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BIOTECHMULTICHANNELCMO & CLINICAL

Cold email campaign for clinical research — multi-channel campaign

6 steps over 40 days. 5 emails, 1 LinkedIn message.

Charles Perret, founder of devlo

Charles Perret

Founder of devlo.ch · March 2026

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Interested prospects

The 6 keys in the sequence

5 emails, 1 LinkedIn message — over 40 days.

LinkedInDay 1LinkedIn login
{% spin %}{% variation %}Hello{% variation %}Dear{% variation %}Hi{% endspin %} {{firstName}}, {{linkedinnote}} The LinkedIn note begins with: “Your LinkedIn post about… Your LinkedIn profile shows that… Your interview OR your article OR your blog post… My colleague {{SalesRep}} told me about… … I’m delighted to get in touch with you.” --- → Audio message (sent 6 days after the LinkedIn connection request was accepted): Delighted to get in touch with you. My colleague {{SalesRep}} sent you an email regarding our biometrics services. Over 350 sponsors trust us as a specialist provider of data management and statistics, and I was wondering if you are currently overseeing any clinical trials? --- → Message mentioning colleagues’ names (sent 7 days later): Hello {{firstName}}, would it be best to contact your colleagues {{colleaguename1}} or {{colleaguename2}} to discuss biometric services related to the implementation of your clinical development programmes? --- → Follow-up message (sent 5 days later): {{firstName}}, I understand that it’s not certain whether you need help with trial design, data management or biostatistics at the moment. Please don’t hesitate to contact me if you’d like to know why sponsors prefer us to their former biometrics service provider. Best regards Other LinkedIn response templates → Sent manually if the prospect replies with an inconclusive message that interrupts the sequence {{firstName}}, my colleague {{SalesRep}} has sent you an email explaining why sponsors choose us for their clinical trial, data management, biostatistics and other services. [...] (full content available on request)
EmailDay 1Email #2
Subject: phone call {{firstname}}
{% assign ampm = "now" | date: "%P" %}{% if ampm contains "am" %}Good morning{% else %}Good morning{% endif %} {{firstName}}, {{icebreaker}} Over 350 organisations trust us as their biometric partner for clinical trial design, data management and biostatistical services. Our clients were determined to optimise their clinical trial timelines and data processing workflows to improve their cost-effectiveness. They sought advice on data integrity and regulatory compliance. They also needed to ensure their data was ready for submission. [ClientCompanyName] handled the data management for our Phase I/II clinical trials, and I am very satisfied with this collaboration, says the clinical project manager at a Swiss biotechnology company. Is it worth providing a little more context during a brief phone call, or is that off-topic? Kind regards, {{signature}}
Email7 days laterEmail #3
Subject: Talk to {{colleaguename1}} or {{colleaguename2}}
{% spin %}{% variation %}Hello{% variation %}Dear{% variation %}Hi{% endspin %} {{firstName}}, Would it be best to contact your colleague {{colleaguename1}} or {{colleaguename2}} regarding your clinical development programmes? I understand you’re busy, but I wouldn’t want to miss the opportunity to work with {{companyName}}. We’d like to see if it’s worth providing valuable support and helping to further {{company name}}’s mission. My to-do list below reminded me to write to you 😊 Have a great day {{signature}}
Email5 days laterEmail #4
{% spin %}{% variation %}Hello{% variation %}Dear{% variation %}Hi{% endspin %} {{firstName}}, We understand that time and budget are limited, that regulatory hurdles are significant, and that the design of clinical trials is becoming increasingly complex. You and your colleagues will be impressed to see how our experts have helped our clients successfully complete their clinical trials. Would you have a little time this week to discuss this over the phone?
Email8 days laterEmail #5
{% assign ampm = "now" | date: "%P" %}{% if ampm contains "am" %}Good morning{% else %}Good morning{% endif %} {{firstName}}, What do you think of my suggestion: finding out how pharmaceutical companies such as {{companyName}} have successfully completed their clinical trials by collecting data of the highest quality? Our clients consistently express their satisfaction at no longer having to deal with inexperienced staff. To prove this to you, we’d like to invite you to a [ProductName] lasting up to 5 hours to discuss {{companyname}}’s clinical development plan. This introductory call with our team of experts is 100% free. First of all, would you be interested in a virtual coffee to find out a bit more? {{signature}}
Email6 days laterEmail #6
{% assign ampm = "now" | date: "%P" %}{% if ampm contains "am" %}Good morning{% else %}Good morning{% endif %} {{firstName}}, Our director [Director_Name] and I have been trying to get in touch with you. We thought you might be interested in finding out how our clients have solved Why do so many Phase III clinical trials fail? (webinar) Accelerated Authorisations (AA): not so fast! (white paper) The ultimate guide to clinical data management (eBook) Would it be possible to have a brief telephone chat? If you’re not interested, please let me know; that’s perfectly understandable. Kind regards, {{signature}} Objections: “We work with a CRO offering a full range of services (both a clinical CRO and a biometric CRO): Working with a dedicated biometric CRO ensures the highest quality for your clinical trial programmes in terms of data management and biostatistics. Background: Large CROs excel at managing clinical operations, such as patient recruitment and site monitoring. Biometric CROs ({{clientCompanyName}}), on the other hand, specialise in statistical analysis, data management and clinical data reporting. A partnership with both a clinical CRO and a biometric CRO gives you access to both these aspects. “We already have a partner”: “So you are already receiving the appropriate support from your clinical partner, a CRO specialising in biometrics, and if so, how is the collaboration with them going?”​ “Isn’t it worth exploring the other options available to find out what’s out there and at what cost?” “Have you noticed smooth communication between the clinical teams and those responsible for data management?” [...] (full content available on request)

