B

Bristol Myers Squibb

Global biopharma researching, developing, delivering medicines

Clinical Research Associate

Full-TimeDeadline 12/31/26
No salary listed
Junior, Mid
Bachelor's
Bellheim, Germany+1 moreMore locations: Stuttgart, Germany
In PersonOn-site roles with regional travel; German residency or work authorization required.

About the job

Requirements
  • Bachelor’s degree required, preferably within life sciences or equivalent
  • Valid driver’s license (as locally required)
  • Clinical Research Associate: 2-3 years of relevant clinical research experience, able to work independently, demonstrates proficiency in all aspects of the role
  • Experience in the drug discovery/development process
  • Knowledge and understanding of clinical research processes, regulations and methodology
  • Understands clinical landscape with practical knowledge of a variety of medical settings and medical records management
  • Working knowledge of ICH/GCP Guidelines and applicable local laws and regulations (that govern clinical trials, with the ability to apply regulatory requirements to ensure compliance in clinical research activities
  • Analytical thinking/critical thinking skills; capable of using technology to analyze diverse and complex data sets, identify issues, trends, and outliers to develop effective solutions
  • Demonstrated adaptability and a growth mindset by quickly learning and applying new technologies, embracing evolving methodologies, and remaining open to innovative ways of working in a dynamic environment
  • Organization and time management skills
  • Ability to build, maintain and strengthen relationships even under pressure and/or in difficult situations with internal and external stakeholders
  • Good verbal and written communication skills (both in English and local language)
  • Foundational level of disease understanding and awareness (how the protocol fits in current landscape, standard of care, etc.)
  • Proven ability to work independently with a high degree of autonomy, proactively managing tasks and seeking opportunities for continuous learning
  • Ability to manage multiple protocols, across multiple therapeutic areas, which may require travel, based upon assigned site location and/or geographic territory
  • Proficient in navigating and utilizing multiple clinical systems (e.g., CTMS, eDC, eTMF, RBQM dashboards) to identify and resolve issues, support site performance, and ensure data integrity
  • Software that must be used independently and without assistance: Clinical Trial Management Systems (CTMS); Electronic Data Capture Systems (eDC); Electronic Trial Master File (eTMF); RBM tools and platforms (e.g., Veeva, Medidata, CluePoints)
Responsibilities
  • Conduct site qualification, initiation, routine monitoring and close-out visits across all trial phases in accordance with the Site Monitoring Plan, ensuring adherence to protocol, BMS Standard Operating Procedures (SOPs) and ICH GCP
  • Maintain the ethical and scientific integrity of clinical trials by verifying data within electronic systems and paper records (as applicable) to ensure the accessibility, completeness and accuracy of data submitted by study sites
  • Conduct site qualification, initiation, routine monitoring and close-out visits across all trial phases in accordance with the Site Monitoring Plan, ensuring adherence to protocol, BMS Standard Operating Procedures (SOPs) and ICH GCP
  • Monitor site adherence to ICH GCP and local regulations, including compliance with the principles of ALCOA to maintain data integrity and reliability. Where required, provide training and support to site staff to uphold these standards and ensure patient safety. Participate in sponsor and/or Health Authority audits and inspections as applicable.
  • Cultivate and sustain effective relationships with internal cross-functional teams and external partners, including vendors, clinical sites, and key stakeholders. Serve as the organization’s representative for clinical trials at the site level.
  • Motivate and influence sites to meet study objectives, including enrolment and retention goals.
  • Communicate effectively, adapting to meet the needs of different stakeholders, utilizing the most appropriate communication style and method.
  • Prepare and submit written reports, both monitoring and administrative, in a timely, accurate, concise, professional and objective manner
  • Assess potential Investigators and their sites to ensure sufficient resources and capabilities to conduct clinical trials. May identify new potential Investigators and/or sites through ongoing collaborations with internal and external stakeholders during the site feasibility and selection process.
  • Demonstrate understanding and proficiency working with targeted, centralized, remote and risk based monitoring approaches
  • Identify, assess, and prioritize risks at the site and study level and support sites in mitigating issues, including implementing mitigation strategies based on risk indicators
  • Utilize strong analytical skills to evaluate site data and operational metrics, including ability to adjust monitoring strategies based on data trends and site performance
  • Where applicable, perform Unblinded Site Monitor activities to protect the blind of the study by acting as secondary monitoring source separate from the blinded monitor
  • Accountable for the review, reconciliation, and oversight of study drug/IMP. May support study drug/IMP label translation needs as applicable.
  • Involvement in Regulatory Compliance audit/inspection process, as needed. This includes the development and implementation of site corrective and preventive actions.
  • In specific instances, may support start-up and submission related activities, including ICF reviews and collection of documents to/from site.
  • Support provision of access to relevant BMS and vendor systems is available for clinical trial site personnel and ensures internal BMS systems are kept up to date for site monitoring activities.
  • Support coordination of site activities related to database locks to ensure timelines are met as required locally.
  • Perform timely site closure activities when all required protocol visits and follow-up are completed.
Desired Qualifications
  • None

