Freelance SSU / Study Start Up Opportunity - Turkey / remote

Location
Turkey (TR)
Salary
competitive pay rate
Posted
23 Apr 2021
Closes
23 May 2021
Ref
SAMSSU2304
Hours
Full Time
Contract Type
Contract
Experience Level
Experienced (non-manager)

RESPONSIBILITIES


•    Responsible for the quality deliverables at the country level; follows project requirements and applicable country rules, with moderate oversight from the SSU Country Manager.  
•    Works within the forecasted submission/approval timelines and ensures they are complied with and tracks milestone progress in agreed upon SSU tracking system in real time; if forecasted timelines are not reached:  investigates and provides clear rationale for delays, provides support on contingency plan to mitigate impact, and escalates the issue as soon as identified.  
•    Monitors basic financial aspects of the project and the number of hours/tasks available per contract; escalates discrepancies in a timely fashion.  
•    Reviews and complies with Standard Operating Procedures (SOPs) and Work Instructions (WI) in a timely manner, keeps training records updated accordingly and ensures timesheet compliance.  
•    Supports continuous improvement of quality in all Site Start-Up (SSU) components at the country level where assigned (submissions, essential document collection, communication to Competent Authorities and ECs, etc.). 
•    Ensure all relevant documents are submitted to the Trial Master File (TMF) as per Company SOP/Sponsor requirements. 
•    Local Submissions Specialist - Follows the project direction provided by the designated country start-up advisor (CSA) and SSUL.  May serve as a point of contact for the PM/SSUL (or designee) during start-up on allocated projects.  Complies and/or reviews essential document packages for site activation and may also be involved in essential document collection from site.  Prepares and submits Central EC Applications, Local EC Applications, RA Applications, and other local regulatory authorities or hospital approval submissions as required.  
•    Prepares ongoing submissions, amendments, and periodic notifications required by central and local EC and RA and other local regulatory authorities as needed within the country; includes safety notifications as required by local rules, with moderate oversight from the SSU Country Manager.
•    Country Start-Up Advisor - Acts as Subject Matter Advisor for in-country performance within the Site Start-Up.  Supports country-level intelligence on start-up (SU) and clinical trial regulatory (CTR).  Ensures that local country regulatory intelligence, as it pertains to the activities of the local SU and CTR team, is maintained on the central repository, e.g., Competent Authority submissions, EC submissions, notifications to data protection authorities, notifications/applications to any other local/federal/national body, and import/export license applications where these are obtained with RA applications.  In absence of legal advisor or dedicated subject matter may provide support for data protection at the country and provide guidance at a country level on data protection statements that need to be included on those documents which the Sponsor has contracted to the Company start-up group to adapt to local requirements.  This may include the Principal Investigator/Informed Consent and the Confidential Disclosure Agreement/contract template.  Provides input in local SOPs and WI.   Supports the creation of internal training materials on local legislation requirements.  Provides input to the team to assist with EC or CA issue resolution at the country level.  
•    Local Site ID and Feasibility Support – Provides support with site selection lead and PM/SSUL to ensure that the appropriate sites are selected for individual studies based on the requirements of the clinical trial.  
•    Local Investigator Contract and Budget Negotiator

DURATION

6-12 month contract

SALARY

Competitive pay rate

LOCATION

Homebased in Turkey

ABOUT PLANET PHARMA

Planet Pharma is an American parented Employment Business/Agency that provides global staffing services with its head-quarters in Chicago and our EMEA regional office located in Central London. We have invested significantly in creating a robust international platform that enables us to work compliantly in 30+ countries with a current network of 2500+ active contractors globally as well as a very strong permanent / direct hire recruitment offering.

Our specialist knowledge and close relationships with our clients and the wider industry really makes us unique in our field. Just recently we were recognised by FORBES as the 17th best professional staffing firm, and have won multiple awards from industry accredited bodies for our commitment to excellence and service delivery. We have extensive functional expertise including: Regulatory Affairs, Pharmacovigilance, QA, QC, Submissions experts, Clinical development, Quality, Biostatistics, and Medical Affairs / Writing.

We are an equal opportunities Recruitment Business and Agency. We welcome applications from all suitably qualified candidates regardless of their race, sex, disability, religion/belief, sexual orientation or age.

www.planet-pharma.com

TO APPLY

Please click ‘apply’ or contact Sam Chapple at Planet Pharma for more information:

E: schapple@planet-pharma.co.uk

T: +44(0)203 868 8607

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