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
Associate Clinical Research Associate
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