About the company

Bristol Myers Squibb develops and sells medicines for serious diseases, focusing on cancer, immune system disorders, and cardiovascular conditions. Its work starts with research and development to create new therapies, which are then approved by regulators before being used by doctors and patients; the company also offers generic versions and supports biosimilars to expand access. BMS differentiates itself with a broad portfolio of innovative medicines alongside affordable options and a strong emphasis on ESG and regulatory engagement. The goal is to improve patient health by delivering effective, affordable medicines and advancing sustainable healthcare globally.

Company Size

10,001+

Company Stage

IPO

Headquarters

Lawrence Township, New Jersey

Founded

1887

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Simplify's Take

What believers are saying

  • BMS raised 2026 revenue guidance to $49 billion-$50 billion on July 30, 2026.
  • Houston's $2.3 billion campus adds nearly 500 jobs and supports a $40 billion U.S. plan.
  • BMS kept ALOFT-IPF on track for 4Q26 after independent monitoring recommended continuation.

What critics are saying

  • BMS disclosed 265 New Jersey layoffs on September 22, 2026, after 1,700-plus cuts.
  • Milvexian's atrial fibrillation readout slipped into Q1 2027, delaying Eliquis replacement hopes.
  • Revlimid fell 49% in Q2 2026; if Eliquis weakens, BMS faces a growth vacuum.

What makes Bristol Myers Squibb unique

  • BMS spans oncology, immunology, and cardiovascular with Opdivo, Eliquis, and Cobenfy.
  • Houston's 2026 modular campus supports small molecules, biologics, and antibody-drug conjugates.
  • Opdivo Qvantig conversion reached about 15% in July 2026, strengthening franchise stickiness.

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Benefits

Flexible Work Hours

Hybrid Work Options

Professional Development Budget

Growth & Insights and Company News

Headcount

6 month growth

↑ 7%

1 year growth

↑ 7%

2 year growth

↑ 7%
BioSpace
Oct 1st, 2026
BMS reports liver injury events in lung disease program, with key readout near.

