Clinical Research Associate - Entry (Home-based)

Job Title: Clinical Research Associate - Entry (Home-based) Job Location: UNAVAILABLE, Malaysia Job Location Type: Remote Job Contract Type: Full-time Job Seniority Level: We are currently seeking a full-time, Clinical Research Associate Entry to join our Clinical Monitoring team in the Malaysia. This role is a vital part of the team to accomplish tasks and projects that are instrumental to the company's success. For those with medical and/or health/life science interest and background who want to explore the research field and be part of a team bringing pharmaceutical and medical devices to market - this could be the right opportunity for you! PACE® – MEDPACE CRA TRAINING PROGRAMNo 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 high-functioning independent Medpace CRA.PACE® will prepare you by developing your CRA skills through interactive discussions and hands on job-related exercises and practicums.To supplement your in-house and field-based training you may also participate in other clinical research departmental core rotations, learning other aspects of the drug/device development and approval process. UNEXPECTED REWARDSThis 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 day-to dayExpansive experience in multiple therapeutic areasWork within a team of therapeutic and regulatory expertsDefined CRA promotion and growth ladder with potential for mentoring and management advancementsCompetitive pay and opportunity for significant travel bonus Responsibilities 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 site’s patient recruitment and retention success and offering suggestions for improvement;Completion of monitoring reports and follow-up letters, which includes providing summaries of the significant findings, deviations, deficiencies, and recommended actions to secure compliance. QualificationsBachelor’s degree in Health or Life Science related field preferred;At least 2 years of prior study coordinator experience is preferred;Willing to travel approximately 60-80% nationally;Familiarity with Microsoft® Office; andStrong communication and presentation skills a plus. Medpace OverviewMedpace is a full-service clinical contract research organization (CRO) providing phase l-lV clinical development services to the biotechnology, pharmaceutical, and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through the advancement of clinical research. We leverage in-country regulatory and therapeutic expertise across all major therapeutic areas including oncology, cardiology, metabolic, endocrinology, central nervous system, and anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, we employ more than 6,500 people across 40+ countries. Why Medpace?When you join Medpace, you become part of an innovative team that brings cutting-edge therapies to market while building a meaningful and rewarding career focused on scientific excellence and improving patient outcomes around the world through continuous learning and cross-functional collaboration. Purpose-Driven WorkWork alongside physicians, scientists, and industry-leading experts committed to advancing the global development of medical therapeutics through clinical research excellence Collaborative CultureContribute to an interactive team environment that empowers decision making, creative thinking, and continuous learning through open communication and mutual trust.Leadership throughout Medpace is both accessible and approachable Continuous Growth & DevelopmentOffice based environment with on-site mentorsDefined career paths with clear advancement opportunitiesIndustry renowned onboarding and training programs designed to accelerate professional developmentOngoing training and continuous learning opportunities throughout your careerAn environment that encourages employees to influence change, contribute ideas, and grow quickly Other Employee BenefitsCompetitive compensation programs that recognize and reward performanceComprehensive health, wellness, retirement, and PTO benefitsOffice based culture with occasional WFH that provides flexibility for eligible positions after trainingCompany-sponsored social events Please note benefits may vary based on country. What to Expect NextA Medpace team member will review your application and if your profile matches our current needs, you will be contacted for an interview. While we review all applications carefully, we are unable to respond to every applicant, and only candidates selected for interviews will be contacted.This job is curated by Lifelancer. Lifelancer is a talent-hiring platform in Life Sciences, Pharma and IT. The platform connects talent with opportunities in pharma, biotech, health sciences, healthtech and IT domains. Please apply via Lifelancer platform to get connected to the application page and to find similar roles.

Job Title: Clinical Research Associate - Entry (Home-based)

Job Title:

Job Location: UNAVAILABLE, Malaysia

Job Location:

Job Location Type: Remote

Job Location Type:

Job Contract Type: Full-time

Job Contract Type:

Job Seniority Level:

Job Seniority Level:

We are currently seeking a full-time, Clinical Research Associate Entry to join our Clinical Monitoring team in the Malaysia. This role is a vital part of the team to accomplish tasks and projects that are instrumental to the company's success. For those with medical and/or health/life science interest and background who want to explore the research field and be part of a team bringing pharmaceutical and medical devices to market - this could be the right opportunity for you!