Why this sequence works

This 9-touch sequence over 40 days is designed for the highly specialised field of clinical research, targeting CEOs, CMOs and medical directors at biotech companies. The complexity of the CRO sales cycle requires a patient and educational approach.

The testimonial from a Clinical Project Leader at a Swiss biotech company and the reference to "350+ organisations that trust us" establish strong credibility. In the world of clinical research, trust and track record are the key criteria for selecting a CRO.

The offer of a "5-hour introductory call, 100% free" (Touch #5) is an exceptional value proposition. For a biotech company evaluating a CRO partner, five hours of free consultancy represents significant tangible value that justifies the decision-maker’s investment of time.

What you can learn from this campaign

  • Offer a valuable introductory call. Five hours of free consultancy represents tangible value for a biotech company.
  • Use specific case studies. Case studies on randomisation, the pharmaceutical supply chain and biostatistics.
  • Address the objection raised by the existing CRO. "Most of our clients were working with another CRO before they came to us."
  • Combine LinkedIn voice notes and emails. The audio message played after the connection is accepted is a key differentiator.

When to use this sequence

CRO services and clinical biometrics

Data management, biostatistics, clinical trial design — this module is the perfect fit for you.

Targeting CEOs and CMOs of biotech companies

The key target audience is clinical trial decision-makers in biotech companies.

International market (USA and Europe)

The section covers the two main markets in clinical research.

Long-term consultative sales

The 40-day cycle is well suited to complex decision-making in the pharmaceutical sector.

Who can use this sequence?

CROs and clinical service providers

If you offer data management, biostatistics or trial design services.

SDRs targeting biotech companies

The bilingual scripts (EN/FR) and objection handling are ready to use.

Clinical data platforms

If your solution makes it easier to manage clinical trial data.

Regulatory affairs consultants

Adapt the workflow to suit your compliance and FDA/EMA submission processes.

Frequently Asked Questions

How can you approach biotech companies to offer CRO services?

The key is to demonstrate clinical expertise right from the first email. Mentioning 350+ sponsors and including a testimonial from a Swiss client establishes credibility. Biotech companies are looking for a reliable partner for their trials — trust takes precedence over price. The offer of a free consultation (5 hours) is the key differentiator.

Why a 40-day programme for the clinical sector?

Decisions regarding CRO partnerships are complex and involve several decision-makers (CEO, CMO, Medical Director). A 40-day period allows time for information to circulate internally. The nine-step engagement sequence maintains a presence without being intrusive, featuring educational content (webinars, white papers) that delivers value.

How should you deal with objections from the existing CRO?

The response is already prepared: "Most of our clients were working with another CRO before they came to us." Then offer an objective comparison ("unless you’re sure you’re getting the best service"). This respectful yet challenging approach works well with clinical decision-makers.

Want a customised sequence for your industry?

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Last updated: March 2026