BMS reports liver injury events in lung disease program, with key readout near. October 1, 2026 | Bristol Myers Squibb will soon release Phase 3 data for admilparant that could make or break Contineum Therapeutics' rival product. But reports of a death due to liver injury in the pharma's program have caused some unease about the drug class. Bristol Myers Squibb has amended the protocol for a Phase 3 clinical program testing pulmonary fibrosis candidate admilparant, reporting multiple cases of liver injuries, including one death. But the study has yet to be fully unblinded, leaving the cause of the events unclear at this time, the company said. The disclosure unsettled investors in Contineum Therapeutics, which is developing a similar product, due to fears about a potential class-wide effect. The issue came to light this week, despite the protocol change being made in May. BMO Capital Markets analysts flagged the issue in a Wednesday note, suggesting that too many questions remain unanswered to determine if admilparant caused the liver issues. "A limited number" of liver events have been observed in the Phase 3 ALOFT program, BMS confirmed to BioSpace in an emailed statement. Most were mild, transient and linked to other medical conditions or in patients taking other medications that have known liver risk factors. There was one death, reportedly due to multi-organ failure after acute liver injury, but it's unclear whether the patient was taking admilparant because BMS is still blinded to the data. "Without identifying whether the patient was on treatment, investors cannot clearly assume this acute hepatic injury-driven death was tied to admilparant or even associated with treatment," BMO wrote. The protocol amendment flagged interstitial lung disease and multiple other comorbidities as complicating factors related to the death. BMS is barreling toward a clinical trial readout that an H.C. Wainwright analyst believes could contribute to the return of mergers between mega-cap drugmakers. September 2, 2026 The independent data monitoring committee, however, has been reviewing incoming unblinded data regularly and has recommended that the trial continue, BMS said. Another committee has been created to specifically look at potential liver injury, BMO noted. The ALOFT program features multiple pulmonary fibrosis indications, with a near term readout for the Phase 3 ALOFT-IPF study in idiopathic pulmonary fibrosis "likely to be significant" for BMS, BMO said. The firm remains cautious about that readout, which is expected in the fourth quarter. "Limited information on potential drug-related liver injury raises overall risk of ALOFT program, but data remains on track for a 4Q26 disclosure," BMO said. While analysts note that admilparant is one of BMS' most important near-term catalysts, BMO said fourth quarter data for the secondary stroke prevention candidate milvexian is a higher priority. A class action? BMS investors are not alone in awaiting the ALOFT-IPF readout, with the protocol amendment raising some questions about the lysophosphatidic acid receptor 1 (LPA1-R) class. Contineum Therapeutics is developing a rival therapy called PIPE-791, currently in a Phase 2 trial called PROPEL-IPF. BMS' protocol amendment sent Contineum's shares down sharply on Wednesday, Stifel said in an investor note. The stock has since recovered to $13.42 as of Thursday morning, slightly above its closing price Tuesday. The ALOFT-IPF outcome "is core to the CTNM thesis for PIPE-791," Stifel said. But the firm does not believe the evidence so far suggests that the LPA1-R mechanism is the culprit. While expressing disappointment, William Blair analysts were unsurprised by the Phase II failure, having assigned the VISTA study a high level of risk given the "mixed" performance of a similar drug in a prior multiple sclerosis study. November 21, 2025 Contineum's therapy also has a different molecular makeup and much lower dose, so Stifel downplayed any readthrough. William Blair caught up with Contineum CEO Carmine Stengone, who similarly brushed off concerns. "We continue to believe there is minimal on-mechanism risk here and that this potential signal is molecule and dose specific, if anything, which bodes well for PIPE-791 differentiation," the firm wrote in a Thursday morning note. If BMS' forthcoming readout is positive, William Blair believes it will help derisk the LPA1-R mechanism in IPF. The indication is currently served by Boehringer Ingelheim's Ofev and Jascayd and Legacy Pharma's Esbriet. Stengone estimated a total addressable market of $10-14 billion, if PIPE-791 clears clinical trials and becomes standard-of-care. Annalee Armstrong is an award-winning biopharma journalist covering the business of drug development. She has been a journalist for more than 18 years, covering the pharmaceutical and biotech industry for the last eight. She is senior editor at BioSpace and curates the Biopharm Executive newsletter every Wednesday. You can reach her at [email protected]. Follow her on LinkedIn.

Biotech Insider
Sep 30th, 2026
Bristol Myers Squibb edges up as its income case returns.