We are currently seeking a full-time, Clinical Research Associate Entry to join our Clinical Monitoring team in the Malaysia. This role is a vital part of the team to accomplish tasks and projects that are instrumental to the company's success. For those with medical and/or health/life science interest and background who want to explore the research field and be part of a team bringing pharmaceutical and medical devices to market - this could be the right opportunity for you!For those with medical and/or health/life science interest and background who want to explore the research field and be part of a team bringing pharmaceutical and medical devices to market - this could be the right opportunity for you!

PACE® – MEDPACE CRA TRAINING PROGRAM

PACE® – MEDPACE CRA TRAINING PROGRAMPACE®®– 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:

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:®PPAACCEE

• PACE® provides the platform to effectively and confidently carry out your duties, enhance your current abilities and ultimately help you become a high-functioning independent Medpace CRA.

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

• PACE® will prepare you by developing your CRA skills through interactive discussions and hands on job-related exercises and practicums.

PACE® will prepare you by developing your CRA skills through interactive discussions and hands on job-related exercises and practicums.®

• To supplement your in-house and field-based training you may also participate in other clinical research departmental core rotations, learning other aspects of the drug/device development and approval process.

To supplement your in-house and field-based 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

UNEXPECTED REWARDSUNEXPECTED 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:

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 day-to day

Dynamic working environment, with varying responsibilities day-to day

• Expansive experience in multiple therapeutic areas

Expansive experience in multiple therapeutic areas

• Work within a team of therapeutic and regulatory experts

Work within a team of therapeutic and regulatory experts

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

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

• Competitive pay and opportunity for significant travel bonus

Competitive pay and opportunity for significant travel bonusResponsibilities

• Conduct qualification, initiation, monitoring, and closeout visits for research sites in compliance with the approved protocol;

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;

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;

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;

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;

Verification that the investigator is enrolling only eligible subjects;

• Regulatory document review;

Regulatory document review;

• Medical device and/or investigational product/drug accountability and inventory;

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;

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 site’s patient recruitment and retention success and offering suggestions for improvement;

Assessing the clinical research site’s patient recruitment and retention success and offering suggestions for improvement;

• Completion of monitoring reports and follow-up letters, which includes providing summaries of the significant findings, deviations, deficiencies, and recommended actions to secure compliance.

Completion of monitoring reports and follow-up letters, which includes providing summaries of the significant findings, deviations, deficiencies, and recommended actions to secure compliance.Qualifications

• Bachelor’s degree in Health or Life Science related field preferred;

Bachelor’s degree in Health or Life Science related field preferred;

• At least 2 years of prior study coordinator experience is preferred;

At least 2 years of prior study coordinator experience is preferred;At least 2 years of prior study coordinator experience is preferred;

• Willing to travel approximately 60-80% nationally;

Willing to travel approximately 60-80% nationally;

• Familiarity with Microsoft® Office; and

Familiarity with Microsoft® Office; and

• Strong communication and presentation skills a plus.

Strong communication and presentation skills a plus.Medpace Overview

Medpace is a full-service clinical contract research organization (CRO) providing phase l-lV clinical development services to the biotechnology, pharmaceutical, and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through the advancement of clinical research. We leverage in-country regulatory and therapeutic expertise across all major therapeutic areas including oncology, cardiology, metabolic, endocrinology, central nervous system, and anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, we employ more than 6,500 people across 40+ countries.

Medpace is a full-service clinical contract research organization (CRO) providing phase l-lV clinical development services to the biotechnology, pharmaceutical, and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through the advancement of clinical research. We leverage in-country regulatory and therapeutic expertise across all major therapeutic areas including oncology, cardiology, metabolic, endocrinology, central nervous system, and anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, we employ more than 6,500 people across 40+ countries.Why Medpace?

