation
Experience with regulatory-driven surveillance and clinical guideline monitoring
Working knowledge of compliance, copyright, and transfer-of-value reporting in literature sharing
Competencies:
Team orientation: Collaborates effectively across global teams and time zones
Continuous improvement mindset: Proactively identifies opportunities to streamline processes
Scientific curiosity: Eager to learn about new therapeutic areas and medical research
Attention to detail: Ensures accuracy in curation, tagging, and metadata management
Time management: Prioritizes daily high-volume workload and meets strict timelines
Adaptability: Operates effectively in a dynamic, fast-paced environment
Ethics & compliance: Maintains integrity and adherence to compliance in all work
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.
In addition to the base salary, Amgen offers competitive and comprehensive Total Rewards Plans that are aligned with local industry standards.
Apply now
for a career that defies imagination
Objects in your future are closer than they appear. Join us.
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 with 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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