Bristol Myers Squibb edges up as its income case returns. Bristol Myers Squibb was flagged as a high-yield healthcare holding for income portfolios as its shares traded at 63.00 on Sept. 30, up 0.22% while the Dow slipped. Bristol Myers Squibb shares traded at 63.00, up 0.22% on the day, on Sept. 30, 2026, as Investor's Business Daily named the drugmaker a high-yield, stable-fundamentals pick for income investors. Bristol Myers Squibb (BMY) was singled out on Tuesday as a candidate for income-focused portfolios in healthcare, a sector that has spent much of this cycle overshadowed by technology. The stock changed hands at 63.00, up 0.22% from the previous close of 62.86, as of the last trade at 17:40 GMT on Sept. 30, 2026. The argument, laid out by Investor's Business Daily, is straightforward: investors hunting for a high yield backed by stable fundamentals in healthcare do not need to look past Bristol Myers Squibb. It is a familiar pitch for large-cap pharma, and it deserves to be examined on its own terms rather than accepted as a category truth. What the tape said on the day. The session was a quiet one for the stock but a revealing one for the market around it. Bristol Myers traded between 62.87 and 64.13, a band of roughly 2.0% between the day's low and high - active enough to show real two-way interest, but the close-to-close move of 0.22% suggests the buying and selling largely cancelled out. Context matters here. The S&P 500, proxied by SPY, was at $767.52, up 0.43% from a previous close of $764.20. The Nasdaq 100 tracker QQQ sat at $743.26, up 0.72%. The Dow 30 proxy DIA was the outlier, down 0.20% at $511.88. That split - growth indices higher, the blue-chip average lower - is the pattern that has repeatedly left large-cap pharma looking cheap relative to the broader market and has kept dividend yields in the sector elevated. A stock that edges up while the Dow slips is doing its job for the kind of investor this thesis targets. Income buyers are not looking for the day's biggest percentage gain. They are looking for a share price that does not destroy the value of the coupon they are collecting. Why yield alone is the wrong test. The phrase "high yield" in equities is a warning as often as it is an invitation. A dividend yield rises for two very different reasons: the company raises its payout, or the share price falls. The second is far more common among the highest-yielding names in any screen, and it is how income investors end up owning businesses in structural decline while telling themselves they are being paid to wait. That is why the second half of the IBD framing - stable fundamentals - carries most of the weight. For a large pharmaceutical company, stability comes down to a handful of testable things: * Cash conversion. Whether operating cash flow comfortably exceeds the cash sent out as dividends, rather than being topped up by debt or asset sales. * Revenue concentration. How much of the top line depends on a small number of drugs, and how close those drugs are to losing exclusivity. * Pipeline replacement. Whether late-stage candidates and recent approvals can plausibly fill the gap when older products go generic. * Balance-sheet room. Whether the company can fund acquisitions to buy growth without putting the dividend in the queue behind creditors. Those four questions are the whole ballgame for pharma income stocks, and they are also the reason the sector trades at a discount to the market. The uncertainty is not about this quarter's earnings. It is about what the revenue base looks like several years out, which is precisely the horizon an income investor cares about. The patent cliff is the variable that matters. Those four questions are the whole ballgame for pharma income stocks, and they are also the reason the sector trades at a discount to the market. Every major drugmaker lives on a schedule set by patent expirations. Exclusivity ends, generics or biosimilars enter, and a product that generated billions can lose the majority of its revenue in a short span. The market prices this risk in advance, which is one mechanism by which a pharma dividend yield gets pushed up without the company doing anything wrong. For an investor evaluating Bristol Myers on income grounds, the question is not whether the current dividend is covered - for a company of this size it almost certainly is today - but whether it remains covered through the next expiration cycle. That depends on how much of the revenue base is exposed, over what timeframe, and what is behind it in development. Those are answerable questions from company filings, and any reader acting on a high-yield thesis should answer them before buying rather than after. It is also worth noting what a dividend is not: a contract. Boards cut payouts when cash flow demands it, and pharmaceutical companies have done so when major products fell off patent without adequate replacement. The historical record of a rising dividend is evidence of intent, not a guarantee of continuation. How the trade fits a portfolio. The practical case for holding a large-cap drugmaker in an income sleeve is diversification of risk, not maximisation of yield. Healthcare demand is relatively insensitive to the economic cycle, which means revenue tends not to collapse alongside consumer spending or industrial activity. In a portfolio where dividend income is concentrated in banks, energy and utilities, a pharma holding is exposed to a genuinely different set of variables: regulatory decisions, clinical outcomes and drug pricing policy rather than interest rates and commodity prices. The offsetting risk is that those variables are lumpy. A single failed trial readout or an adverse regulatory decision can reprice a large-cap pharma stock in a day by more than a year's dividend income. That is the trade an income investor in this sector is actually making, and it is not the same as the low-drama profile the "stable fundamentals" label implies. What to watch from here. Three things will determine whether this thesis ages well. First, the next dividend declaration and any change to the rate - a raise confirms confidence, a hold signals caution. Second, the company's own disclosure of expected revenue erosion from loss of exclusivity, which sets the bar the pipeline must clear. Third, the relative performance of healthcare against the growth indices. As long as QQQ is outrunning the Dow, pharma yields are likely to stay generous - and investors will keep having to work out whether that generosity is compensation for risk or a genuine mispricing. Key facts. * BMY last trade: 63.00, +0.22% (as of 17:40 GMT, Sept. 30, 2026) * Day range: 62.87 - 64.13; previous close 62.86 * Benchmarks: SPY $767.52 (+0.43%), QQQ $743.26 (+0.72%), DIA $511.88 (-0.20%) * Thesis: High yield plus stable fundamentals in healthcare, per Investor's Business Daily Frequently asked questions. What was Bristol Myers Squibb's share price on Sept. 30, 2026? Bristol Myers Squibb (BMY) last traded at 63.00, a gain of 0.22% from the previous close of 62.86, as of 17:40 GMT on Sept. 30, 2026. The stock moved between 62.87 and 64.13 during the session, a modest band that indicated active two-way trading without a decisive directional move. Why is Bristol Myers Squibb being discussed as an income stock? Investor's Business Daily presented the drugmaker as a choice for investors seeking a high dividend yield combined with stable fundamentals within healthcare. Large-cap pharmaceutical companies typically generate substantial operating cash flow and pay consistent dividends, which places them in the same portfolio category as utilities and banks for income-focused buyers. Does a high dividend yield always signal a good investment? No. A dividend yield rises either because a company increases its payout or because its share price falls. The second cause is far more common among the highest-yielding stocks on any screen. Investors should check whether operating cash flow comfortably covers the dividend before treating a high yield as an opportunity rather than a warning. What is a pharmaceutical patent cliff? A patent cliff is the point at which a drug loses market exclusivity and generic or biosimilar competitors can enter. Revenue from that product can fall sharply within a short period. Because major drugmakers often depend on a handful of products, the timing of these expirations is one of the largest variables in valuing a pharma stock. How did the broader market perform that day? Growth indices outperformed blue chips. The S&P 500 proxy SPY rose 0.43% to $767.52 and the Nasdaq 100 tracker QQQ gained 0.72% to $743.26, while the Dow 30 proxy DIA fell 0.20% to $511.88. Bristol Myers edging higher against a declining Dow was a relative positive for the session. What should an income investor check before buying a pharma dividend stock? Four things: whether operating cash flow exceeds dividends paid, how concentrated revenue is in a few products, how close those products are to patent expiry, and whether the balance sheet has room to fund acquisitions without threatening the payout. All four are disclosed in company filings and should be verified before purchase.