When you join Medpace, you become part of an innovative team that brings cutting-edge therapies to market while building a meaningful and rewarding career focused on scientific excellence and improving patient outcomes around the world through continuous learning and cross-functional collaboration.

When you join Medpace, you become part of an innovative team that brings cutting-edge therapies to market while building a meaningful and rewarding career focused on scientific excellence and improving patient outcomes around the world through continuous learning and cross-functional collaboration.

Purpose-Driven Work

Purpose-Driven WorkPurpose-Driven Work

• Work alongside physicians, scientists, and industry-leading experts committed to advancing the global development of medical therapeutics through clinical research excellence
• Work alongside physicians, scientists, and industry-leading experts committed to advancing the global development of medical therapeutics through clinical research excellence

Work alongside physicians, scientists, and industry-leading experts committed to advancing the global development of medical therapeutics through clinical research excellence

Collaborative Culture

Collaborative CultureCollaborative Culture

• Contribute to an interactive team environment that empowers decision making, creative thinking, and continuous learning through open communication and mutual trust.Leadership throughout Medpace is both accessible and approachable
• Contribute to an interactive team environment that empowers decision making, creative thinking, and continuous learning through open communication and mutual trust.

Contribute to an interactive team environment that empowers decision making, creative thinking, and continuous learning through open communication and mutual trust.

• Leadership throughout Medpace is both accessible and approachable

Leadership throughout Medpace is both accessible and approachable

Continuous Growth & Development

Continuous Growth & DevelopmentContinuous Growth & Development

• Office based environment with on-site mentorsDefined career paths with clear advancement opportunitiesIndustry renowned onboarding and training programs designed to accelerate professional developmentOngoing training and continuous learning opportunities throughout your careerAn environment that encourages employees to influence change, contribute ideas, and grow quickly
• Office based environment with on-site mentors

Office based environment with on-site mentors

• Defined career paths with clear advancement opportunities

Defined career paths with clear advancement opportunities

• Industry renowned onboarding and training programs designed to accelerate professional development

Industry renowned onboarding and training programs designed to accelerate professional development

• Ongoing training and continuous learning opportunities throughout your career

Ongoing training and continuous learning opportunities throughout your career

• An environment that encourages employees to influence change, contribute ideas, and grow quickly

An environment that encourages employees to influence change, contribute ideas, and grow quickly

Other Employee Benefits

Other Employee BenefitsOther Employee Benefits

• Competitive compensation programs that recognize and reward performanceComprehensive health, wellness, retirement, and PTO benefitsOffice based culture with occasional WFH that provides flexibility for eligible positions after trainingCompany-sponsored social events
• Competitive compensation programs that recognize and reward performance

Competitive compensation programs that recognize and reward performance

• Comprehensive health, wellness, retirement, and PTO benefits

Comprehensive health, wellness, retirement, and PTO benefits

• Office based culture with occasional WFH that provides flexibility for eligible positions after training

Office based culture with occasional WFH that provides flexibility for eligible positions after training

• Company-sponsored social events

Company-sponsored social events

Please note benefits may vary based on country.

Please note benefits may vary based on country.

What to Expect Next

What to Expect NextWhat to Expect Next

A Medpace team member will review your application and if your profile matches our current needs, you will be contacted for an interview. While we review all applications carefully, we are unable to respond to every applicant, and only candidates selected for interviews will be contacted.

A Medpace team member will review your application and if your profile matches our current needs, you will be contacted for an interview. While we review all applications carefully, we are unable to respond to every applicant, and only candidates selected for interviews will be contacted.

This job is curated by Lifelancer.

This job is curated by Lifelancer.

Lifelancer is a talent-hiring platform in Life Sciences, Pharma and IT. The platform connects talent with opportunities in pharma, biotech, health sciences, healthtech and IT domains.

Lifelancer is a talent-hiring platform in Life Sciences, Pharma and IT. The platform connects talent with opportunities in pharma, biotech, health sciences, healthtech and IT domains.

Please apply via Lifelancer platform to get connected to the application page and to find similar roles.

Please apply via Lifelancer platform to get connected to the application page and to find similar roles.