Overview
Our client, a leading organization in the pharmaceutical and clinical research industry, is seeking a dedicated Assoc Med Director to join their team. As an Assoc Med Director, you will be an integral part of the Medical Affairs department supporting clinical trial activities and safety monitoring with a focus in Rheumatology. The ideal candidate will demonstrate strong therapeutic expertise, excellent communication skills, and a proactive approach to problem-solving, which will align successfully within the organization. Job Title:
Assoc Med Director Location:
Cambridge, MA (Remote work available) Pay Range:
120-150/hr on W2
Responsibilities
Provide medical oversight of clinical trials to ensure compliance with SOPs, client directives, good clinical practice, and regulatory standards. Attend and present at investigator and sponsor meetings, offering medical consultation to clients, investigators, and project teams. Support business development activities through medical expertise and strategic input. Review and analyze serious adverse events, marketed product reports, and other safety-related deliverables ensuring accuracy and regulatory compliance. Manage all medical aspects of contracted tasks across the pharmaceutical product lifecycle, including safety monitoring and signal detection activities. Qualifications
MD board certification in Rheumatology or related specialty. Clinical experience in treating patients within the specialty or relevant industry experience in clinical trials or safety/Pharmacovigilance. Strong decision-making, organizational, and analytical skills. Excellent oral and written communication skills, with fluency in English. Working knowledge of safety databases (e.g., MedDRA), GCP, FDA, ICH, EMA guidelines, and biostatistics. Benefits
Opportunity to work remotely with flexible scheduling options. Engage in meaningful projects that impact patient safety and drug development. Collaborate with a diverse and innovative team of professionals. Enhance your expertise in clinical safety and pharmacovigilance. Contribute to advancing healthcare through your medical expertise. Upon completion of waiting period consultants are eligible for: Medical and Prescription Drug Plans Dental Plan Vision Plan Health Savings Account Health Flexible Spending Account Dependent Care Flexible Spending Account Supplemental Life Insurance Short Term and Long Term Disability Insurance Business Travel Insurance 401(k), Plus Match Weekly Pay
#J-18808-Ljbffr
Our client, a leading organization in the pharmaceutical and clinical research industry, is seeking a dedicated Assoc Med Director to join their team. As an Assoc Med Director, you will be an integral part of the Medical Affairs department supporting clinical trial activities and safety monitoring with a focus in Rheumatology. The ideal candidate will demonstrate strong therapeutic expertise, excellent communication skills, and a proactive approach to problem-solving, which will align successfully within the organization. Job Title:
Assoc Med Director Location:
Cambridge, MA (Remote work available) Pay Range:
120-150/hr on W2
Responsibilities
Provide medical oversight of clinical trials to ensure compliance with SOPs, client directives, good clinical practice, and regulatory standards. Attend and present at investigator and sponsor meetings, offering medical consultation to clients, investigators, and project teams. Support business development activities through medical expertise and strategic input. Review and analyze serious adverse events, marketed product reports, and other safety-related deliverables ensuring accuracy and regulatory compliance. Manage all medical aspects of contracted tasks across the pharmaceutical product lifecycle, including safety monitoring and signal detection activities. Qualifications
MD board certification in Rheumatology or related specialty. Clinical experience in treating patients within the specialty or relevant industry experience in clinical trials or safety/Pharmacovigilance. Strong decision-making, organizational, and analytical skills. Excellent oral and written communication skills, with fluency in English. Working knowledge of safety databases (e.g., MedDRA), GCP, FDA, ICH, EMA guidelines, and biostatistics. Benefits
Opportunity to work remotely with flexible scheduling options. Engage in meaningful projects that impact patient safety and drug development. Collaborate with a diverse and innovative team of professionals. Enhance your expertise in clinical safety and pharmacovigilance. Contribute to advancing healthcare through your medical expertise. Upon completion of waiting period consultants are eligible for: Medical and Prescription Drug Plans Dental Plan Vision Plan Health Savings Account Health Flexible Spending Account Dependent Care Flexible Spending Account Supplemental Life Insurance Short Term and Long Term Disability Insurance Business Travel Insurance 401(k), Plus Match Weekly Pay
#J-18808-Ljbffr