U.S. Securities and Exchange Commission
Sep 30th, 2026
Joint Press Release

Bristol-Myers Squibb and AstraZeneca Expand Diabetes Alliance Through Bristol-Myers

APAC News Network
Sep 28th, 2026
Shilpi Sinha appointed GCO India Head at Johnson & Johnson.

Shilpi Sinha appointed GCO India Head at Johnson & Johnson. Summarize with: New Delhi, Sep 28(APAC Media): Shilpi Sinha has joined Johnson & Johnson Innovative Medicine as Director, Country Head - GCO India. In this role, Sinha will lead the company's Global Clinical Operations (GCO) function in India, covering areas related to clinical operations and research activities. Shilpi Sinha's New Role Sinha brings more than two decades of experience in clinical research, clinical operations, project management and quality management. Her appointment adds to Johnson & Johnson's leadership team supporting clinical development activities in India. Before joining Johnson & Johnson Innovative Medicine, Sinha spent more than 14 years at Bristol Myers Squibb. She most recently served as Director, Country Head RCO India. Experience In Clinical Research Sinha has worked across several areas of clinical research and operations during her career. At Bristol Myers Squibb, she held roles involving clinical operations, project management and quality functions. Earlier, she worked at Parexel as Project Quality Lead. She began her career with Quintiles as a Clinical Team Lead. With experience across pharmaceutical and clinical research organisations, Sinha's new role will focus on the company's Global Clinical Operations activities in India. Her career spans more than 20 years across clinical trials, research operations and quality management. Summarize with:

Yahoo Finance
Sep 24th, 2026
Bristol Myers Squibb vs Pfizer: which healthcare stock is a better buy in 2026?

Bristol Myers Squibb and Pfizer, two pharmaceutical giants facing patent cliffs on blockbuster drugs, are taking divergent approaches to growth. Bristol Myers focuses on oncology and immunology whilst Pfizer leverages pandemic-era cash for acquisitions in high-growth areas like obesity treatments. Bristol Myers reported FY 2025 revenue of $48.2 billion, down 0.2% year-over-year, with net income of $7.1 billion and a 14.6% net margin. The company maintains a debt-to-equity ratio of 2.6x and generated $12.8 billion in free cash flow. Pfizer's FY 2025 revenue totalled $62.6 billion, declining 1.6%, with net income of $7.8 billion and a 12.4% net margin. Recent acquisitions include Seagen and Metsera, positioning the firm in oncology and obesity markets. Both companies partner with distributors and maintain global operations across multiple therapeutic areas.