Clinical Research Coordinator Q-Max Clinical Research
Q-Max Clinical Research
Office Location
Full Time
Experience: 2 - 2 years required
Pay:
Salary Information not included
Type: Full Time
Location: Gujarat
Skills: informed consent, Clinical Research, Communication, Interpersonal Skills, Teamwork, Protocol management, Coordinating Clinical Trials, Attention to Detail, Organizational Skills
About Q-Max Clinical Research
Job Description
You will be joining Q-Max Clinical Research Services as a Clinical Research Coordinator at their Nadiad location. Your primary responsibilities will include managing tasks related to informed consent, protocol management, research coordination, and supporting clinical trials. To excel in this role, you should possess skills in informed consent and protocol management, along with previous experience in clinical research and coordinating clinical trials. Attention to detail and strong organizational skills are crucial for success in this position. Additionally, effective communication, excellent interpersonal skills, and the ability to work collaboratively in a team environment are essential. Ideal candidates for this role will hold a Bachelor's or Master's degree in a relevant field such as Life Sciences or Health Sciences. Certification in Clinical Research would be considered a valuable advantage. If you are seeking a challenging opportunity to contribute to successful drug development outcomes and work in a dynamic environment, this role at Q-Max Clinical Research Services may be the perfect fit for you.,