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Clinilabs

Proposal Writer -Remote

$70K - $90K/yr

... with Clinilabs corporate strategy, metrics, style and branding parameters. • Ensures effective communication among internal stakeholders throughout the process so that the strategy drives the ...

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How much do clinilabs jobs pay per hour?

As of Jun 10, 2026, the average hourly pay for clinilabs in the United States is $18.86, according to ZipRecruiter salary data. Most workers in this role earn between $15.38 and $19.95 per hour, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a Clinical Research Associate at Clinilabs, and why are they important?

To thrive as a Clinical Research Associate at Clinilabs, you need a solid background in life sciences or a related field, clinical trial experience, and knowledge of Good Clinical Practice (GCP) guidelines. Familiarity with electronic data capture (EDC) systems, regulatory documentation, and industry certifications such as ACRP or SOCRA are typically required. Excellent attention to detail, organizational skills, and effective communication enable strong collaboration with study sites and sponsors. These skills are essential to ensure clinical trials are conducted safely, ethically, and in compliance with regulatory standards.

What types of teams and professionals will I typically collaborate with as a Clinilabs clinical research staff member?

At Clinilabs, clinical research staff commonly work alongside a multidisciplinary team that includes physicians, nurses, laboratory technicians, data managers, and regulatory specialists. Collaboration is essential for coordinating study protocols, ensuring participant safety, and maintaining regulatory compliance. You'll also interact with sponsors, monitors, and sometimes directly with study participants, fostering a dynamic and communicative work environment. This teamwork not only supports high-quality research but also offers opportunities to learn from various healthcare and research professionals.

What is the difference between Clinilabs vs Clinical Research Coordinator?

AspectClinilabsClinical Research Coordinator
Required CredentialsBachelor's degree, clinical research experience, sometimes certificationsBachelor's degree often required, certifications like CCRP beneficial
Work EnvironmentResearch clinics, hospitals, pharmaceutical companiesResearch sites, hospitals, clinics
Employer & Industry UsagePharmaceutical companies, CROs, research institutionsHospitals, research centers, CROs
Common Search & ComparisonYesYes

Clinilabs typically refers to a research organization conducting clinical trials, often hiring research staff with specific experience. A Clinical Research Coordinator (CRC) manages clinical trials at research sites. While both roles involve clinical research, Clinilabs staff may work within the organization, whereas CRCs are often employed at trial sites. Understanding these differences helps job seekers identify the right opportunities in the clinical research industry.

What is Clinilabs?

Clinilabs is a contract research organization (CRO) that specializes in providing clinical research services to the pharmaceutical, biotechnology, and medical device industries. They conduct clinical trials to test new drugs and medical treatments, focusing on areas such as neuroscience, sleep disorders, and psychiatry. Clinilabs supports the development of new therapies by managing and monitoring studies, ensuring regulatory compliance, and collecting data to determine the safety and efficacy of investigational products.
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What states have the most Clinilabs jobs? States with the most job openings for Clinilabs jobs include:
What job categories do people searching Clinilabs jobs look for? The top searched job categories for Clinilabs jobs are:
Clinilabs jobs near you
Infographic showing various Clinilabs job openings in the United States as of June 2026, with employment types broken down into 100% Full Time. Highlights an 50% In-person, and 50% Remote job distribution, with an average salary of $39,233 per year, or $18.9 per hour.
Proposal Writer -Remote

Proposal Writer -Remote

Clinilabs

Remote

$70K - $90K/yr

Full-time

Posted yesterday

Job description

JOB SUMMARY
The Proposal Writer will create winning strategies highlighting key selling points and execution strategies based on input from the business development team and business unit leadership in Global Clinical Operations, Clinical Research Unit, and Corelab. The Proposal Writer will develop customized executive summaries and targeted proposal text directly related to the therapeutic area, scope of work, and phase of development. Where appropriate, the Proposal Writer will seek input and contributions from vendors for integration into the proposal.
RESPONSIBILITIES
• Work collaboratively with internal stakeholders (e.g. business development, business unit leadership, budget team) and external stakeholders (e.g. scientific advisors, vendors, consultants) to develop strategies that effectively articulate customer needs critical to generating new business awards.
• Conducts qualitative and quantitative research to create customized and compelling business development documents focused on client solutions that highlight company differentiation, innovation and operational strategy.
• Produces high quality, customer-specific deliverables aligned with Clinilabs corporate strategy, metrics, style and branding parameters.
• Ensures effective communication among internal stakeholders throughout the process so that the strategy drives the project, and the final document(s) achieves its goals.
• Meets deadlines consistently by establishing priorities and target dates for document contributions, review, and approval by key stakeholders including executive leadership.
• Works with administrative members of the business development team to maintain a current database of responses and text in Clinilabs proposal development software.
• Other duties as assigned
TRAVELING
Attendance at annual summit and/or sales meeting may be required.
Salary Range: $70,000-$90,000 annually. Final compensation is based on skills, experience, location, and overall expertise.
Requirements
REQUIRED EDUCATION, KNOWLEDGE, SKILLS AND ABILITIES
• BA/BS in life sciences, professional or creative writing, marketing, communications, business administration or a related discipline.
• Experience in the CRO, pharmaceutical, or biotechnology industry including technical writing, communications, or marketing experience.
• Minimum of two (2) years of CRO clinical proposal writing experience.
• Knowledge of clinical budget development is preferred.
• Must have knowledge of the drug development process including functional operations and regulatory guidelines and directives.
• Demonstrated ability to evaluate scientific and business information (e.g. trial protocols, investigator brochures, RFP documents) and use conclusions to write persuasive and technical sales documents.
• Proficiency in Microsoft Office Suite (Word, Excel, Outlook, SharePoint and PowerPoint).
• Experience with proposal development software preferred.
• Energetic, proactive, highly analytical and self-motivated with a passion for innovation and continuous improvement.
• Ability to work under pressure in a deadline driven environment while maintaining accuracy, quality, and detail.
• Resourceful and proactive with proven ability to handle multiple competing priorities simultaneously.
• Strong orientation toward customer service and high level of personal responsibility and quality.

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