Careers

 

 

As ClinMed Pharma looks to expand, we are currently recruiting for the following position:

 

CLINICAL RESEARCH ASSOCIATE

We care about our people as they are the key to our success. We provide an open and friendly work environment. We empower people and provide them with opportunities to develop their long term career. You will work in experienced and friendly team of professionals working within international projects in wide variety of therapeutic indications.

Responsibilities:

  • Conduct of all types of site visits in accordance with the protocol, Standard Operating Procedures (SOPs), Good Clinical Practice (GCP) and the applicable regulatory requirements
  • Communication with sponsor, investigators, vendors
  • Maintenance of appropriate documentation regarding clinical site management
  • Quality control, preparation for and attendance at company’s audits
  • Training of investigators and clinical trial team members

Requirements:

  • Medical or life science education (pharmacy, medicine, biology or similar)
  • Knowledge of ICH-GCP guidelines
  • Good English skills, both spoken and written
  • Excellent communication and interpersonal skills
  • Good computer handling skill
  • Desire and ability to travel
  • Previous experience in clinical trials appreciated

 

If you would like to forward your CV to us with a covering email to click to view, we may consider you for any future opportunities within our company

 


 

CLINICAL TRIAL ADMINISTRATOR BASED IN WARSAW, POLAND

 

Responsibilities

  • Support the company team in the preparation, handling, distribution, filing, and archiving of clinical documentation and reports according to the scope of work and standard operating procedures.
  • Support in Clinical Trial Application submission and translation of project specific documents.
  • Act as a central contact for the clinical team for project communications, correspondence and associated documentation.
  • Assist with preparation, handling and distribution of Clinical Trial Supplies and maintenance of tracking information.
  • Assist with the tracking and management of Case Report Forms (CRFs) and queries
  • Accompany CRAs on site visits to assist with clinical monitoring duties upon completion of required training and with required approval.

Requirements:

  • Medical or life science education (pharmacy, medicine, biology or similar)
  • At least 1 year experience in clinical trials
  • Fluent English skills, both spoken and written
  • Good computer handling skill (MS Outlook, Word, Excel, PowerPoint)
  • Excellent communication and interpersonal skills
  • Multitasking, ability to set priority,
  • A strong knowledge of GCP and understanding of the clinical trials environment along the regulatory requirements
  • Ability to travel; driving license

 

 

If you would like to forward your CV to us with a covering email to click to view, we may consider you for any future opportunities within our company