work with us

Creative Pharma & HR Services S.M.S.A. is a customer-oriented Contract Research Organization offering services to the Pharmaceutical, Biotechnology and Medical Devices Industry. Our mission is to meet customer needs while maintaining strict confidentiality and professionalism.

The quality of our people is the cornerstone of Creative Pharma Services. Our Team consists of passionate, outcome-oriented, innovative, enthusiastic and with outstanding academic background people and that is our greatest asset. Due to our constant growth, we are currently seeking for the following positions.

If you are interested in, please send us your CV to: career@creativephs.com

Main Responsibilities

The job holder will be responsible for the administration and coordination of all activities related to the aspects of study start up routine and furthermore the support of the Clinical Study team.

More specifically:

  • Provide administrative support to the Project team in accordance with ICH, GCPs and respective SOPs.
  • Collection and preparation of essential documents.
  • Contact with investigative sites during site start-up activities.
  • Working with investigative sites to collect the required investigator and regulatory documents for a study.
  • Prepare submission packages for Local and/ or Central IRB /IEC and Regulatory Authorities.
Requirements
  • A Bachelor’s Degree in Health Sciences or Business Administration.
  • Minimum 2 years of professional experience in a Clinical department as a Start Up Specialist.
  • Knowledge of contract handling and clinical terminology.
  • Familiarity with ICH-GCP guidelines.
  • Technology savvy and pc literacy is a must
  • Fluency in written and oral English
  • Essential personality attributes: multi-tasker with the ability to prioritize, ability to work in a fast-paced team, attention to detail, ability to handle pressure and tight deadlines.
What we offer

Creative Pharma Services is offering a competitive remuneration package according the Industry’s standards. Nonetheless, we are also proud at Creative Pharma Services that we are an open and learning organization that fosters a collaborative, enthusiastic, fast paced working environment, but also an employer that invests in people’s potential and growth.

All applications will be treated fairly and with strict confidentiality.

Main Responsibilities

The job holder (CTA) will be responsible for the administration and coordination of all activities related to the aspects of Clinical Trails and furthermore the support of the Clinical team.

More specifically:

  • Provides administrative support to the Project team in accordance with ICH, GCPs and respective SOPs
  • Performs the creation, review and submission of clinical trial protocol, amendments and reports
  • Maintains and updates all related databases
  • Assists in the production of study reports and updates
  • Prepares investigator budget allocation and payments
  • Maintains the Trial Master Files up to date with all related study documents
Requirements
  • A Bachelor’s Degree in Natural Sciences
  • Minimum 1 year of professional experience in a Clinical department
  • Knowledge of contract handling will be highly considered
  • Familiarity with ICH-GCP guidelines
  • Technology savvy and pc literacy is a must
  • Fluency in written and oral English
  • Essential personality attributes: multi-tasker with the ability to prioritize, ability to work in a fast-paced team, attention to detail, ability to handle pressure and tight deadlines.
What we offer

Creative Pharma Services is offering a competitive remuneration package according the Industry’s standards. Nonetheless, we are also proud at Creative Pharma Services that we arean open and learning organization that fosters a collaborative, enthusiastic, fast paced working environment, but also an employer that invests in people’s potential and growth.

All applications will be treated fairly and with strict confidentiality.

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