Associate Clinical Research Associate

October 4, 2024

Company: Merck

Industry: Private

Employment Type:- Full Time

Work Hours:- 8 Hours

Locations:- USA

Full Job Description:-

We are seeking an enthusiastic and highly motivated Associate Clinical Research Associate to join our team at Merck & Co. In this role, you will have the opportunity to work on cutting-edge clinical research projects and contribute to the development of life-changing medicines. As an Associate Clinical Research Associate, you will support the planning, implementation, and management of clinical trials, ensuring the safety and well-being of study participants. We are looking for individuals with a strong background in life sciences and a passion for making a positive impact on patients' lives. If you are a detail-oriented team player with excellent communication and organizational skills, we encourage you to apply for this exciting opportunity.

Support the planning, implementation, and management of clinical trials in accordance with company and regulatory guidelines.
Monitor and ensure the safety and well-being of study participants throughout the duration of the trial.
Conduct data collection, analysis, and interpretation to contribute to the development of life-changing medicines.
Collaborate with cross-functional teams including physicians, scientists, and study coordinators to ensure successful trial execution.
Maintain accurate and organized study documentation, including study protocols, informed consent forms, and regulatory submissions.
Assist in the preparation and presentation of study results to internal and external stakeholders.
Adhere to all applicable regulations, guidelines, and company policies.
Proactively identify and communicate potential risks and issues to the study team.
Contribute to the development and implementation of standard operating procedures and best practices.
Continuously seek opportunities for improvement and suggest innovative solutions to enhance study processes.
Stay up-to-date with advancements in the field of life sciences and contribute knowledge to the study team.
Represent the company in a professional and ethical manner at all times.
Train and mentor new team members as needed.
Act as a liaison between the study team and study sites to ensure timely and accurate communication.
Handle any other responsibilities as assigned by the Clinical Research Manager.

Job Qualifications

Strong Communication And Organizational Skills
Bachelor's Degree In A Relevant Scientific Field Such As Biology, Chemistry, Or Pharmacy
Minimum Of 1-2 Years Of Experience In Clinical Research Or A Related Field
Knowledge Of Fda Regulations And Good Clinical Practice (Gcp) Guidelines
Ability To Work Independently And In A Team Environment, With A High Attention To Detail And The Ability To Manage Multiple Tasks Simultaneously.

Required Skills

Data Management
Quality Control
Data collection
Regulatory compliance
Clinical monitoring
Study Coordination
Protocol Adherence
Ad
Subject Recruitment
Study Documentation
Investigator Training
Study Timelines

Soft Skills

Communication
Conflict Resolution
Emotional Intelligence
Leadership
Time management
Organization
flexibility
Teamwork
Adaptability
Problem-Solving