Medpace is Hiring for Clinical Research Associate Position

Hello friends there is golden opportunity for you if you are done your graduate degree in Life science or pharmacy.Medpace is Hiring for Clinical Research Associate.This is the best job for you and herer you will det a massive salary of 4 lakh per year.And the location of the job is Navi Mumbai so if you are intrested in this job then read the details below and apply ASAP.

About Company

Medpace is a company that helps biotech, pharmaceutical, and medical device industries with clinical research. Medpace goal is to speed up the global development of safe and effective medical treatments. Medpace have experts in local regulations and various medical fields like cancer, heart disease, and more. Based in Cincinnati, Ohio, we have over 4,000 employees in nearly 40 countries.

Medpace Hiring 2024

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MEDPACE CRA TRAINING PROGRAM
You don’t need any research experience because Medpace is offering thorough initial and
continuous training that surpasses what other CROs provide. Join MEDPACE PACE Training
Program to become part of a group of Professionals Achieving CRA Excellence.

1. PACE equips you with the necessary tools to confidently carry out your duties and
   enhance your abilities as a Medpace CRA.
2. You can supplement your in-house and field training with additional clinical
   research departmental core rotations to gain insights into drug and device
   development processes
3. Through interactive discussions and hands-on exercises, PACE® develops your CRA
   skills effectively.

Job Overview

1. Communicate with site staff, verify investigator qualifications and resources.
2. Review medical records and research data for accuracy
3. Monitor subject eligibility and regulatory documents.
4. Conduct visits to research sites to ensure compliance with protocols
5. Assess patient recruitment success and prepare detailed monitoring reports for compliance.
6. Track investigational product inventory and adverse events.

Job Description

1. Communicate with medical staff at sites, including coordinators and research doctors.
2. Check and review adverse events, serious issues, medications taken alongside the study drugs, and related illnesses to ensure accurate reporting.
3. Conduct visits to research sites to ensure they follow the approved plan for starting,monitoring, and finishing studies.
4. Track medical devices or experimental drugs, making sure they are used correctly and accounted for.
5. Evaluate how well research sites are recruiting and keeping patients, suggesting improvements.
6. Review regulatory documents.
7. Verify medical records and research documents to match the data in case reports, correcting errors and following rules for good documentation.
8. Write reports after monitoring visits, highlighting key findings, issues, and actions needed to follow the rules.
9. Ensure only eligible subjects are enrolled by investigators.
10. Check that investigators have the right qualifications, training, and resources, like labs and equipment.

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Job Responsibilities

1. Talk to medical staff at sites, including coordinators and research doctors.
2. Visit research sites to make sure they follow approved plans for starting, monitoring,and finishing studies.
3. Verify medical records and research documents to match data in reports, fixing errors and following documentation rules.
4. Review serious events, medications used with study drugs, and related illnesses for accurate reporting
5. Examine regulatory documents.
6. Monitor medical devices or experimental drugs to ensure proper use and tracking.
7. Check investigators have needed qualifications, training, and resources such as labs and equipment.
8. Confirm investigators enroll only eligible subjects.
9. Write reports after visits, highlighting important findings, issues, and actions needed to follow rules.
10. Assess how well research sites recruit and keep patients, suggesting ways to improve.

Skills Required For the Position

1. Good Communication Skills
2. Time Management Skills
3. Adaptibility Skills
4. Critical Thinking

Qualifications Required for this Position

1. Minimum of a bachelor’s degree;  Health or life science related field preferred
2. Candidate with Clinical Research Coordinator experience is an advantage
3. Willing to travel approximately 60-80% nationally
4. Familiarity with Microsoft® Office
5. Strong communication and presentation skills a plus.

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:

1. Dynamic working environment, with varying responsibilities day-to day
2. Expansive experience in multiple therapeutic areas
3. Work within a team of therapeutic and regulatory experts
4. Defined CRA promotion and growth ladder with potential for mentoring and management advancements
5. Competitive pay and opportunity for significant travel bonus

How To Apply

Intrested candidate needs to apply on the given link below

Apply Link : Click Here