Clinical Research Associate - Entry Level

About the job

Our successful Clinical Research Associates possess varied backgrounds in medical and other sciencerelated healthcare fields. Individuals who have succeeded in the CRA role include:

• Nurses
• Dieticians
• Pharmacy Technicians
• Pharmaceutical/Device Sales Representatives
• Biotech Engineers
• PhD/Pharm.D candidates
• Health and Wellness Coordinators
• Research Assistants.

PACE MEDPACE CRA TRAINING PROGRAM

No research experience is needed as Medpace provides comprehensive initial and ongoing training unmatched by other CROs. Through our PACE Training Program you will join other Professionals Achieving CRA Excellence:

PACE provides the platform to effectively and confidently carry out your duties enhance your current abilities and ultimately help you become a highfunctioning independent Medpace CRA.

PACE will prepare you by developing your CRA skills through interactive discussions and hands on jobrelated exercises and practicums.

To supplement your inhouse and fieldbased training you may also participate in other clinical research departmental core rotations learning other aspects of the drug/device development and approval process.

UNEXPECTED REWARDS

This role takes you on a journey through travel and excitement which will allow you to make a difference on a large scale through the enhancement of pharmaceuticals and medical devices. The CRA position provides many other distinctive advantages including:

Dynamic working environment with varying responsibilities dayto day

Expansive experience in multiple therapeutic areas

Work within a team of therapeutic and regulatory experts

Defined CRA promotion and growth ladder with potential for mentoring and management advancements

Competitive pay and opportunity for significant travel bonus

Responsibilities

• As a CRA Entry you will specifically be responsible for the following:
• Conduct qualification initiation monitoring and closeout visits for research sites in compliance with the approved protocol;
• Communication with the medical site staff including coordinators clinical research physicians and their site staff;
• Verifying adequate investigator qualifications training and resources including facilities laboratories equipment and staff;
• Medical record and research source documentation verification against case report form data including informing the site staff of any entry errors ensuring good documentation practices are being adhered to and communicating protocol deviations appropriately per SOPs GCP and applicable regulatory requirements;
• Verification that the investigator is enrolling only eligible subjects;
• Regulatory document review;
• Medical device and/or investigational product/drug accountability and inventory;
• Verification and review of adverse events serious adverse events concomitant medications and corresponding illnesses to confirm accurate data reporting in accordance with the protocol;
• Assessing the clinical research sites patient recruitment and retention success and offering suggestions for improvement;
• Completion of monitoring reports and followup letters which includes providing summaries of the significant findings deviations deficiencies and recommended actions to secure compliance.

Qualifications

• Minimum of a bachelors degree; Health or life science related field preferred;
• Candidate with Clinical Research Coordinator experience is an advantage:
• Willing to travel approximately 6080% nationally;
• Familiarity with Microsoft Office; and
• Strong communication and presentation skills a plus.

Lifelancer ( ) is a talenthiring platform in Life Sciences Pharma and IT. The platform connects talent with opportunities in pharma biotech health sciences healthtech data science and IT domains.

Please use the below Lifelancer link for job application and quicker response.

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Remote Work :

No