Senior Clinical Research Associate

Medasource; Philadelphia (Philadelphia County); Remote; USD 75,000 - 100,000; Full time

Job summary

A leading company in life sciences is seeking a Sr. Clinical Research Associate to oversee clinical studies and ensure compliance with regulatory requirements. The ideal candidate will have a strong background in clinical research, excellent communication skills, and the ability to work independently. This role involves traveling and working with clinical sites to support the enrollment of study participants.

Benefits

Medical insurance

Vision insurance

401(k)

Qualifications

• Bachelor's in a related field with a focus on natural science.
• Five years of clinical research experience.
• Strong verbal and written communication skills.

Responsibilities

• Monitor clinical studies for compliance and accuracy.
• Coordinate with study teams and enroll clinical sites.
• Train site personnel on protocol compliance.

Skills

Written communication

Verbal communication

Interpersonal skills

Analytical skills

Organizational skills

Education

Bachelor’s degree in natural science, pre-medicine, nursing, bioengineering or related field

Tools

Word processing software

Relevant clinical applications

Job description

Direct message the job poster from Medasource

Job Title: Sr. Clinical Research Assoicate

Location: Remote with Travel required (Philly)

Client: Large Life Sciences Company

Start Date: 7/07/2025

Duration: 12-month contract with the possibility for extension

Job Duties:

· Monitors clinical studies at sites in an assigned territory (and others as requested) to ensure compliance with applicable regulatory requirements, Good Clinical Practice, and accuracy standards inclusive of site initiation, periodic, and close-out visits.

· Ensures both regulatory and clinical protocol compliance is maintained for all assigned clinical projects. This may include, but is not limited to:

o Reviewing data and source documentation from investigational sites for accuracy and completeness

o Ensuring adverse events and protocol deviations are reported in an efficient manner

o Ensuring that device complaints and malfunctions are reported according to Policies and Procedures

o Resolving and/or facilitating resolution of problems including identification of cause and actions to prevent reoccurrence

· Coordinates with study teams, field clinical engineers or designee and specialists to:

o Enroll sites into new and ongoing clinical studies

o Facilitate enrollment of study subjects via site coordinators

o Facilitate resolution of data queries and action items at clinical sites

· Promptly reports the findings of monitoring visits according to processes.

· Collaborates with in-house teams to ensure complete submission of study documents.

· Participates in conference calls and training sessions.

· Trains site personnel to ensure compliance with the study protocol and local regulations.

· Mentors less experienced clinical team members as requested.

· Demonstrates a high level of written and verbal communication skills with internal and external customers.

Minimum Qualifications:

· A Bachelor’s degree from an accredited university or college. Preferably with an academic focus in natural science, pre-medicine, nursing, bioengineering, or a related academic field.

· Superb understanding of all aspects of clinical research.

· Minimum five years clinical research experience.

· Must have demonstrated strong written and verbal communication, interpersonal, presentation, analytical, organizational skills.

· Ability to interpret basic clinical data, to meet deadlines as well as the ability to communicate effectively with all levels of employees.

· Basic personal computer skills including a working familiarity with word processing software and relevant clinical applications.

· The ability to work independently and function within a dynamic, global team environment.

· The ability to exchange straightforward information, ask questions, and check for understanding.

Preferred Qualifications:

· Strong preference for prior clinical monitoring experience.

· A general familiarity with cardiac, vascular, and/or neuromodulation technologies.

· Previous related experience in a medical device/pharmaceutical company or relevant clinical experience in a clinical/hospital environment.

· Certification by an industry-recognized professional society (i.e. Society of Clinical Research Associates (SoCRA) or Association of Clinical Research Professionals (ACRP) or accredited institution

Seniority level

• Seniority level

  Mid-Senior level

Employment type

• Employment type

  Contract

Job function

• Job function

  Health Care Provider

• Industries

  Hospitals and Health Care and Pharmaceutical Manufacturing

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Inferred from the description for this job

Medical insurance

Vision insurance

401(k)

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