Clinical Research Associate

CTTX Health

Cambridge, MAJobPosted 7mo agoSeen in employer's feed 6 days ago

Cambridge, MAJobNo compensation foundPosted 7mo agoSeen in employer's feed 6 days ago

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At a glance

Compensation

No compensation found

Location

Cambridge, MA

Work Authorization

Not specified

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Job overview

CTTX Health is hiring a Clinical Research Associate. The Clinical Research Associate will join a fast-growing biotech company focused on advancing innovative therapies in neuroscience. This role involves conducting site initiation, monitoring, and close-out visits to ensure trials meet quality standards. The associate will also review and verify study data, collaborate with site staff and cross-functional teams, and identify and escalate protocol deviations or safety concerns.

Key focus areas include Conduct site initiation, monitoring, and close-out visits., Review and verify study data for accuracy and completeness., and Collaborate with site staff and cross-functional teams..

Successful candidates bring Bachelor's In Life Sciences/Nursing/Pharmacy and 3+ Years CRA Experience. Important skills include ICH-GCP, FDA Regulations, Communication, Organization, Problem-Solving, and Rare-Disease Trials. Preferred (not required): CNS Trials.

Skills & qualifications

RequiredNice to have

Skills

ICH-GCPFDA RegulationsCommunicationOrganizationProblem-SolvingCNS TrialsRare-Disease Trials

Qualifications

Bachelor's in Life SciencesBachelor's in NursingBachelor's in PharmacyBachelor's in Related Field3+ Years CRA Experience3+ Years Site Monitoring ExperienceWillingness to Travel Up to 50–75%Advanced Degree

Full job description

Are you passionate about clinical research and ready to make an impact on patients’ lives? We’re looking for a Clinical Research Associate (CRA) to join a fast-growing biotech company (confidential) that’s advancing innovative therapies in neuroscience.

What You’ll Do:

Conduct site initiation, monitoring, and close-out visits to ensure trials meet the highest quality standards.
Review and verify study data for accuracy and completeness.
Collaborate with site staff and cross-functional teams to solve challenges and keep trials on track.
Identify and escalate any protocol deviations, safety concerns, or data issues.

Requirements

What We’re Looking For:

Bachelor’s in Life Sciences, Nursing, Pharmacy, or related field (advanced degree a plus).
3+ years of CRA or site monitoring experience.
Strong knowledge of ICH-GCP and FDA regulations.
Excellent communication, organization, and problem-solving skills.
Willingness to travel as needed (up to 50–75%).

Extra Credit:

Experience with CNS or rare-disease trials.

Benefits

Amazing benefits package starting day one!

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